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Table 5 Verification of prediction by experimental analysis

From: Prediction of transcriptional regulatory elements for plant hormone responses based on microarray data

AGI code

Position from TSS1

RARf

Predicted cis-element

REG

Prediction assessment

Reference4

Response

Element name

MEME

Gibbs Sampler

  

Drought2

SA3

        

AT5G52310

(RD29A)

-231

3.12

 

ATACCGACATCA

 

Positive

Yamaguchi-Shinozaki, 1994

Drought

DRE

No detect.

No detect.

 

-175

3.94

 

ACTACCGACATGAG

 

Positive

Narusaka, 2003

Drought

DRE

No detect.

No detect.

 

-137

4.22

 

AAGCCGACACA

 

Positive

Narusaka, 2003

Drought

DRE-core

No detect.

No detect.

 

-125

3.76

 

ACACGCGTAGA

AtREG536

?5

Narusaka, 2003

Drought

 

No detect. 7

No detect.

 

-82

3.44

 

ACAGACGC

 

False positive

Yamaguchi-Shinozaki, 1994

Drought

 

No detect

No detect

 

-71

5.01

 

ATACGTGTCCCT

AtREG557,472

Positive

Narusaka, 2003

Drought

ABRE

No detect.

No detect.7

AT5G52300

(RD29B)

-163

3.16

 

CGTACGTGTCA

AtREG450

False positive

Uno, 2000

Drought

 

No detect

No detect7

 

-137

*

   

Absent 7

Uno, 2000

Drought

ABRE

No detect.

No detect.7

 

-112

3.21

 

GTACGTGTCA

AtREG557, 389

Positive

Uno, 2000

Drought

ABRE

No detect.

No detect. 7

AT2G14610

(PR1)

-669

 

3.82

ACGTCACT

 

Positive

Pape, 2010

INA6/SA

LS5

No detect.

No detect.

 

-657

 

6.38

TACTTACGTCAT

 

Positive

Lebel, 1998; Pape, 2010

INA6/SA

LS7

No detect.

No detect.

 

-607

 

3.65

TAGGCAAG

 

False positive

Lebel, 1998

INA6/SA

 

No detect

No detect

  1. 1Position from major TSS data from ppdb. 21 h-treatment. 3See Table 3 for experimental conditions. 4Source of functional analysis. *RARf for ABA response is 3.7. 5Lack of the corresponding functional data. 6INA: 2,6-dichloro isonicotinic acid, a SA analog. 7Detected with the promoter set of ABA response. For analysis of RD29B by MEME and Gibbs Sampler, it was included to the applied promoter set. Promoter scan for prediction was achieved for the regions where linker scan or intensive functional analyses were achieved, and peaks with RARf > 3.0 were selected as prediction. Utilized RARf tables are shown in the table.