- Research article
- Open Access
Differentiation in the genetic basis of stem trichome development between cultivated tetraploid cotton species
BMC Plant Biology volume 21, Article number: 115 (2021)
Cotton stem trichomes and seed fibers are each single celled structures formed by protrusions of epidermal cells, and were found sharing the overlapping molecular mechanism. Compared with fibers, cotton stem trichomes are more easily observed, but the molecular mechanisms underlying their development are still poorly understood.
In this study, Gossypium hirsutum (Gh) and G. barbadense (Gb) were found to differ greatly in percentages of varieties/accessions with glabrous stems and in trichome density, length, and number per trichopore. Gh varieties normally had long singular and clustered trichomes, while Gb varieties had short clustered trichomes. Genetic mapping using five F2 populations from crosses between glabrous varieties and those with different types of stem trichomes revealed that much variation among stem trichome phenotypes could be accounted for by different combinations of genes/alleles on Chr. 06 and Chr. 24. The twenty- six F1 generations from crosses between varieties with different types of trichomes had varied phenotypes, further suggesting that the trichomes of tetraploid cotton were controlled by different genes/alleles. Compared to modern varieties, a greater proportion of Gh wild accessions were glabrous or had shorter and denser trichomes; whereas a smaller proportion of Gb primitive accessions had glabrous stems. A close correlation between fuzz fiber number and stem trichome density was observed in both Gh and Gb primitive accessions and modern varieties.
Based on these findings, we hypothesize that stem trichomes evolved in parallel with seed fibers during the domestication of cultivated tetraploid cotton. In addition, the current results illustrated that stem trichome can be used as a morphological index of fiber quality in cotton conventional breeding.
Plant trichomes are epidermal cell outgrowths that perform a variety of important functions. There are many types of trichomes, which are characterized by their morphology, location, and nature. Trichomes can be unicellular or multicellular, glandular or non-glandular, and branched or unbranched. Moreover, branched hairs can be dendritic, tufted, or stellate. Plants with trichomes tend to be more resistant to abiotic stresses, such as frost, heat or drought. Although the functions of trichomes are not clear, they are generally believed to provide physical protection to terrestrial plants against insects, pathogens, and herbivores .
Their easy manipulation and observation made plant trichomes ideal for studying cell differentiation-related pathways [2, 3]. The trichomes of Arabidopsis thaliana have a specialized unicellular structure and are 200–500 μm in length. In Arabidopsis, trichome development shares common mechanisms with root epidermal development, each involving closely-related cell fate transcription factors and a similar lateral inhibitive signaling pathway . The process of trichome initiation includes three physiological stages: endore duplication, rapid growth, and branch formation. The regulatory genes and functions of encoded proteins were investigated to determine mechanisms controlling Arabidopsis trichome initiation and the early stages of morphogenesis [5, 6]. The key initiation genes encode a MYB, a bHLH, and a WD-40 repeat-containing protein, forming a MYB–bHLH–WD40 complex that effects trichome initiation as a dual regulator , while CAPRICE and TRIPTYCHON negatively regulate trichome initiation . Tobacco (Nicotiana tabacum L.) leaf epidermal trichomes differ from those of Arabidopsis in that they are multicellular. The mechanisms of tobacco trichome formation have both similarities and differences from those of Arabidopsis unicellular trichomes, both being controlled by the MYB–bHLH–WD40 regulatory mechanisms, but differing in the functions of the MYB genes .
Cotton fiber is the most important raw material in the textile industry, and cotton seeds contain high oil and protein contents that are consumed by animals and humans . Cotton fibers are single-celled structures originating from the ovular epidermis, while trichomes originate from aerial epidermis [2, 11], each by similar developmental processes . Trichomes are broadly classified into glandular and non-glandular forms, and their morphology has been described in detail by Turley et al. (2012).
Classical genetic studies revealed that cotton trichome growth is affected by many loci, which were classified into groupst1 to t5 [13, 14]. Wright et al. (1999) mapped five quantitative trait loci (QTLs) for leaf and stem trichomes using an F2 population derived from a cross between Gossypium hirsutum (Gh) and G. barbadense (Gb) varieties, including a leaf pubescence QTL on Chr. 06 that corresponds to the t1 locus (Kloth 1993), three other leaf pubescence QTLs on Chrs. 01, 07, and 25, and a QTL on Chr. 23 that is associated with stem trichome density. The latter four QTLs were hypothesized to correspond to the t2 to t5 loci . Lacape and Nguyen (2005) also confirmed the location of locus t1, which is a major determinant of leaf pubescence, in the central region of Chr. 06, and additional genes located on seven other chromosomal locations either positively or negatively affect trichome density. In addition, QTLs affecting lint percentage, fiber length, fiber length uniformity and fiber strength were identified in the t1 locus region of Chr. 06, suggesting that this locus also affects cotton fiber quality . In G. arboreum, the glabrous mutation was mapped to linkage group A3, which appears to be orthologous to the t1 locus of allotetraploids . A fiber mutation locus, sma-4 (ha), was detected in the same F2 population that co-segregated with the glabrous stem, which suggests either a close linkage or common genetic control between lint fibers and leaf/stem trichomes [17, 18].
Gh and Gb, the two major species used in cotton production, originated from natural hybridization between species resembling G. raimondii, the diploid D genome donor, and G. arboreum, the diploid A genome donor, an estimated 1–1.5 million years ago . These cultivated tetraploid species display considerable differences in stem trichome morphology, which suggests that they experienced different evolutionary processes, as also indicated by changes in chromosome structure and gene content revealed by re-sequencing of their whole genomes . Although several studies have reported QTL mapping of cotton trichomes and cloning of a few critical genes [15, 16, 21, 22], the mechanisms governing trichome initiation at the molecular level are still unclear. In this paper, we report the classification of stem trichomes, molecular mapping of their underlying genes, and association analysis between the amount of fuzz fiber and stem trichome density. We also discuss possible evolutionary processes that may have influenced the genetic basis of trichome growth during speciation and domestication of tetraploid cotton.
Inter-specific and intra-specific variations in the stem trichome phenotypes of two cultivated tetraploid cottons
There were two kinds of trichomes grown from trichopores, single and tufted/complex dendritic, as seen under a stereo microscope (Fig. 1), and they are similar to those from leaves . The single trichomes were normally long and thin with sharp ends, while the tufted trichomes were normally shorter and grew from the same trichopore. The trichome numbers per trichopore varied from two to more than 10. Different cotton plants, even from the same species, differed in trichome number per trichopore, trichome density, and trichome length, forming clearly different trichome phenotypes. Stem trichome densities were grouped into six classes (0–5) from none to pilose (Fig. S2). As a whole, the cotton stem trichomes were categorized into four types (I–IV) (Table 1, Fig. 2). In Type I, most were singular long trichomes per trichopore, plus a few clusters, and the trichome density differed among different varieties. The stems with low trichome density levels (grades 1 and 2) were further classified as Type Ia and those with high trichome density (grade 4) as Type Ib. In Type II, both singular and clustered trichomes occurred. Trichomes were shorter and coarser than those in Type I, with higher density resulting in a pilose phenotype over the whole plant. In Type III, multiple trichomes formed clusters from one trichopore. They grew sparsely on stems and were shorter than those of Type II. In Type IV, the tufted/complex dendritic trichomes were extremely short and dense, looking as if they were covered by a layer of powder.
The trichome phenotypic data of 11,442 Gh and 4323 Gb varieties/accessions were downloaded from the USDA National Cotton Germplasm Collection, one of the largest collections of cotton germplasm resources  (Table S6), and used to determine the percentages of cultivars having different stem trichome densities. The two species differed significantly in the proportions of glabrous varieties (Fig. 3a). In total, 55.4% of the Gb varieties (accessions) did not grow or had very few trichomes on their stems, while 97% of the Gh varieties had trichomes in grades 1–5, and only 3% had glabrous stems. In addition, the two cultivated tetraploid cottons were clearly different in all aspects of the trichome phenotype. Type I was the main type on Gh stems, accounting for 95% (Table 1, Fig. 2), while Type III was the main type on Gb stems, accounting for 31.4%. In addition, 5.6% of Gb varieties had Type IV trichomes (grades 4 and 5), while less than 1% of Gh had Type II trichomes (grades 4 and 5). Similar results were obtained from 295 Gh and 246 Gb varieties (Table 2, Fig. 3b, Table S1 and S4). Therefore, the two cultivated species had distinctive stem trichome phenotypes, especially their trichome density levels and trichome types.
Wild G. hirsutum accessions differed significantly in stem trichome morphology from modern cultivated varieties
We observed the stem trichome phenotypes of wild Gh accessions planted in Hainan, China (Table S2) and found significant differences between wild forms and modern varieties. Compared with modern upland cotton, the wild accessions showed the following trichome characteristics (Table 2, Table S2 and Fig. S4): (1) No or fewer trichomes on stems. Among 180 wild accessions of seven wild races, 30 (16.8%) were glabrous, while only about 3% of the modern varieties in the data from the USDA National Cotton Germplasm Collection (Fig. 3) and none of the varieties we collected were glabrous (Table 2, Table S1). When stem pubescence was compared among the wild accessions based on flowering time, those that flowered later had a greater proportion of glabrous accessions than those that flowered at regular time as modern varieties. Among 81 late-flowering accessions, 37 (45.6%) were glabrous, or had grade 1 trichomes, whereas among 99 regular flowering accessions, only 19 (19.2%) were glabrous, or had grade 1 trichomes (Table 2). When different wild races were compared, race marie-galante had more glabrous accessions than the other wild races. (2) A large number of wild accessions had shorter and denser trichomes than modern varieties. Among the 149 accessions having stem trichomes, 66 (44.3%) were shorter than the Type I modern varieties, including 28 similar to Type II and 6 that were even shorter, having the pilose phenotype (Table S2, Fig. S4), especially among the morrillii race. As a whole, wild G.hirsutum accessions either have more ratio of glabrous stem, or more ratio of shorter trichome compared to modern varieties.
Stem trichome phenotypes of diploid ancestors of tetraploid cotton
To compare the stem trichome phenotypes of diploid ancestors with those of cultivated tetraploid cottons, 77 individual plants from 12 accessions of G. arboreum (Table S7) and 5 individual plants from G. raimondii were observed. All the G. raimondii plants had very short and dense clustered trichomes on their stems, similar to Gb Type IV (Fig. 4a). Compared with G. raimondii, G. arboreum had more variation in stem trichome phenotypes (Fig. 4b). As in Gh, G. arboreum accessions also had singular and clustered trichomes. However, the clustered trichomes of G. arboreum were shorter than those of Gh and even shorter than Gb Type IV. As a result, the clusters were difficult to visualize. On the basis of their growth situations, the stem trichome phenotype of G. arboreum was classified into four types: single plus cluster, only single, only cluster, and glabrous. The stem trichome phenotypes of 12 G. arboreum accessions were investigated. Six had singular and clustered trichomes, four only had clustered trichomes, one only had singular trichomes, and one had the glabrous phenotype. Two diploid ancestors differ significantly. G. raimondii has the similar stem trichome as Gb, while G. arboreum has the stem trihomce like Gh.
Genetic mapping of stem trichomes
To reveal the genetic basis regulating different types of stem trichomes, five crosses involving varieties having different types of stem trichomes were made (Table S5). Cotton stem trichome initiation is believed to be mainly controlled by genes on Chrs. 06 and 24 [15, 16, 22, 25, 26]. Therefore, our mapping efforts focused on these two genes and 77 polymorphic DNA markers, 23 on Chr. 06 and 49 on Chr. 24, among them 54 were newly developed based on reference genome sequences of G. hirsutum var. TM-1 [20, 27] (Table S8). Definitely, it is an efficient way to find the gene(s) related to trichome phenotype, but also will miss some other loci.
Type I trichomes in Gh
QF-10/1 is a Gh variety with Type Ia stem trichomes, grade 2, similar to genetic standard line TM-1. To map the genes conferring this type of stem trichome, QF-10/1 was crossed with Tu 75–37, a glabrous Gb variety. No trichomes grew on the stems of the F1 plants. An F2 population consisting of 118 plants showed continuous variation, and most of them (60%) had grade 0 or I trichome, while some had grade IV trichomes, surpassing the Gh parent (Fig. 5). Using this population, genetic maps were constructed for Chrs. 06 and 24, consisting of 18 and 24 DNA markers, respectively (Fig. 6a, b, Some co-segregation markers were not displayed in the figures. All marker information was listed in the Table S5. The trichome grade and genotypes of the F2 plants were given in Table S11). Combining the trichome phenotyping and genotyping data from this population, a QTL that had a LOD value of 4.4 and explained 18.4% of the phenotypic variation was detected in the region between NAU5433 and JESPR194 on Chr. 06, and was tightly associated with AF2, a SSCP marker developed by the GhHD1 sequence (Table 3, Fig. 6a, Table S8). Another QTL was detected in the region between D08–163 and L4–239 on Chr. 24 that had a LOD value of 8.6 and explained 30.6% of the phenotypic variation (Table 3, Fig. 6b).
Type II trichomes in Gh
Previously, we mapped the Type II stem trichomes of T586 to Chr. 06 and confirmed that its pilose phenotype was probably controlled by the HD1 gene, using an F2 population derived from the cross between T586, a typical Gh genetic standard line with grade 5 stem trichomes and Pima S6 with glabrous stems . To further clarify the genetic relationship between Type I and II stem trichomes, we crossed the Gh variety Liao1779, having a pilose morphology and grade 5 stem trichomes like T586, with Xinyan96–48, a variety having Type Ia stem trichomes (grades 1 and 2). The F1 plants had stems similar to those of Liao1779, covered with heavy trichomes. In total, 66 F2 plants showed clearly different trichome densities, most (52) having a high density of trichomes like Liao1779 (grades 4 and 5), and 11 had stem trichomes like Xinyan96–48, grades 1 and 2. Only three plants had intermediate trichome density levels (Table S9). These results indicated that the pilose stem (Type II) was probably controlled by a dominant gene. Using AF2, we found that both parents showed very good polymorphism, and the segregation of stem trichome density in this F2 population was closely correlated with the genotype of the SSCP marker (Table S9), suggesting that the pilose stem trichomes of Liao1779 were also controlled by GhAt-HD1, as in T586 .
Type III trichomes in Gb
This type had sparse clustered trichomes on the stems, grading 0 or 1. To map this type of trichome, N73DeltapineNGO, a Gh variety with glabrous stems, was crossed with VIR-59TV, a Gb variety having the typical Type III stem trichomes. The F1 did not have, or had only a few trichomes on stems, like the Gh parent. In the F2 population, most plants (86 of 130) did not have, or had only a few trichomes, like the F1 plants. Approximately 1/3 of F2 plants had stem trichomes of grade 1, and a few were graded at > 2 or 3 (Fig. 5). Thus, the glabrous stem of N73DeltapineNGO is probably controlled by a dominant gene. To map this gene, a genetic linkage map of Chr. 24, consisting of 28 markers, was constructed, and a QTL in the region between L4–211 and NAU3904 that had a LOD value of 17.6 and explained 51.5% of phenotypic variance was identified (Table 3, Fig. 6c. The trichome grade and genotypes of the F2 plants were given in Table S12).
Type IV trichomes in Gb varieties
Bazhou 03 and L-7009 had typical Type IV stem trichomes. To map the genes correlated with this phenotype, Bazhou 03 was crossed with N73DeltapineNGO. The F1 plants showed a trichome phenotype similar to that of N73DeltapineNGO. The F2 plants showed continuous segregation in trichome density, but displayed two peaks at grades 0 and 4 (Fig. 5). Among 383 F2plants, 244 (63.9%) had few trichomes, graded 0 and 1, similar to N73DeltapineNGO; and 80(20.9%) had many trichomes, graded 4, similar to Bazhou 03. Only 44 (11.5%) plants had trichomes of grade 2, and very few plants had trichomes of grade 3. When a trichome density of less or equal to grade 2 was used to form a group and a trichome density greater than grade 2 formed a second group, the ratio of the two groups of plants was close to 3:1, again suggesting that the glabrous stem trichomes of N73DeltapineNGO were probably controlled by a dominant gene. To map this gene, 21 polymorphic SSR and SSCP markers were used to genotype the F2 plants, and a linkage map covering 3.74 cM was constructed (Fig. 6d. The trichome grade and genotypes of the F2 plants were given in Table S13). A significant QTL having a LOD value of 149.1 and explaining 83.7% of the phenotype variation was detected in the region between L4–209 and T10 (Table 3, Table S8). All these mapping results strongly suggested that the gene on Chr. 24 is essential in regulating stem trichome initiation.
To reveal the genetic relationship between the Types III and IV stem trichomes of Gb varieties, Aken 4154 (Type III) was crossed with Bazhou 03 (Type IV). The F1 plants showed a trichome phenotype similar to that of Aken 4154, with a few clustered trichomes, and some had almost no trichomes. Like the (Bazhou 03 x N73DeltapineNGO)F2 population, this F2 population showed clear segregation in stem trichome density (Table S10). Among 64 F2 plants, 44 had stem trichomes of grades 0 and 1, whereas 18 had stem trichomes of grades 3 and 4, and only two had trichomes of grade 2. This result again suggests that the pilose phenotype of Bazhou 03 was controlled by a recessive gene. A polymorphic SSR marker (D08–98, Table S8) which had a very close correlation with stem trichome phenotype (Fig. 6c) was used to genotype the F2 plants, also revealing a close correlation with stem trichome density, with only three exceptions (Table S10), suggesting that Types III and IV stem trichomes in Gb were controlled by the same gene but different alleles, and that Type III was dominant to Type IV. Above mapping efforts revealed that the different types of Gh and Gb stem trichome were mainly controlled by different combinations of genes or alleles on Chr.06 and 24. The one on Chr.24 probably plays even more important function compared to one on Chr.06, especially in Gb.
Inter-specific and intra-specific variations in stem trichome phenotypes are reflected in F1 hybrids of crosses between Gh and Gb varieties having different types of stem trichomes
To further clarify the classification of stem trichomes, more inter-specific crosses between Gh and Gb varieties with different types of stem trichomes were performed (Table 4). Interestingly, when Gh and Gb varieties having the same type of stem trichomes were crossed, the F1 hybrids always showed a similar stem trichome morphology (Table 4, Fig.S5). However, F1 plants from crosses between Gh and Gb varieties with different types of stem trichomes always displayed different stem trichomes (Table 4, Fig.S5). For example, when Gh varieties with Type Ia stem trichomes were crossed with Gb variety H7124, a representative of the glabrous varieties, the F1 hybrids did not grow trichomes on their stems. However, when these Gh varieties were crossed with Aken 4154 or L-7009, representatives of Gb varieties with Types III and IV stem trichomes, respectively, the resultant F1 always had stem trichome phenotypes close to Types III and II, respectively (Table 4, Fig.S5). These results suggested that the stem trichome alleles in Gb are dominant to those of Gh Type Ia trichomes, except for those responsible for the lengths of the F1 hybrids of Type I × Type IV, which were intermediate between the two parents. When three Gh varieties with Type Ib stem trichomes were crossed independently with the above three Gb varieties, most of the F1 plants showed different stem phenotypes from the above crosses with the same Gb varieties. When Gh varieties with Type II trichomes were crossed with H7124 and L-7009, the F1 plants had a stem trichome phenotype similar to Type II of Gh, indicating that Gh trichome genes are dominant to those of Gb. These results further confirmed that classification of stem trichome established in this study was correct and can be further used in gene cloning and cotton breeding.
Stem trichome density is closely related to fiber initiation and development in both G. hirsutum and G. barbadense
We analyzed the correlation between the densities of fuzz fibers and stem trichomes. First, we examined the fuzz fibers of Gh wild species, which showed significant differences in stem trichome phenotypes compared with modern varieties. A much greater proportion of them had no or fewer fuzz fibers than the modern varieties (~ 27% vs 1.4%, Table 2, Table S2), which suggested a correlation with trichome density. In addition, more wild species had shorter and denser stem trichomes than modern varieties, which was also in accordance with fiber length, because most wild Gh accessions have very short lint fibers. Thus, fuzzy/lint fibers and stem trichomes may have at least partly overlapping genetic bases for regulating their initiation and development.
To further investigate the relationship between stem trichomes and fiber densities, we observed the stem trichomes of 37 Gh fuzzless mutants and found that there was a much higher percentage of the mutants having no or few trichomes (grades 0 and 1) than in the common varieties (56.8% vs 3.7%) (Table 2, Table S3). Only 11% of the fuzzless mutants had denser trichomes (grades 3 and 4), compared with the common varieties (78%).
As indicated above, most Gb varieties did not have, or had very few, stem trichomes. The presence of naked seeds in most Gb varieties was another characteristic that differed from the Gh varieties. Out of 121 Gb varieties, 61 (50%) had less fuzz fiber on seeds (fuzz fiber density less than 2) than the modern Gh varieties. An association analysis revealed very close correlation between the densities of stem trichomes and fuzz fibers (r = 0.501**, P < 0.05) (Table S4), suggesting that the genetic foundation of Gb stem trichome development was at least partially the same as that of fibers found in Gh.
Stem trichome development had simpler genetic control than leaf trichome
Trichomes, as part of the outermost layer of the plant body, are important for resistance to biotic and abiotic stresses. The molecular mechanisms of their growth, as a unique model, have been investigated extensively, including their morphology and botanical genesis, especially in Arabidopsis . Cotton trichomes have received even more attention than most, owing to similarity to seed trichomes (fibers, the primary economic product) in growth and evidence that these organs have an overlapping genetic basis. A classical genetic study indicated that cotton pubescence (mostly on leaf trichomes) was mainly controlled by five loci (t1–t5) . A corresponding allelic series was renamed T1, T1h, T1to,and T1an .T1 on Chr. 06 is the main locus for whole-plant pubescence, including stem trichomes [13, 14].
Genetic mapping using DNA markers allocated the loci for leaf pubescence onto five chromosomes. The major locus, recognized as t1, was mapped to the centromeric region of Chr. 06, and the other four (t2–t5) were mapped to chromosomes 01, 07, 23, and 25, respectively . Interestingly, only one locus for stem trichomes was detected, on Chr. 23. In another study , only the T1locus for leaf pubescence was again found in the same region of Chr. 06. Seven QTLs for leaf trichomes were mapped to different chromosomes: LGA01 (Chr. 13), Chr. 17, and LG. D03 (Chr. 24) . Only two QTLs for stem pubescence were mapped, to Chr. 06, the same as for leaf trichomes, and Chr. 24, respectively. Thus, three main loci for stem pubescence were identified, fewer than for leaf pubescence, and only T1 on Chr. 6 is also essential for leaf pubescence [16, 22, 25].
Many Gh varieties/wild species have glabrous stems, but pubescent leaves (Fig. 7). The glabrous stems of Gh varieties and sparse trichomes (Type III) of Gb varieties were confirmed here to be controlled by a dominant gene on Chr. 24, consistent with an earlier report . These results suggest that stem trichome initiation has a simpler genetic foundation than leaf pubescence, with one major locus shared with leaves, and additional factors. Different leaf parts (petiole, margin, vein, and others) can have different numbers of trichomes, that can be mapped as different trichome traits , making the research more complicated, but there were no such variations for stems. In addition, stem trichome density was closely correlated with fuzz fiber density. The results suggested that stem trichomes are a very good model for investigating genetic mechanisms that regulate fiber development.
The stem trichome development of two cultivated tetraploid cottons was governed by different gene/allele combinations and experienced different evolutionary fates during domestication
A clear difference between Gh and Gb was reported in the molecular mapping of trichome traits, especially for stem trichomes, although their mapping populations were derived from crosses between Gh and Gb varieties [15, 25]. In the present study, Gh and Gb stem trichome phenotypes were classified into four types. Gh varieties normally had Types I or II trichomes, while Gb had Types III or IV trichomes. The F1 plants generated by crossing varieties having the same type of stem trichomes always showed a similar trichome phenotype, and those from varieties having different types of stem trichomes showed various stem trichome phenotypes, suggesting that the different types of stem trichomes are controlled by different genes or allele combinations. Gb varieties with glabrous stems and Type III trichomes were similar in phenotype, because they have no and few clustered trichomes, respectively. The glabrous stems were confirmed to result from a transposable element (TE) insertion in HD1, a candidate gene of T1, while this gene in cotton having Type III stem trichomes does not have such an insertion (Ding et al. 2015). This phenotype was confirmed to be caused by the gene on Chr. 24 in this study. The Gb parent Pima-S7 used by Wright et al. (1999) was confirmed to carry a TE insertion in HD1, while Gb variety VH8–4602 used by Lacape and Nguyen (2005) was inferred as having Type III trichomes, because several trichomes (0.33) appeared on the stems. These findings not only explain why different studies produced different mapping results for genes related to stem and leaf trichomes, but also support a previous conclusion  that similar genetic and molecular mechanisms regulate stem trichome initiation in both Gh and Gb. However, they have undergone significant levels of differentiation during their speciation.
Through genetic mapping using different cross combinations, Type I trichomes were found to be controlled by genes on Chr. 06 and Chr. 24, Type II by a gene on Chr. 06, and Types III and IV by a gene on Chr. 24. The allele on Chr. 06 of Type II is dominant to the corresponding Type I allele. In Gb, the allele on Chr. 24 for Type III was dominant to the allele for Type IV. Classic genetic mapping [15, 25] and a transgenic study , together with our current findings, indicate that T1 is a major locus involved in determining cotton stem trichome growth. Lacape and Nguyen (2005) first reported that the gene on Chr. 24 was probably another major locus for stem trichomes. The current study revealed that most glabrous stems of Gh wild accessions/cultivars and Type III stem trichomes of Gb varieties were controlled by a dominant gene on Chr. 24. Therefore, the genes on Chr. 06 and Chr. 24 are essential for determining the stem trichome phenotypes of the two tetraploid species. However, in the effort of mapping Gh Type I stem trichome, the genes on Chr.06 and Chr.24 only explain about 50% of phenotype variation, suggesting additional other genes, such as the one on Chr. 23 , exist regulating stem trichome development, and more efforts are required to fully understand their genetic mechanisms.
The whole-genome sequencing of the two cultivated tetraploid species revealed their genome differentiation during domestication and variety improvement at the DNA level, reflected by significant variations in plant morphology and fiber quality . In our previous studies, we indicated that the two species differ greatly in the proportions of varieties with and without stem trichomes among primitive accessions and modern cultivars . The glabrous stems of Gb are the result of TE insertions in the gene HD1, while Gh has other important genes in addition to HD1, probably including the one on Chr. 24, which cause glabrous stems. In our ongoing project, we found that the glabrous stems of most Gh wild accessions were caused by a SNP mutation in the promoter of the candidate gene (unpublished data). In addition, Gh wild accessions have more diverse kinds of stem trichome phenotypes than modern varieties. For example, more wild Gh accessions are glabrous, or have shorter and denser stem trichomes, compared with modern cultivars. Interestingly, these stem trichome phenotypes are closely correlated with naked seeds and short fiber length. Similarly, more diverse stem trichome types exist in the Gb wild accessions than in the modern varieties . This information, coupled with our knowledge of the key genes regulating stem trichome growth on Chrs. 06 and 24, suggests a hypothesis for the evolution of Gh and Gb stem trichomes along with fibers. According to this hypothesis, the glabrous stems of Gb wild accessions were caused by the TE insertion in HD1 on Chr. 06, while the glabrous stems of Gh wild accessions were mainly caused by gaining the function of the gene on Chr. 24 (unpublished data), except for a few also caused by TE insertions in HD1 . The close correlation between stem trichomes and fuzz fibers suggests that the former in modern varieties evolved after selection for fiber length. Thus, both trichomes and fibers evolved in parallel, and the current stem trichome phenotypes in modern tetraploid cottons are partly a result of selection for seed hairs during domestication and variety improvement.
Stem trichomes and seed fibers are epidermal hairs that are regulated by similar genetic factors
The trichomes of A. thaliana and cotton fibers are single-celled structures of epidermal organs. Thus, Arabidopsis could serve as a model for elucidating the genetic mechanisms controlling cotton fiber development [31, 32]. Many genes were identified by homoeologous cloning and confirmed to be related to fiber development . There has been long-standing interest in whether the genetics of simply inherited traits, such as trichomes in cotton, could increase our understanding of more complex processes, such as lint fiber development [31, 33]. Simpson (1947)  reported that the pilose (T1) trait, which results in short dense trichomes on the vegetative parts of upland cotton, was associated with short coarse fibers. Since then, pilose has been shown to be related to yield components and fiber quality [13, 14, 16, 29]. Later, the pilose (T1) trait was confirmed to be controlled by HD1 on Chr. 06 .
While the present study and several others focus on genotypic correlations between stem trichomes and seed fibers associated with variation on chromosomes 6 and 24, appreciable evidence suggests that this correlation applies to additional genes across the genome. In the current study, the growth of Gh stem trichomes was very closely correlated with fuzz fibers in both wild accessions and fiber mutants. The Gb stem trichome density was closely correlated with fuzz fiber density. These findings supplement and complement an independent study in which106 lines with leaf and stem trichome variations were shown to often have altered lint fiber characteristics, supporting the hypothesis that there is considerable overlap in the sets of genetic factors acting in the development of these analogous organs . Revealing general mechanisms and specific genes regulating the density of stem trichomes will lay a foundation for understanding the mechanisms regulating the density of cotton fibers. In addition, our work can provide the cotton breeders with an idea that they should consider stem trichome as useful phenotype index during their selection of progenies in conventional breeding.
However, there are some limitations in this research which need more attentions in the future studies. (1) Not enough G. raimondii plants were used in morphology observation, which will probably affect the correct judgment of real stem trichome phenotype G. raimondii is a perennial species growing in the tropical areas of low latitudes and only five plants were keptin the green house. After observation, we found that they are all healthy and show consistent stem trichome phenotype, suggesting that they can be used as the representatives of G. raimondii plants. More G. raimondii plants should be included in the future for further trichome investigation and comparison between two diploid ancestors.(2) Limited plant numbers were used in F2 populations of (Liao1779x Xinyan96–48) and (Aken4154 xBazhou03), being 66 and 64 plants respectively (Table S5), which can only provide rough stem trichome genotype/phenotype correlation of Type I vs Type II and Type III vs Type IV cottons. In the future work, large mapping populations could be developed to uncover the close genetic relationship between different types of stem trichome. (3) Not enough DNA markers were used to cover entire genome in mapping QTL/genes related to stem trichome development. As a result, it may miss the discovery of other important genes as discussed in the previous section. Additional work should be considered to discover all possible stem trichome QTL/genes. Once more newly important trichome development related genes were mapped and cloned, its molecular regulating network will be further clearly revealed.
In this study, stem trichome phenotype of tetraploid cottons was classified into four types (I-IV) after systematical observation. Upland cotton normally have single (Type I) or single plus cluster (Type II) stem trichome, while Sea Island cotton have very short cluster trichome, and some have sparse (III) and other have very dense trichome (IV). Based on our findings together with other reports, stem trichome initiation is convinced to be controlled by simpler genetic foundation compared to leaf, mainly by the gene on Chr.06 and the one on Chr.24. Different types of stem trichome were mainly determined by combination of these genes/alleles. We also observed very close correlation between fuzzy fiber number and stem trichome density in both Gh and Gb primitive accessions and modern varieties. Based on above findings, we suggested that stem trichome evolved with seed fiber in parallel during domestication of cultivated tetraploid cottons.
Gossypium genotypes used for studying stem trichome density included 295 cultivated varieties, 180 wild accessions, and 37 fiber mutants of Gh; and 246 cultivated varieties of Gb (Table S1–4). All cotton materials were obtained from National Medium-term Gene Bank of Cotton in China. Gh wild accessions, Gh fiber mutants, and Gb cultivated varieties were also used for examining fuzz fiber density. The varieties used to produce the F1 hybrids, which were used to confirm the classifications of stem trichome types, and the F2 populations, which were used for mapping stem-trichome-related QTLs, are listed in Table S5. Gb varieties were planted in Shihezi, Xinjiang for trichome and fuzz fiber phenotype observation. Gh fiber mutants, Gh and Gb parents, and the F1 and F2 populations were planted in a farm at Zhejiang A&F University, Zhejiang Province, China. Gh varieties and wild races were planted in the National Wild Cotton Nursery, Sanya, China for fiber phenotype observation.
Observation of trichome and fuzz fiber phenotypes
The observation and density grading of stem trichomes were carried out as described . During the blooming period, the trichome phenotypes of the top and second internodes were visually observed twice by two different researchers in the field to determine the possible grades (Fig.S1). The internodes were cut and photographed using a KoPa® Microscope (M101) for further observation in the laboratory, and pictures of internodes with typical phenotypes were taken using a stereo microscope (OLYMPUS SZX10). Trichome phenotypes were classified into six grades (0–5) from the absence of trichomes to pilose based on trichome density (Fig.S2). The bolls on the middle fruit branches of the plants were harvested, and seeds were grouped into five types (0–4) based on the fuzz fiber numbers (Fig. S3). The association between phenotype and genotype was analyzed using correlation coefficients calculated by CORREL in Microsoft EXCEL at P < 0.05 according to the t-tests.
Total genomic DNA was extracted from young leaves of different genotypes, including varieties, parents and each F2 individual, using a modified CTAB method . According to a G. raimondii genome sequence  and tetraploid cotton TM-1 genome sequence , two types of molecular markers, simple sequence repeats (SSRs) and single-strand conformation polymorphisms (SSCPs) (Table S6), were developed to map trichome-related genes and QTLs. Primers were developed using Primer Premier (http://www.premierbiosoft.com/primerdesign/) and synthesized by BGI (Shanghai, China). PCR of SSR and SSCP markers were performed in 15-μL reaction mixtures each containing 1 μL of genomic DNA (100 ng/μL) as template, 0.3 μL of each primer (10 mmoL/L), 0.15 μL of rTaq DNA polymerase (5 U/μL) (TaKaRa, Japan), 0.25 μL of dNTPs (10 mmoL/L), and 1.5 μL of buffer solution (10×). The reaction program consisted of one cycle at 94 °C for 5 min, followed by 30 cycles at 94 °C for 30 s, 55 °C (according to the Tm values of different primers) for 40 s, and 72 °C for 30 s, followed by a final extension at 72 °C for 10 min. The PCR products were separated on a 1.0% polyacrylamide gel in 1× TBE buffer. After electrophoresis, the gel was silver stained. Analysis of SSCPs was carried out according to a procedure reported previously .
Map construction and QTL localization
All markers polymorphic between parents were initially used to survey the F2 populations for mapping of genes and QTLs associated with stem trichomes. Linkage analysis was carried out using JoinMap 4.0 and a LOD score of 3.0. The Kosambi map function  was used to convert recombination frequencies into map distances. QTLs were analyzed using the composite interval mapping function in the QTL Ici Mapping V3.3 software .
Availability of data and materials
All data generated or analyzed during this study are included in this published article [seethe supplementary information files].
- Gh :
- Gb :
Simple sequence repeats
Single-strand conformation polymorphism
- HD1 :
Homeodomain-leucine zipper gene
Guan XY, Yu N, Shangguan XX, Wang S, Lu S, Wang LJ, Chen XY. Arabidopsis trichome research sheds light on cotton fiber development mechanisms. Chin Sci Bull. 2007;52:1734–41.
Wang Z, Yang Z, Li F. Updates on molecular mechanisms in the development of branched trichome in Arabidopsis and nonbranched in cotton. Plant Biotechnol J. 2019;17:1706–22.
Payne T, Clement J, Arnold D, Lloyd A. Heterologous myb genes distinct from.GL1 enhance trichome production when overexpressed in Nicotiana tabacum. Development. 1999;126:671–82.
Larkin JC, Brown ML, Schiefelbein J. How do cells know what they want to be when they grow up? Lessons from epidermal patterning in Arabidopsis. Annu Rev Plant Biol. 2003;54:403–30.
Hülskamp M. Plant trichomes: a model for cell differentiation. Nat Rev Mol Cell Biol. 2004;5:471–80.
Szymanski DB, Lloyd AM, Marks MD. Progress in the molecular genetic analysis of trichome initiation and morphogenesis in Arabidopsis. Trends Plant Sci. 2000;5:214–9.
Morohashi K, Grotewold E. A systems approach reveals regulatory circuitry for Arabidopsis trichome initiation by the GL3 and GL1 selectors. PLoS Genet. 2009;5:1–17.
Bloomer RH, Juenger TE, Symonds VV. Natural variation in GL1 and its effects on trichome density in Arabidopsis thaliana. Mol Ecol. 2012;21:3501–15.
Lee MM, Schiefelbein J. WEREWOLF, a MYB-related protein in Arabidopsis, is a position-dependent regulator of epidermal cell patterning. Cell. 1999;99:473–83.
Zhao G, Wang S, Jia Y, Sun J. Genes related to fuzz initiation and development in Gossypium arboreum identified by cDNA microarray. Sci Agric Sin. 2010;13:430–7.
Yang C, Ye Z. Trichomes as models for studying plant cell differentiation. Cell Mol Life Sci. 2013;70:1937–48.
Qin YM, Zhu YX. How cotton fibers elongate: a tale of linear cell-growth mode. Curr Opin Plant Biol. 2011;14:106–11.
Kloth RH. New evidence relating the pilose allele and micronaire reading in cotton. Crop Sci. 1993;33:683–7.
Kloth RH. Quantitative trait loci affecting cotton fiber are linked to the T1 locus in upland cotton. Theor Appl Genet. 1995;91:762–8.
Wright RJ, Thaxton PM, El-Zik KM, Paterson AH. Molecular mapping of genes affecting pubescence of cotton. J Hered. 1999;90:215–9.
Wan Q, Zhang ZS, Hu MC, Chen L, Liu DJ, Chen X, Wang W, Zheng J. T1 locus in cotton is the candidate gene affecting lint percentage, fiber quality and spiny bollworm (Earias spp.) resistance. Euphytica. 2007;158:241–7.
Desai A, Chee PW, May OL, Paterson AH. Correspondence of trichome mutations in diploid and tetraploid cottons. J Hered. 2008;99:182–6.
He R, Zheng Y, Chen A, Ding M, Lin L, Cao Y, Zhou W, Rong J. Converting restriction fragment length polymorphism to single-strand conformation polymorphism markers and its application in the fine mapping of a trichome gene in cotton. Plant Breed. 2013;132:337–43.
Grover CE, Gallagher JP, Jareczek JJ, Page JT, Udall JA, Gore MA, Wendel JF. Re-evaluating the phylogeny of allopolyploid Gossypium L. Mol Phylogenet Evol. 2015;92:45–52.
Hu Y, Chen J, Fang L, Zhang Z, Ma W, Niu Y, Ju L, Deng J, Zhao T, Lian J, et al. Gossypium barbadense and Gossypium hirsutum genomes provide insights into the origin and evolution of allotetraploid cotton. Nat Genet. 2019;51:739–48.
Walford SA, Wu Y, Llewellyn DJ, Dennis ES. Dennis, epidermal cell differentiation in cotton mediated by the homeodomain leucine zipper gene, GhHD-1. Plant J. 2012;71:464–78.
Ding M, Ye W, Lin L, He S, Du X, Chen A, Cao Y, Qin Y, Yang F, Jiang Y, Zhang H, Wang X, Paterson AH, Rong J. The hairless stem phenotype of cotton (Gossypium barbadense) is linked to a copia-like retrotransposon insertion in a homeodomain-leucine zipper gene (HD1). Genetics. 2015;201:143–54.
Turley RB, Vaughn KC. Differential expression of trichomes on the leaves of upland cotton (Gossypium hirsutumL). J Cotton Sci. 2012;16:53–71.
Campbell BT, Saha S, Percy R, Frelichowski J, Jenkins J, Park W, Mayee C, Gotmare V, Dessauw D, Giband M, et al. Status of the global cotton germplasm resources. Crop Sci. 2010;50:1161–79.
Lacape JM, Nguyen TB. Mapping quantitative trait loci associated with leaf and stem pubescence in cotton. J Hered. 2005;96:441–4.
Tang M, Wu X, Cao Y, Qin Y, Ding M, Jiang Y, Sun C, Zhang H, Paterson AH, Rong J. Preferential insertion of a Ty1 LTR-retrotransposon into the a subgenome’s HD1 gene significantly correlated with the reduction in stem trichomes of tetraploid cotton. Mol Gen Genomics. 2019;295:47–54.
Zhang T, Hu Y, Jiang W, Fang L, Guan X, Chen J, Zhang J, Saski CA, Scheffler BE, Stelly DM, et al. Sequencing of allotetraploid cotton (Gossypium hirsutum L. acc. TM-1) provides a resource for fiber improvement. Nat Biotechnol. 2015;33:531–7.
Pesch M, Dartan B, Birkenbihl R, Somssich IE, Hülskamp M. Arabidopsis TTG2 regulates TRY expression through enhancement of activator complex-triggered activation. Plant Cell. 2014;26:4067–83.
Lee JA. Revision of the genetics of the hairiness-smoothness system of Gossypium. J Hered. 1985;76:123–6.
Lee JA. Genetics of the smooth stem character in Gossypium hirsutumL.1. Crop Sci. 1966;6:497–8.
Wang K, Wang Z, Li F, Ye W, Wang J, Song G, Yue Z, Cong L, Shang H, Zhu S, et al. The draft genome of a diploid cotton Gossypium raimondii. Nat Genet. 2012;44:1098–103.
Serna L, Martin C. Trichomes: different regulatory networks lead to convergent structures. Trends Plant Sci. 2006;11:274–80.
Patel JD, Wright RJ, Chandnani R, Goff VH, Ingles J, Paterson AH. EMS-mutated cotton populations suggest overlapping genetic control of trichome and lint fiber variation. Euphytica. 2016;208:597–608.
Simpson DM. Fuzzy leaf in cotton and its association with short lint. J Hered. 1947;38:153–6.
Zhang ZS, Hu MC, Zhang J, Liu DJ, Zheng J, Zhang K, Wang W, Wan Q. Construction of a comprehensive PCR-based marker linkage map and QTL mapping for fiber quality traits in upland cotton (Gossypium hirsutum L.). Mol Breed. 2009;24:49–61.
Paterson AH, Wendel JF, Gundlach H, Guo H, Jenkins J, Jin D, Llewellyn D, Showmaker KC, Shu S, Udall J, et al. Repeated polyploidization of Gossypium genomes and the evolution of spinnable cotton fibres. Nature. 2012;492:423–7.
Kosambi DD. The geometric method in mathematical statistics. Am Math Mon. 1944;7:382–9.
Zhang L, Wang S, Li H, Deng Q, Zheng A, Li S, Li P, Li Z, Wang J. Effect of missing marker and segregation distortion on QTL mapping in F2 populations. Theor Appl Genet. 2010;121:1071–82.
We are thankful to Professor Hongjie Li at The National Engineering Laboratory of Crop Molecular Breeding, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, China for his constructive suggestion and revision of the manuscript.
This work was supported by the National Key R & D Program for Crop Breeding (Grant no. 2016YFD0101417) to JR and the National Natural Science Foundation of China to YC (Grant no. 31501349) and YJ (Grant no. 31301372). The funders were not involved in the experimental design of the study, data collection, analysis and interpretation, and in writing the manuscript.
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Supplementary Figs. S1 to S5 (Fig. S1. Observations of cotton stem trichome phenotypes; Fig. S2. Stem trichome grading; Fig. S3. Seeds having different fuzzy fiber density levels grouped into five grades from 0 to 4 (from left to right); Fig. S4. Stem trichome phenotypes of the G. hirsutum wild accessions showing the different lengths and density levels; Fig. S5. Stem trichome phenotypes of parents and their F1 hybrids from crosses between G. hirsutum and G. babradense varieties with different types of trichomes.
Cultivated varieties of G. hirsutum used in this research. Table S2. G.hirsutum wild accessions used for observation of stem trichome density and fuzzy fiber. Table S3. Fussy fiber mutants of G. hirsutum used for observation of stem trichome density and fuzzy fiber. Table S4. Stem trichome and seed fiber of G. barbadense varieties. Table S5. Crosses used in mapping and classification of stem trichome type. Table S6. Stem trichome phenotype from NCGC. Table S7. G. arboreum stem trichome phenotypes. Table S8. Sequences, mapping location and physical position of SSR and SSCP primer used in mapping stem trichome. Table S9. Population derived from cross between Xinyan96–48 and Liao1779 for mapping Type II stem trichome. Table S10. Stem trichome phenotype of (Aken4154 x Bazhou03)F2 plants and their genotypes detected by D08–98. Table S11. Stem trichome phenotype of (QF-10/1 x Tu75–37) F2 plants and their genotypes detected by DNA markers, which were used for mapping Type I trichome of G. hirsutum. Table S12. Stem trichome phenotype of (N73DeltapineNGO x VIR-59TV)F2 plants and their genotypes detected by DNA markers, which were used for mapping Type III trichome of G. barbadense. Table S13. Stem trichome phenotype of (N73DeltapineNGO x Bazhou03)F2 plants and their genotypes detected by DNA markers, which were used for mapping Type IV trichome of G. barbadense.
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Yuan, R., Cao, Y., Li, T. et al. Differentiation in the genetic basis of stem trichome development between cultivated tetraploid cotton species. BMC Plant Biol 21, 115 (2021). https://doi.org/10.1186/s12870-021-02871-4
- Stem trichome
- Seed fiber
- Genetic mapping
- Correlation analysis
- Parallel evolution