Journal of Cotton Research (May 2021)

Genome-wide association study of micronaire using a natural population of representative upland cotton (Gossypium hirsutum L.)

  • Jikun SONG,
  • Wenfeng PEI,
  • Jianjiang MA,
  • Shuxian YANG,
  • Bing JIA,
  • Yingying BIAN,
  • Yue XIN,
  • Luyao WU,
  • Xinshan ZANG,
  • Yanying QU,
  • Jinfa ZHANG,
  • Man WU,
  • Jiwen YU

DOI
https://doi.org/10.1186/s42397-021-00089-1
Journal volume & issue
Vol. 4, no. 1
pp. 1 – 12

Abstract

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Abstract Background Micronaire is a comprehensive index reflecting the fineness and maturity of cotton fiber. Micronaire is one of the important internal quality indicators of the cotton fiber and is closely related to the value of the cotton fiber. Understanding the genetic basis of micronaire is required for the genetic improvement of the trait. However, the genetic architecture of micronaire at the genomic level is unclear. The present genome-wide association study (GWAS) aimed to identify the genetic mechanism of the micronaire trait in 83 representative upland cotton lines grown in multiple environments. Results GWAS of micronaire used 83 upland cotton accessions assayed by a Cotton 63 K Illumina Infinium single nucleotide polymorphism (SNP) array. A total of 11 quantitative trait loci (QTLs) for micronaire were detected on 10 chromosomes. These 11 QTLs included 27 identified genes with specific expression patterns. A novel QTL, qFM-A12–1, included 12 significant SNPs, and GhFLA9 was identified as a candidate gene based on haplotype block analysis and on strong and direct linkage disequilibrium between the significantly related SNPs and gene. GhFLA9 was expressed at a high level during secondary wall thickening at 20∼25 days post-anthesis. The expression level of GhFLA9 was significantly higher in the low micronaire line (Msco-12) than that in the high micronaire line (Chuangyou-9). Conclusions This study provides a genetic reference for genetic improvement of cotton fiber micronaire and a foundation for verification of the functions of GhFLA9.

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