2020
DOI: 10.1104/pp.19.01531
|View full text |Cite
|
Sign up to set email alerts
|

The Ligon lintless-2 Short Fiber Mutation Is Located within a Terminal Deletion of Chromosome 18 in Cotton

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
22
0

Year Published

2020
2020
2024
2024

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 20 publications
(26 citation statements)
references
References 84 publications
1
22
0
Order By: Relevance
“…Enrichment of DEGs at the N 5 locus and its flanking regions indicates the existence of a cluster of co-regulated and functionally related genes associated with the mutant phenotype. A similar phenomenon has been reported for the genomic region with the Ligon lintless-2 mutation ( Patel et al 2020 ). One possibility for co-regulation of functionally related genes is the presence of shared cis -regulatory elements in their promoters.…”
Section: Resultssupporting
confidence: 85%
“…Enrichment of DEGs at the N 5 locus and its flanking regions indicates the existence of a cluster of co-regulated and functionally related genes associated with the mutant phenotype. A similar phenomenon has been reported for the genomic region with the Ligon lintless-2 mutation ( Patel et al 2020 ). One possibility for co-regulation of functionally related genes is the presence of shared cis -regulatory elements in their promoters.…”
Section: Resultssupporting
confidence: 85%
“…However, this compensation may not be highly effective because the yield traits of E6015‐3S, which lacked TaHST1 and carried extensive deletions in 4AL distal terminus, were decreased under control conditions in the field relative to those of E6015‐4T (Table S1). In line with this proposition, a recent study in tetraploid cotton shows that the functional deficiency of two glycosyltransferase genes, caused by a terminal deletion in the short arm of chromosome 18, could not be compensated by their homoeologs, thus leading to a defective short fibre phenotype (Patel et al, 2020). From this finding and the contrasting performance of E6015‐3S and E6015‐4T under field conditions (Figure 2), we reckon that the deletions in 4AL distal end should be corrected timely so as to enhance wheat tolerance to more severe HS episodes that are likely to occur in the coming years because of global warming (Lesk et al, 2016; Reinman, 2013).…”
Section: Discussionmentioning
confidence: 89%
“…The Li 1 mutation is caused by a Gly65Val substitution in an actin gene on chromosome D04, which disrupts cell polarity and F-actin organization resulting in dwarf, lintless cotton plants [ 15 ]. The Li 2 mutation is located within a terminal deletion of chromosome 18 (also called chromosome D13) [ 18 ]. A comparative study shows that at least seven of the 10 putative fiber development genes in the deletion region showed a higher expression in the wild type than in a Li 2 mutant during the fiber development stages.…”
Section: Introductionmentioning
confidence: 99%
“…However, no statistically significant ( p > 0.05) difference in the parameter of micronaire is observed between the two cotton fibers. Those morphological characterizations helped the genomic studies shed novel light on cotton fiber elongation, suggesting multiple genes coordinately regulated processes involving cell wall development and cell elongation [ 18 ].…”
Section: Introductionmentioning
confidence: 99%