ArticleTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik2025
A plastid lipid-associated protein-encoding gene (GhPAP) that positively regulates fiber strength was identified via genetic mapping and transcriptomic analysis of a stable QTL on chromosome D06 of upland cotton.
Article in TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Multiple environmental test and genetic mapping jointly reveal genomic loci and associated genes underlying cotton Verticillium wilt resistance.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2026Article
- Genetic mapping and identification of a major quantitative trait locus associated with the high fiber strength introgressed from Gossypium barbadense.Plant cell reports · 2026Article
- Cotton genetic mapping for plant biotechnology: from markers to graph pan-genomes and sustainable breeding.Frontiers in plant science · 2026Review
- An alpha/beta-hydrolase-like gene (GhABH) is identified to be responsible for fiber quality from a multi-effect quantitative trait locus (QTL) on chromosome A06 of upland cotton.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2025Article
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Authors and funding
8 authors.
Funding
Abstract
key messageGhPAP was identified as a candidate gene associated with cotton fiber development via genetic mapping and transcriptomic analysis. GhPAP increases fiber strength by modulating cell wall thickness and fiber helix formation. Cotton fiber strength (FS), length (FL), and fineness are economically important quality-related traits. Although many genes related to fiber quality were identified recently, the molecular mechanism controlling fiber quality remains largely unknown. In this study, an FS/FL-related stable QTL was mapped to a 2.92 Mb region containing 81 putative coding genes on chromosome D06 by combining SLAF-BSA-seq and InDel analyses of a bi-parental recombinant inbred line (RIL) population. Five genes in the QTL region were differentially expressed between two near-isogenic RILs, A
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