Skip to main content

Table 2 Chromosome locations and putative annotations of the PLUG markers

From: PCR-based landmark unique gene (PLUG) markers effectively assign homoeologous wheat genes to A, B and D genomes

  

Wheat chromosome

 

Marker no.

Type

undigested, 1% agarose

Hae III-digest, 4% agarose

Taq I-digest, 4% agarose

Annotation of orthologous rice gene (Pseudomolecules ver. 4)

1

III

  

3A, 3B, 3D

Phospholipase/Carboxylesterase family protein

2

III

 

3A, 3B

3A, 3B

Elicitor-responsive protein 1, putative

3

II

6B

6B

6A, 6B, 6D

GTP-binding protein, putative

4

III

  

6B, 6D

expressed protein

5

III

 

5A, 4D

5A, 4D

CIPK-like protein 1, putative

6

III

   

magnesium transporter CorA-like family protein, putative

7

III

   

Cysteine synthase, chloroplast precursor, putative

8

III

 

2A, 2B, 2D

2B

RNA recognition motif family protein

9

III

  

1A, 1B, 1D

AML6, putative

10

I

1A, 1B, 1D

1A, 1B, 1D

1A

chlorophyll synthase, ChlG family protein

11

III

 

7A, 7D

 

senescence-associated protein, putative

12

I

7A, 7B, 7D

7A, 7B, 7D

7A, 7B, 7D

Polyprenyl synthetase family protein

13

III

  

3A, 5A, 5D

Phosphatidylinositol N-acetylglucosaminyltransferase subunit A, putative

14

III

   

COP9 signalosome complex subunit 7, putative

15

III

 

7A

7B, 7D

MSP domain containing protein

16

II

7B

 

7B

expressed protein

17

III

  

7A

BadF/BadG/BcrA/BcrD ATPase family protein

18

II

5A

5A, 5B

5A, 5B, 5D

Triosephosphate isomerase, chloroplast precursor, putative

19

II

1A

1B, 1D

1A, 1B, 1D

ATP synthase gamma chain, mitochondrial precursor, putative

20

III

 

1A

1A

PRP19/PSO4 homolog, putative

21

III

   

Ubiquinol-cytochrome c reductase complex 7.8 kDa protein, putative

22

III

   

Small GTP-binding protein domain containing protein

23

III

 

5A

5B

Aspartyl aminopeptidase, putative

24

II

5B

5A, 5B, 5D

5A, 5B

expressed protein

  1. Types I, II and III indicate that 1% agarose gel electrophoresis of PCR products resulted in the separation of three, two, or single bands, respectively. PLUG markers were assigned to chromosomes by electrophoresis on 1% agarose gels, or by electrophoresis of Hae III- or Taq I-digested fragments on 4% agarose gels. The table also shows the annotations of TaEST-LUGs that were used for marker development.