Open Access

Molecular characterization of vernalization and response genes in bread wheat from the Yellow and Huai Valley of China

Contributed equally
BMC Plant Biology201313:199

https://doi.org/10.1186/1471-2229-13-199

Received: 20 June 2013

Accepted: 26 November 2013

Published: 5 December 2013

Abstract

Background

Flowering time greatly influences the adaptation of wheat cultivars to diverse environmental conditions and is mainly controlled by vernalization and photoperiod genes. In wheat cultivars from the Yellow and Huai Valleys, which represent 60%-70% of the total wheat production in China, the large-scale genotyping of wheat germplasms has not yet been performed in terms of vernalization and photoperiod response alleles, limiting the use of Chinese wheat germplasms to a certain extent.

Results

In this study, 173 winter wheat cultivars and 51 spring wheat cultivars from China were used to identify allelic variations of vernalization and photoperiod genes as well as copy number variations of Ppd-B1 and Vrn-A1. Two new co-dominant markers were developed in order to more precisely examine Vrn-A1b, Vrn-B1a, and Vrn-B1b. Two novel alleles at the Vrn-B3 locus were discovered and were designated Vrn-B3b and Vrn-B3c. Vrn-B3b had an 890-bp insertion in the promoter region of the recessive vrn-B3 allele, and Vrn-B3c allele had 2 deletions (a 20-bp deletion and a 4-bp deletion) in the promoter region of the dominant Vrn-B3a allele. Cultivar Hemai 26 lacked the Vrn-A1 gene. RT-PCR indicated that the 890-bp insertion in the Vrn-B3b allele significantly reduced the transcription of the Vrn-B3 gene. Cultivars Chadianhong with the Vrn-B3b allele and Hemai 26 with a Vrn-A1-null allele possessed relatively later heading and flowering times compared to those of Yanzhan 4110, which harbored recessive vrn-B3 and vrn-A1 alleles. Through identification of photoperiod genes, 2 new polymorphism combinations were found in 6 winter wheat cultivars and were designated Hapl-VII and Hapl-VIII, respectively. Distribution of the vernalization and photoperiod genes indicated that all recessive alleles at the 4 vernalization response loci, truncated “Chinese Spring” Ppd-B1 allele at Ppd-B1 locus and Hapl-I at the Ppd-D1 locus were predominant in Chinese winter wheat cultivars.

Conclusion

This study illustrated the distribution of vernalization and photoperiod genes and identified 2 new Vrn-B3 alleles, 1 Vrn-A1-null allele, and two new Ppd-D1 polymorphism combinations, using developed functional markers. Results of this study have the potential to provide useful information for screening relatively superior wheat cultivars for better adaptability and maturity.

Keywords

Bread wheat Vernalization response genes Photoperiod gene Flowering days Heading days

Background

The grain yield of wheat is determined not only by the genes directly controlling yield and yield components, but also by the genes controlling plant development and maturity [1]. Vernalization and photoperiod responses, which determine flowering and heading times, have a significant influence on the adaptability of wheat plants to a set of environmental conditions. The vernalization requirement of winter wheat cultivars (a prolonged exposure to low temperatures to accelerate flowering) protects the sensitive floral meristems from frost damage by cold temperatures. Differences in photoperiod sensitivity are also widely used in wheat breeding to provide adaptation to diverse agronomic environments.

Major vernalization response (Vrn) loci, which determine flowering and maturity times, have been mapped to the middle of the long arms of chromosomes 5 [25]. Moreover, vernalization response is actually controlled by 3 distinct Vrn loci in bread wheat. Vrn-1 genes, directly influencing flowering and maturity times, are located on chromosomes 5AL, 5BL and 5DL [6, 7] and were the first vernalization genes cloned in polyploid wheat by map-based cloning techniques [8]. Subsequently, Vrn-2 and Vrn-3 genes were cloned in wheat and barley by map-based cloning [9, 10]. However, Vrn-2 affected wheat growth habit as an indirect repressor of expression level of Vrn-A1 by repressing Vrn-3[11]. Loss-of-function Vrn-2 natural mutations or deletions result in the spring growth of bread wheat, which does not require vernalization to flower. The Vrn-3 gene, a homolog of the Arabidopsis FT gene [10, 12], exhibits increased expression if its dominant allele is present, resulting in accelerated flowering and a bypass of the vernalization requirement [10]. Therefore, the growth habits and vernalization requirements of cereal plants are mainly determined by 3 genes Vrn-1, Vrn-2 and Vrn-3.

Photoperiod response is another important factor that influences the flowering and maturity of wheat plants. Photoperiod insensitivity is widespread in bread wheat production areas globally and is particularly prevalent in regions where the crop is grown during short days or where crop maturity is required before the onset of high summer temperatures [13]. Based on several previous reports [1416], photoperiod response in bread wheat is mainly controlled by the Ppd-1 loci on the short arms of chromosomes 2D, 2B, and 2A. The Ppd-D1 allele for photoperiod insensitivity is generally considered the most potent, followed by Ppd-B1 and Ppd-A1[17, 18], though this view is still controversial due to conflicting results showing that Ppd-B1a could be as strong as Ppd-D1[19].

However, in the same type of wheat cultivars with winter or spring growth habits, there were still several-day differences among heading and flowering times. This difference mainly resulted from allelic variation in vernalization and photoperiod response genes at one or more loci. Therefore, identification of the vernalization and photoperiod response alleles will enhance the selection of cultivars with wide adaptability to a set of environments. Several vernalization and photoperiod response alleles have been identified in polyploidy wheat cultivars from different countries, subsequently leading to the development of a series of molecular markers for improved efficiency in identifying different vernalization and photoperiod response alleles [9, 15, 2023]. Fu et al. [20] indicated that the Argentine and Californian spring wheat cultivars showed a lower frequency of the dominant Vrn-A1 allele and a higher frequency of the dominant Vrn-D1 allele relative to the worldwide collection, though the dominant Vrn-A1 allele was the most popular genotype at the Vrn-A1 locus. Iqbal et al. [21] developed new molecular marker for identifying Vrn-A1 alleles and found that the dominant Vrn-A1a allele was the most prevalent while the dominant Vrn-D1 allele was absent in the Canadian spring wheat surveyed. Zhang et al. [24] found that the dominant Vrn-D1 allele showed the highest frequency in Chinese popular wheat cultivars (37.8%), followed by the dominant Vrn-A1, Vrn-B1, and Vrn-B3 alleles. They also showed that the Vrn-D1 allele is associated with the latest heading time, while Vrn-A1 is associated with the earliest heading time and Vrn-B1 is associated with an intermediate heading time. Santra et al. [22] and Shcherban et al. [25] identified 2 new Vrn-B1 alleles and found that a majority of the wheat germplasm surveyed carried the dominant allele Vrn-A1a alone or in combination with Vrn-B1, Vrn-D1, or Vrn-B3 alleles and that Vrn-B1 and Vrn-D1 alleles were almost always associated with other dominant Vrn-1 allele(s). Golovnina et al. [26] characterized great nucleotide variability in the region from -62 to -221 of the Vrn-1 promoter region in wild and cultivated wheats. Beales et al. [15] and Guo et al. [23] recently identified several polymorphisms in Ppd-D1 and Ppd-A1 loci of bread wheat.

Bread wheat (Triticum aestivum L.) is one of the 3 most important food crops in China, with more than 100 million tons produced annually in recent years. As a secondary origin center for bread wheat with a broad diversity of the germplasm, China is the largest producer and consumer of wheat in the world, and Chinese wheat germplasms differ from those of other countries in several aspects. Chinese wheat is mainly planted in 10 agro-ecological zones that are further divided into 26 sub-zones, with winter, facultative, and spring wheats sown both in autumn and spring [27]. Winter wheat occupies more than 85% of the total area and production of Chinese wheat. Of all agro-ecological zones, the Yellow and Huai wheat production region, covering all of Henan and parts of Shandong, Hebei, Shanxi, Shaanxi, Anhui and Jiangsu Provinces, is the most important and largest wheat production zone with 60%-70% of both total harvested area and total wheat production. In terms of requirements of temperature and days for vernalization, winter wheat cultivars from the Yellow and Huai Valley could be further divided into springness, semiwinterness and winterness wheat cultivars and are early in maturing in order to suit the double cropping system.

In this study we identified the distribution of vernalization and photoperiod response genes in winter wheat cultivars from the Yellow and Huai Valley, especially for landrace and current popular cultivars. In 2 landrace cultivars with winter growth habits, we found 2 novel Vrn-B3 alleles, 1 Vrn-A1-null allele and 2 new polymorphism combinations of photoperiod response alleles. These results provide useful information for the utilization of Chinese wheat germplasms in terms of growth habits.

Results

Discovery of 2 novel dominant Vrn-B3alleles in Chinese winter wheat

Screening of the 173 Chinese winter wheat cultivars by dominant PCR primer sets Vrn-P12F/R and Vrn-P13F/R (Table 1) indicated that 170 cultivars with the expected 1140-bp fragment size belonged to the recessive vrn-B3 allele. However, one Chinese landrace cultivar Chadianhong showed a fragment of approximately 2000 bp when amplified with primer set Vrn-P12F/R by 3 independent PCRs (Figure 1A), indicating that there was an approximately 900-bp insertion in Chadianhong in comparison with the recessive vrn-B3 allele. The approximately 2000-bp fragment was ligated into the pGEM-T Easy vector, and sequencing results of plasmids containing the targeted fragment indicated that an exact 890-bp fragment was inserted into the 5′ untranslated region (UTR) at -429 bp (reference to ATG; Figure 2A and Table 2). This new Vrn-3 allele was designated as Vrn-B3b (submitted to NCBI No: JN627519), according to the nomenclature of vernalization response genes by Fu et al. [20] and Yan et al. [9, 10].
Table 1

PCR primers for detecting vernalization response and Ppd-D1 alleles in bread wheat

Name

Allele or haplotype

Forward primer

Reverse primer

Expected band size (bp)

Annealing temp. °C

Reference

Vrn_P1

vrn-A1/Vrn-A1a/Vrn-A1b/Vrn-A1c

GAAAGGAAAAATTCTGCTCG

TGCACCTTCCC(C/G)CGCCCCAT

950 + 876 or 714 or 734

50

[9]

Vrn_P2

Vrn-A1b

CCTGCCGGAATCCTCGTTTT

CTACGCCCCTACCCTCCAACA

147 or 167

63

In this paper

Vrn-P3

Vrn-A1c

AGCCTCCACGGTTTGAAAGTAA

AAGTAAGACAACACGAATGTGAGA

1170

65

[20]

Vrn-P4

vrn-A1

GCACTCCTAACCCACTAACC

TCATCCATCATCAAGGCAAA

1068

59

[20]

Vrn-P5

Vrn-B1a

CAAGTGGAACGGTTAGGACA

CTCATGCCAAAAATTGAAGATGA

709

63

[20]

Vrn-P6

vrn-B1

CAAGTGGAACGGTTAGGACA

CAAATGAAAAGGAATGAGAGCA

1149

58

[20]

Vrn-P7

Vrn-B1b

CCAATCTCACATGCCTCCAA

ATGCGCCATGAACAACAAAG

215 or 252

59

In this paper

Vrn-P8

Vrn-D1a

GTTGTCTGCCTCATCAAATCC

GGTCACTGGTGGTCTGTGC

1671

63

[20]

Vrn-P9

vrn-D1

GTTGTCTGCCTCATCAAATCC

AAATGAAAAGGAACGGAGCG

997

59

[20]

Vrn-P10

Vrn-D1b

GTTGTCTGCCTCATCAAATCC

AGGATGGCCAGGCCAAAACG

612 bp

60

[28]

Vrn-P11

Vrn-D1b

GTTGTCTGCCTCATCAAATCC

AGGATGGCCAGGCCAAAACT

612 bp

60

[28]

Vrn-P12

vrn-B3

ATGCTTTCGCTTGCCATCC

CTATCCCTACCGGCCATTAG

1140 or 2030

56

[9]

Vrn-P13

Vrn-B3a

CATAATGCCAAGCCGGTGAGTAC

ATGTCTGCCAATTAGCTAGC

1200

59

[9]

Vrn-P14

Vrn-B3c

GCTTTGAACTCCAAGGAGAA

ATAATCAGCAGGTGAACCAG

1401

52

In this paper

Vrn-P15

vrn-B3/Vrn-B3

ACTCATCATCACCACTTCCT

TAATGCTTAATTCGTGGCTG

1499

51

In this paper

Vrn-P16

Vrn-B3 promoter

GTCCATACAAATCATGCCAC

TTCTGACAGTTTTAGTTGCG

491

51

In this paper

Vrn-P17

Vrn-B3 promoter

GCTTTCGCTTGCCATCCCAT

GCGGGAACGCTAATCTCCTG

898

62

In this paper

Vrn-P18

Vrn-B3 promoter

TTTGAGACAGGAGATTAGCG

ACCATCATGAGGCACCATTA

1131

53

In this paper

Vrn-P19

Vrn-B3 promoter

GCTTTGAACTCCAAGGAGAA

ATAATCAGCAGGTGAACCAG

1425

52

In this paper

Vrn-P20

Vrn-B3 promoter

CCGTTCACCATCTATTGCTC

CACCCAAATCCTTCATCTCA

1259

55

In this paper

Vrn-P21

CNV of Vrn-A1

CATTGTTCCTTCCTGTCCCACCC

ATTACTCGTACAGCCATCTCAGCC

1431

63

[29]

Vrn-B3-RT

-

GGAGGTGATGTGCTACGAGA

TTGTAGAGCTCGGCGAAGTC

147

55

In this paper

β-actin

-

GTTCCAATCTATGAGGGATACACGC

GAACCTCCACTGAGAACAACATTACC

422

56

[30]

Ppd-P1

Ppd-D1a

ACGCCTCCCACTACACTG

CACTGGTGGTAGCTGAGATT

288 or 2377

54

[15]

Ppd-P2

Ppd-D1b

ACGCCTCCCACTACACTG

GTTGGTTCAAACAGAGAGC

414 or 453

54

[15]

Ppd-P3

16 bp insertion Exon 8

GATGAACATGAAACGGG

GTCTAAATAGTAGGTACTAGG

320 or 336

52

[15]

Ppd-P4

TE deletion

AGGTCCTTACTCATACTCAATCTCA

CTCCCATTGTTGGTGTTGTTA

2612

50

[23]

Ppd-P5

2 kb deletion or TE insertion

CCATTCGAGGAGACGATTCAT

CTGAGAAAGAACAGAGTCAA

1005

55

[23]

Ppd-P6

5 bp deletion Exon 7

GAATGGCTTCTCCTGGTC

GATGGGCGAAACCTTATT

1,032 or 1,027

50

[23]

Ppd-P7

5 bp deletion Exon 7

GTGTCCTTTGCGAATCCTT

TTGGAGCCTTGCTTCATCT

184 or 179

53

[23]

Ppd-P8

Truncated Ppd-B1 gene in the ‘Chinese Spring’ allele

TAACTGCTCCTCACAAGTGC

CCGGAACCTGAGGATCATC

425

56

[31]

Ppd-P9

Intact Ppd-B1 copies in the ‘Chinese Spring’ allele

AAAACATTATGCATATAGCTTGTGTC

CAGACATGGACTCGGAACAC

994

58

[31]

Ppd-P10

Intact Ppd-B1 copies in the ‘Sonora64’/‘Timstein’ allele

CCAGGCGAGTGATTTACACA

GGGCACGTTAACACACCTTT

223

58

[31]

Figure 1

Identification of vernalization response alleles by newly developed co-dominant markers in Chinese wheat cultivars. A: Primer set Vrn-10 for identification of Vrn-B3c allele with 2030 bp. From left to right: Yunong 202, Yunong 201, Zhoumai 18, Chadianhong with three lanes, DNA ladder DL 2000. B: Primer set Vrn-2 for identification of Vrn-A1b allele with 147 bp. From left to right: DNA ladder DL 2000, Yumai 57, Aikang 58, Yunong 202, Jimai 38, Wuyimai, Huaimai 19, Bonong 5, Yumai 41, Yumai 51. C: Primer set Vrn-7 for identification of Vrn-B1b allele with 215 bp. From left to right: DNA ladder DL 2000, Gaoyuan 932, Gaoyuan 314, Gaoyuan 448, Gaoyuan 115, Qingchun 587, Qingchun 891, Qingchun 952, Gaoyuan 363, Gaoyuan 028, Gaoyuan 356, Gaoyuan 175, Gaoyuan 182, Gaoyuan 913, Humai 11, Humai 13, Humai 14, Humai 15, Minhe 588, Minhe 665, Lemai 5, Gaoyuan 602, Xinzhe 9, Qingchun 415, Qingchun 570.

Figure 2

Schematic representation of Vrn-B3 alleles identified in Chinese winter wheat cultivars. (A) P16-P18 are primers we designated in this study for identification of 5300-bp insertion in promoter sequence of Vrn-B3 gene) and Vrn-B1 (B) alleles identified in Chinese winter wheat.

Table 2

Names and the molecular characterization of vernalization response alleles currently reported in polyploid wheat

Locus

Allele

NCBI No.

Molecular characterization

Reference

Vrn-A1

vrn-A1

AY747600

-

[20]

 

Vrn-A1a

AY616458, AY616459

231-bp and 140-bp insertions at -439 bp and -348 bp, respectively.

[9]

 

Vrn-A1b

AY616461

20-bp deletion at -157 bp

[9]

 

Vrn-A1c

AY747599

5504-bp deletion at +1349 bp

[20]

 

Vrn-A1d

AY616462

32-bp deletion at -214 bp

[9]

 

Vrn-A1e

AY616463

54-bp deletion at -220 bp

[9]

Vrn-B1

vrn-B1

AY747604

-

[20]

 

Vrn-B1a

AY747603

6850-bp deletion at +836 bp

[20]

 

Vrn-B1b

FJ766015

6850-bp deletion at +836 bp and 37-bp deletion at +7992 bp

[22]

 

Vrn-B1c

HQ593668, HQ130482

817-bp deletion and 0.4-kb duplication at +798 bp

[32]

[25]

Vrn-B3

vrn-B3

DQ890162

-

[10]

 

Vrn-B3a

DQ890165

5300-bp insertion at -592 bp

[10]

 

Vrn-B3b

JN627519

890-bp insertion at -429 bp

In this paper

 

Vrn-B3c

JQ082311

5300-bp insertion at -592 bp but 20-bp and 4-bp deletions at -3543 bp and -3591 bp

In this paper

Vrn-D1

vrn-D1

AY747606

-

[20]

 

Vrn-D1a

AY747597

4235-bp deletion at +810 bp

[20]

When amplified with primer set Vrn-P12F/R (Table 1), we did not obtain any PCR product in the 2 winter cultivars Ji 874–109 and Hemai 26. Because primer set Vrn-P13F/R did not work very well in these2 cultivars, 5 primer sets (Vrn-P16 ~ Vrn-P20 in Table 1) were designed at the different positions of the Vrn-B3 locus based on the sequence of DQ890165. All PCR products amplified in cultivars Ji 874–109 and Hemai 26 were then sequenced from both directions. Results indicated that sequences amplified with 4 primer sets were identical to Vrn-B3a (data not listed), whereas the sequence amplified with primer set Vrn-P19F/R (Table 1) identified 2 deletions in landrace cultivar Ji 874–109: a 20-bp fragment at -3543 bp and a 4-bp fragment at -3591 bp in the 5′-UTR (Table 2), when compared with the Vrn-B3a allele. This new Vrn-B3 allele was designated Vrn-B3c allele (NCBI No: JQ082311) according to the nomenclature of Yan et al. [9], Fu et al. [20], and Shcherban et al. [25]. The cultivar Hemai 26 showed the same molecular characterization as that of Vrn-B3a.

Expression of different Vrn-B3alleles in winter wheat and their association with days to heading (DH) and days to flowering (DF)

Four cultivars, i.e., Ji 874–109 (Vrn-B3c), Yanzhan 4110 (vrn-B3), Chadianhong (Vrn-B3b), and Hemai 26 (Vrn-B3a), with different Vrn-B3 alleles were selected to compare expression levels by real-time PCR. Sequencing the Vrn-B3 coding region (amplification with primer set Vrn-P15 R/F in Table 1) of the 4 above-mentioned cultivars showed that they were 100% identical on the DNA level (data not shown). Real-time PCR (Figure 3) indicated the landrace cultivar Chadianhong with the Vrn-B3b allele possessed significantly lower expression level than Yanzhan 4110 with the recessive vrn-B3 allele, suggesting that the 890-bp insertion in Vrn-B3b allele possibly contributed to its reduced expression level. However, wheat accession Ji 874–109 with the Vrn-B3c allele did not show significant difference at the transcript level from Hemai 26 with the Vrn-B3a allele, even though the expression level of the Vrn-B3c allele was relatively lower than that of the Vrn-B3a allele. This suggested that the 2 deletions (20-bp and 4-bp) may not have had a significant effect on Vrn-B3a promoter activity. In addition, RT-PCR indicated that Hemai 26 possessed the highest expression at the transcript level of Vrn-B3 alleles among the 4 cultivars. Although the difference in Vrn-B3 expression between Hemai 26 and Ji 874–109 was not significant on the transcript level (Figure 3), these results suggested that the 5300-bp insertion in Vrn-B3a and Vrn-B3c alleles possibly contributeed to their increased transcription.
Figure 3

Comparison of relative expression levels of 4 varieties with different Vrn-B3 alleles by real-time PCR.

Currently, the Chinese cultivar Yanzhan 4110 is being used as a control for releasing new wheat cultivars in yield comparison trials of Winter Wheat Regional Field Testing of the Yellow and Huai Valley southern region. Under the vernalization conditions in the field and compared with Yanzhan 4110 (192 DH and 196 DF), wheat cultivar Chadianhong (202 DH and 207 DF) with the Vrn-B3b allele headed 10 days later and flowered 11 days later, and Hemai 26 (197 DH and 202 DF) with the Vrn-B3a allele headed 5 days later and flowered 6 days later. The cultivar Ji 874–109 (191 DH and 197 DF) with the Vrn-B3c allele, however, showed only ± 1 day differences in heading and flowering times from those of Yanzhan 4110 (see Additional file 1).

Moreover, the 4 above-mentioned cultivars without vernalization were further investigated for their heading and flowering days, in a greenhouse with 16 h daylight cycles, to test their vernalization requirements. Results indicated that 3 cultivars, i.e., Ji 874–109 (89 DH and 101 DF), Hemai 26 (138 DH and 149 DF), and Chadianhong (158 DH and 169 DF) headed 9, 58, and 78 days later and flowered 9, 57, and 77 days later, respectively, when compared with Yanzhan 4110 (80 DH and 92 DF).

Distribution of vernalization response and Ppd-D1alleles in Chinese winter wheat cultivars surveyed

Based on sequences of AY747600 and AY747601, we developed a new co-dominant marker Vrn-P2F/R (Table 1) for more precise identification of the Vrn-A1b allele (Figure 1B) by replacing the marker Vrn-P1F/R previously developed by Yan et al. [9]. Sequencing results showed reliability of the new marker Vrn-P2F/R. Using the allele-specific primer sets Vrn-P1F/R ~ Vrn-P4F/R, we showed that 161 out of 173 winter wheat cultivars possessed the recessive vrn-A1 allele at the Vrn-A1 locus. Nine of these possessed the Vrn-Ala allele, and 2 cultivars (Yumai 1 and Wuyimai) possessed the Vrn-Alb allele (Table 3). However, a cultivar (Hemai 26) from Henan did not show any PCR product when amplified with the above-mentioned 4 primer sets, possibly indicating that there was a large deletion at the Vrn-A1 locus of Hemai 26. Therefore, the above-mentioned later heading and flowering times of Hemai 26 may be primarily because of its Vrn-A1 deletion, even though the expression level of the Vrn-B3 allele in this cultivar was not significantly lower than that of Yanzhan 4110. Genotyping results suggested that the recessive allele vrn-A1 was predominant at the Vrn-A1 locus in winter wheat cultivars from the Yellow and Huai Valley of China. Of the 51 spring wheat we surveyed, 31, 18, and 2 had vrn-A, Vrn-A1a, and Vrn-V1b alleles, respectively (see Additional file 1).
Table 3

Distribution of known vernalization response alleles and Ppd-D1 haplotypes in bread wheat cultivars from the Yellow and Huai Valley of China

Locus

Allele/haplotype

Henan

Hebei

Shaanxi

Shandong

Shanxi

Others

Total

Sample No.

85

20

19

13

7

29

173

Vrn-A1

vrn-A1

79

20

19

13

7

23

161

 

Vrn-A1a

4

0

0

0

0

5

9

 

Vrn-A1b

1

0

0

0

0

1

2

Vrn-B1

vrn-B1

80

19

18

12

7

25

161

 

Vrn-B1a

5

1

1

1

0

4

12

Vrn-B3

vrn-B3

84

18

19

13

7

29

170

 

Vrn-B3a

1

0

0

0

0

0

1

 

Vrn-B3b

0

1

0

0

0

0

1

 

Vrn-B3c

0

1

0

0

0

0

1

Vrn-D1

vrn-D1

54

13

9

8

6

17

107

 

Vrn-D1a

13

2

3

2

 

4

24

 

Vrn-D1b

18

5

7

3

1

8

42

Ppd-D1

Hapl-I

84

15

19

12

6

19

155

 

Hapl-II

0

2

0

0

0

1

3

 

Hapl-III

0

0

0

0

0

1

1

 

Hapl-IV

1

0

0

1

1

5

8

 

Hapl-VII

0

2

0

0

0

2

4

 

Hapl-VIII

0

0

1

0

0

1

2

Two previously developed primer sets Vrn-P5F/R and Vrn-P6F/R were used to identify recessive and dominant alleles at the Vrn-B1 locus in Chinese winter wheat cultivars. In order to identify Vrn-B1a and Vrn-B1b alleles, recently reported by Santra et al. [22] and Milec et al. [32], we developed a new co-dominant marker Vrn-P7F/R (Table 1) with a 215-bp fragment for the Vrn-B1a allele and a 252-bp fragment for the Vrn-B1b allele (Figure 1C), based on the characterization of Vrn-B1 alleles (Figure 2B). Sequencing results confirmed its reliability. Due to the absence of the Vrn-B1b allele in the Chinese winter wheat cultivars surveyed in this study, we also collected 51 currently popular spring wheat cultivars from Gansu for detection of the Vrn-B1b allele, using the co-dominance of primer set Vrn-P7F/R (Figure 1C). Genotyping results using primer sets Vrn-P5F/R, Vrn-P6F/R, and Vrn-P7F/R (Table 1) indicated that 161 out of 173 winter wheat cultivars had the recessive vrn-B1 allele (accounting for 93.1%), while 12 cultivars had the Vrn-B1a allele (accounting for 6.9%; Table 3). This suggested that the recessive allele vrn-B1 was predominant at the Vrn-B1 locus in winter wheat cultivars from the Yellow and Huai Valley of China. Of the 51 spring wheat cultivars we surveyed, 13, 24, and 14 had vrn-B1, Vrn-B1a, and Vrn-B1b alleles, respectively (see Additional file 1).

Among the Chinese winter wheat cultivars we surveyed, 170 out of 173 cultivars had the recessive vrn-B3 allele, accounting for 98.3%; while only 1 cultivar (Hemai 26) was identified as having Vrn-B3a, 1 cultivar (Chadianhong) as having Vrn-B3b, and 1 cultivar (Ji 874–109) as having Vrn-B3c, as described above (Table 3). This suggested that the recessive vrn-B3 allele was the predominant genotype at the Vrn-B3 locus in winter wheat cultivars from the Yellow and Huai Valley of China. In the spring wheat we surveyed, all 51 cultivars have the same allele vrn-B3.

Genotyping results with primer sets Vrn-P8F/R and Vrn-P9F/R showed that 107 out of 173 winter wheat cultivars possessed the recessive vrn-D1 allele (accounting for 61.9%), and 66 cultivars possessed the dominant Vrn-D1 allele (Table 3). Further identification with markers Vrn-P10F/R and Vrn-11 F/R showed that 24 and 42 out of 66 cultivars had Vrn-D1a (accounting for 13.9%) and Vrn-D1b alleles (accounting for 24.2%), respectively. These data suggested that the dominant Vrn-D1a and Vrn-D1b alleles were prevalent in Chinese winter wheat cultivars even though the recessive vrn-D1 allele was still the predominant genotype at the Vrn-D1 locus in winter wheat cultivars from the Yellow and Huai Valley of China. A similar observation was described by Zhang et al. [24, 28]. Of the 51 spring wheat cultivars we surveyed, 32 and 19 had vrn-D1 and Vrn-D1a alleles, respectively (see Additional file 1).

Characterization of the allelic combination of vernalization response genes at Vrn-A1, Vrn-B1, Vrn-D1, and Vrn-B3 loci revealed that 92 out of the 173 Chinese winter wheat cultivars surveyed had vrn-A1/vrn-B1/vrn-D1/vrn-B3 (53.2%), 30 cultivars possessed vrn-A1/vrn-B1/Vrn-D1a/vrn-B3 (17.3%), 37 cultivars possessed vrn-A1/vrn-B1/Vrn-D1b/vrn-B3 (21.4%), 6 cultivars possessed vrn-A1/Vrn-B1a/vrn-D1/vrn-B3, 5 cultivars possessed Vrn-A1a/vrn-B1/vrn-D1/vrn-B3, 2 cultivars (Huixianhong and Fan 6) possessed vrn-A1/Vrn-B1a/Vrn-D1a/vrn-B3, 2 cultivars (Xibeiaigezi and Aimengniu) possessed vrn-A1/Vrn-B1a/Vrn-D1b/vrn-B3, 2 cultivars (Xichuan 76–9 and Zhenghua 3563) possessed Vrn-A1a/vrn-B1/Vrn-D1a/vrn-B3, 2 cultivars (Zhenghua 0840–3 and Xinkehan 9) possessed Vrn-A1a/vrn-B1/Vrn-D1b/vrn-B3, 1 cultivar (Ji 874–109) possessed vrn-A1/Vrn-B1a/vrn-D1/Vrn-B3c, 1 cultivar (Chadianhong) had vrn-A1/vrn-B1/Vrn-D1b/Vrn-B3b, 1 cultivar (Hemai 26) possessed vrn-B1/vrn-D1/Vrn-B3a (possible lack of the Vrn-A1 gene), 1 cultivar (Yumai 1) possessed Vrn-A1b/vrn-B1/vrn-D1/vrn-B3 and 1 cultivar Wuyimai possessed Vrn-A1b/Vrn-B1a/vrn-D1/vrn-B3. A total of 14 allelic combinations for vernalization response genes were discovered in the Chinese winter wheat surveyed. All these suggested that the recessive allelic combination of vrn-A1/vrn-B1/vrn-D1/vrn-B3 was predominant, but the combinations of vrn-A1/vrn-B1/Vrn-D1a/vrn-B3 and vrn-A1/vrn-B1/Vrn-D1b/vrn-B3 were prevalent in winter wheat cultivars from the Yellow and Huai Valley of China.

Distribution of the Ppd-D1gene in Chinese winter wheat cultivars

A series of molecular markers (Ppd-P1 ~ Ppd-P7, Table 1) were used to identify Ppd-D1 sequence polymorphisms according to the methods described by Guo et al. [23]. In total, 3 polymorphisms were found in bread wheat cultivars, i.e. a 2089-bp deletion in exon 8, the mariner-like transposable element (TE) insertion in intron 1, and a 5-bp deletion in exon 7; two polymorphisms were not found, i.e., a 16-bp insertion in exon 8 and a 24-bp plus a 15-bp insertions in the 2-kp upstream region.

In the 173 winter wheat cultivars surveyed in this study, 161 cultivars had a 2089-bp deletion upstream of the coding region and possessed the photoperiod-insensitive Ppd-D1a allele, which causes early flowering, whereas the remaining 12 cultivars had the photoperiod-sensitive Ppd-D1b allele, which causes later flowering. Moreover, 5 cultivars were identified as possessing the mariner-like TE in intron 1 of the Ppd-D1 gene, and 10 cultivars were identified as possessing 5-bp deletion in exon 7, which created a frame shift and resulted in a nonfunctional protein. All 173 cultivars possessed a 16-bp deletion containing the last 2 bases of the CCT domain in exon 8. However, no cultivar was found to have 24-bp plus 15-bp insertions in the 2-kb upstream region reported in synthetic wheats and A. tauschii accessions by Guo et al. [23].

Furthermore, 6 combinations of the 3 above-mentioned polymorphisms (Table 4) were examined in winter wheat cultivars from the Yellow and Huai Valley of China. However, there were 2 novel Ppd-D1 polymorphism combinations identified in this study when compared to those reported by Guo et al. [23], i.e., absence of 2089 bp in exon 8 and presence of both TE in intron 1 and 5 bp in exon 7 for 4 cultivars: Danmai 1 introduced from Danmark (213 DH and 217 DF), Ji 923235 (194 DH and 198 DF), Ji 874–109 (191 DH and 197 DF), and Huapeiai (191 DH and 197 DF), and absence of 2089 bp in exon 8, TE in intron 1, and 5 bp in exon 7 for 2 cultivars Damuzhiai (210 DH and 215 DF) and Xian 83(104)-11 Zhong “S” (202 DH and 208 DF). We designated them as Hapl-VII (absence of 2089 bp in exon 8 and presence of both TE in intron 1 and 5 bp in exon 7) and Hapl-VIII (absence of 2089 bp in exon 8, TE in intron 1 and 5 bp in exon 7) according to the nomenclature of Guo et al. [23]. Of 6 polymorphism combinations, Hapl-I was the most prevalent, found in 89.6% of Chinese winter wheat cultivars surveyed from the Yellow and Huai Valley of China (Table 3).
Table 4

Ppd-D1 haplotypes identified in bread wheat cultivars from the Yellow and Huai Valley of China

Ppd-D1Haplotype

Sample no.

24 bp plus 15 bp

2 kb

TE

5 bp

16 bp

I

155

-

-

-

+

-

II

3

-

+

-

+

-

III

1

-

+

+

+

-

IV

8

-

+

-

-

-

V

0

-

+

-

+

+

VI

0

+

+

-

+

+

VII

4

-

-

+

+

-

XIII

2

-

-

-

-

-

Insertions and deletions are indicated by + and -, respectively.

Copy number variations (CNVs) at the Ppd-B1 and Vrn-A1loci

CNV is a type of mutation that has been widely studied in human genetics; these studies have sharply increased in plants recently due to its possible influence on phenotype. Based on the report of Díaz et al. [31], the Ppd-B1a gene has 3 types in view of CNV, i.e., truncated ‘Chinese Spring’ Ppd-B1a allele, intact ‘Chinese Spring’ Ppd-B1a allele, and ‘Sonora64’ allele. Wheat plants with the ‘Sonora64’ Ppd-B1a allele have been shown to flower earlier than those with the ‘Chinese Spring’ Ppd-B1a allele [31]. Identification of the above 3 Ppd-B1a alleles by specific primers (Ppd-P8 ~ Ppd-P10, Table 1) indicated that 109, 42, and 51 wheat cultivars possessed the truncated ‘Chinese Spring’ Ppd-B1a, intact ‘Chinese Spring’ Ppd-B1a and ‘Sonora64’ alleles, respectively, in the surveyed winter wheat from the Yellow and Huai Valley of China (see Additional file 1). Interestingly, all 42 cultivars with the intact ‘Chinese Spring’ Ppd-B1a allele contained the truncated ‘Chinese Spring’ Ppd-B1a allele, and 27 out of 51 cultivars with the intact ‘Sonora64’ allele contained the truncated ‘Chinese Spring’ Ppd-B1a allele.

CNV of the Vrn-A1 gene were examined by the marker Pri_21F/R previously developed by Eagles et al. [29]. Because PCR products amplified by this marker contained more than one fragment and could not be directly sequenced even though we tried several times, 34 out of 173 winter wheat cultivars were selected to identify CNV of Vrn-A1 by sequencing sub-clones. Results indicated that 18 wheat cultivars possessed both C and T sequences in exon 4 and the other 16 remaining cultivars only possessed the C sequence in exon 4 of the Vrn-A1 gene (see Additional file 1).

Discussion

In the Yellow and Huai wheat production region of China, the grain-filling stage of winter wheat cultivars usually lasts approximate 40 days from late April to early June for almost every cropping seasons; this may fluctuate according to the environmental characteristics of specific regions or provinces. However, farmers generally would like to plant early-maturing wheat cultivars in their fields due to the frequent presence of dry-hot winds in early June or late May, especially in Henan, which is the most important wheat production province in view of the yield and area in China. Based on a number of studies [8, 15, 20, 31], vernalization and photoperiod response genes as well as their copy number variations have an important influence on plant flowering and maturity. In this study, we found that certain combinations of vernalization alleles and photoperiod haplotypes showed early-maturing characteristics, which would possibly provide useful information for screening early-maturing wheat cultivars by marker-assisted selection (MAS). For example, the winter wheat cultivars surveyed with the combination of vrn-A1/Vrn-B1b/Vrn-B3a/Vrn-D1a/Ppd-D1a headed and flowered an average of 3 days earlier than cultivars with the combination of vrn-A1/vrn-B1/Vrn-B3a/Vrn-D1a/Ppd-D1a. However, we did not exactly compare them due to the small number of cultivars with the exact same vernalization response and photoperiod alleles for certain combinations.

Since the vernalization response gene was cloned ten years ago [6, 8, 33, 34], a number of functional molecular markers, derived from polymorphic sites within genes that directly affect phenotypic trait variation, have been developed for identification of diverse vernalization response alleles in ployploid wheat [8, 9, 20, 22, 25, 32]. Also, several vernalization alleles have been identified in bread and durum wheat cultivars from different geographical environments. Even though some similar studies have been conducted in Chinese winter wheat cultivars from different agro-ecological zones, the large scale genotyping of wheat germplasms has still not been performed to provide details on vernalization and photoperiod response genes in winter wheat cultivars from the Yellow and Huai Valley of China, especially in landrace cultivars and more recent cultivars, because in this wheat region more than 50 new wheat cultivars are released every year, and more than 3000 landrace and historical cultivars are kept in different wheat germplasm banks. Therefore, further screening of the relatively superior genotypes of vernalization response and photoperiod genes would be beneficial for improving the adaptability of bread wheat.

Photoperiod response genes play an import role in wheat growth and development. Photoperiod insensitive cultivars flower under short-day and long-day conditions, whereas photoperiod-sensitive cultivars usually delay heading and flowering and may even not undergo heading if the day length and number of long days do not meet the minimum requirement of sensitive cultivars to head and flower. However, few studies have focused on identification of allelic variation of photoperiod genes in bread wheat and only 2 alleles have been found at each locus, i.e., photoperiod insensitive (Ppd-D1a and Ppd-B1a) and photoperiod sensitive (Ppd-D1b and Ppd-B1b). Moreover, 5 Ppd-D1 alleles were identified by Beales et al. [15], but only the 2 kb deletion was associated with photoperiod insensitivity. However, those five alleles were expressed as haplotypes by Guo et al. [23] due to the simultaneous presence of more than one polymorphism in the Ppd-D1 locus. Therefore, we suggest using the method of designating haplotypes to name the different combinations of diverse polymorphisms, instead of alleles, in describing photoperiod gene variations in the D genome of bread wheat cultivars. Based on our study, it seems that not only a 2-kb deletion, but also other polymorphisms have an impact on days to heading and flowering due to the obvious differences between Chinese cultivars with HapVII and Hap VIII. However, more work needs to be conducted to further support this conclusion.

Changes in the promoter sequence are quite common in the known vernalization response genes in bread wheat. Four of 5 Vrn-A1 alleles previously reported were resulted from mutations of the promoter sequence at the Vrn-A1 locus. In this study, 2 new alleles, Vrn-B3b and Vrn-B3c, were caused by changes in the promoter sequence at the Vrn-B3 locus. A 5300-bp insertion in the promoter region of Vrn-B3 has been shown to cause early flowering [10]. However, in this study, the new allele Vrn-B3b, having an 890-bp insertion significantly reduced the expression level of the gene and caused later heading and flowering. Our results also suggested that the special promoter sequence of Vrn-B3b may be useful to further analysis of promoter influence on the expression levels of genes.

A previous study indicated that overexpression of the Vrn-3 gene in winter wheat could result in up-regulation of the Vrn-1 gene and a spring growth habit [35]. We also found that the wheat cultivar with the Vrn-B3a allele possessed significantly higher expression at the transcript level, as shown by RT-PCR. Therefore, it is plausible that the Vrn-B3a allele in wheat cultivar Hope caused FT overexpression and early flowering [10]. However, in this study, the wheat cultivar Hemai 26 with the Vrn-B3a allele also exhibited deletion of Vrn-A1, and its later flowering was possibly caused by this Vrn-A1 deletion because the Vrn-A1 gene may have a greater impact on flowering time than the Vrn-B3 gene, even though Hemai 26 exhibited overexpression of Vrn-B3. However, Chadianhong, which possessed the Vrn-B3b allele, exhibited later flowering possibly because of its 890-bp insertion, which reduced expression of the Vrn-3 gene, instead of a 5300-bp insertion which would result in increased expression. Therefore, the later heading and flowering times of some cultivars surveyed in this study may have resulted from the relatively low expression of Vrn-B3, leading to the reduced expression of the Vrn-1 gene. However, due to the discovery of the Vrn-4 gene, there are still other unknown genes related to vernalization and photoperiod response in bread wheat, and the differences amongst days to heading and flowering of diverse cultivars should result from the combination of multiple determinants including vernalization, photoperiod response genes and their CNVs.

Conclusion

We characterized the allelic variations of vernalization and photoperiod response genes as well as their CNVs in 173 winter wheat and 51 spring wheat cultivars of China, found 2 new Vrn-B3 alleles, 1 new Vrn-A1 allele and 2 new polymorphism combinations at the photoperiod locus, and developed functional markers for identifying different vernalization response alleles. Cultivars with new Vrn-B1 or Vrn-A1 alleles headed and flowered significantly later under the condition of non-vernalization. This study could provide useful information for screening relatively superior wheat cultivars for better adaptability and maturity in Yellow and Huai Valley of China.

Methods

Plant materials

In this study, 173 winter wheat accessions composed of landrace cultivars and current popular cultivars from the Yellow and Huai Valley of China, mainly collected from Henan, Hebei, Shaanxi, Shanxi and Shandong, were planted in October, 2010 and harvested in the June, 2011 cropping season at the Zhengzhou Scientific Research and Education Center of Henan Agricultural University (longitude: 113.6; latitude: 34.9) under local management practices. The field experiment was performed using a completely random design. Each plot contained four 200 cm-long rows with 23 cm between neighboring rows and 10 cm between neighboring plants. All surveyed cultivars, vernalized through the winter with an average temperature of 1.3°C (December, January, and February) in 2011, grew very well with the supporting net and no lodging was present in the trial. DH and DF were investigated for each cultivar surveyed before harvesting.

In addition, 51 spring wheat cultivars, kindly provided by Liu Baolong from Northwest Institute of Plateau Biology of Chinese Academy of Sciences, were used to detect the vernalization response alleles at Vrn-A1, Vrn-B1 and Vrn-D1 loci.

PCR amplification

The genomic DNA of each cultivar surveyed was individually extracted from 3 pulverized kernels, following a method described by Chen et al. [36]. The PCR amplification reactions were conducted in a 25-μL reaction volume containing 100 ng genomic DNA, 10 pmol of each primer (Table 1), 200 μM of each dNTP, 1× Taq DNA polymerase reaction buffer with 1.5 μM MgCl2, and 0.5 unit of Taq DNA polymerase using PTC-200 Peltier Thermocycler or ABI 9700. The cycling conditions were as follows: 94°C for 5 min followed by 35 cycles of 94°C for 40 s, 50°C to 65°C for 40 s (primer-specific annealing temperatures, see Table 1), and 72°C for 1.5 min, followed by a final 10-min extension at 72°C. PCR products were separated by electrophoresis either on a 1.5% ~ 2.5% agarose gel stained with ethidium bromide and visualized using UV light, or on a 6% polyacrylamide gel and resolved by silver staining [37].

DNA sequencing

PCR products were purified using Quick DNA Extraction Kit (Takara, Otsu, Japan), ligated into the pGEM-T Easy vector, and transformed into competent cells of the Escherichia coli DH-5α strain. Plasmids with targeted fragments detected by colony PCR were extracted using a Plasmid Rapid Isolation Kit (Biodev-tech Company, Beijing, China). Five clones for each new allele were sequenced from both strands by SinoGenoMax Co., Ltd (Beijing, China).

Multiple alignments of sequences and translations of nucleotide sequences into amino acid sequences were performed by DNAMAN Version 6.0 software. Graphical data of sequencing results were analyzed by Chromas Version 1.4.5.

Real-time quantitative reverse transcription PCR

A total RNA of 4 wheat cultivars with different Vrn-B3 alleles were extracted from 2-month-old seedlings according to the method of Chen et al. [30]. DNA was removed by digestion with DNAse I (Qiagen, China) before reverse transcription. First-stand cDNA was synthesized using M-MLV transcriptase (Invitrogen, Carlsbad, CA, USA). Coding regions of different Vrn-B3 alleles in cDNA were sequenced with the Vrn-P15F/R primer set (Table 1) in order to confirm no sequence change in coding regions of the 4 Vrn-B3 alleles surveyed. The primer set Vrn-B3-RT_F/R (Table 1) was designed by Software Primer Premier 5.0 for RT-PCR amplification. Amplification with β-actin primers (Table 1) was used as an internal control to normalize all data. The relative quantification method (2-ΔΔCT) was used to evaluate quantitative variation between the 3 replicates, following the method of Livak and Schmittgen [38].

Notes

Abbreviations

Vrn: 

Vernalization

Ppd: 

Photoperiod

CNV: 

Copy number variation

PCR: 

Polymerase chain reaction

TE: 

Transposable element

CCT: 

CONSTANS, CO-like, and TOC1

UTR: 

Un-translate region

DH: 

Days to heading

DF: 

Days to flowering.

Declarations

Acknowledgements

The authors thank Dr. Chengxia Li (University of California, Davis) for review of this paper.

Funding

This project was funded by the 973 projects (2014CB138105), National Natural Science Foundation (31370031), and Program for New Century Excellent Talents in University (NCET-13-0776) & Technology Innovation Talents Program in Universities of Henan Province (2012HASTIT007) of China.

Authors’ Affiliations

(1)
Agronomy College, Henan Agricultural University
(2)
Key Laboratory of Physiological Ecology and Genetic Improvement of Food Crops in Henan Province
(3)
Collaborative Innovation Center of Henan Grain Crops

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