Lignin metabolism plays a pivotal role in
plant defense against pathogens and is always positively correlated as a
response to pathogen infection. Thus,
understanding resistance genes against pathogens in plants depends on a genetic
analysis of lignin response. In the
study, eight upland cotton lines were used to construct a multi-parent advanced
generation intercross (MAGIC) population (n=280),
which exhibited peculiar characteristics from the convergence of various
alleles coding for advantageous traits. To measure the lignin response to Verticillium wilt (LRVW), artificial disease nursery (ADN) and rotation nursery (RN) were
prepared for MAGIC population planting in four environments. The stem lignin contents were collected, and
the LRVW was measured with the lignin value of ADN/RN in each environment,
which showed great variation. A total of
9323 high-quality single-nucleotide polymorphism (SNP) markers obtained from
the Cotton-SNP63K array were employed for genotyping the MAGIC population. The SNPs were distributed through the whole
genome with 4.78 SNP/Mb density, ranging from 1.14 (ChrA06) to 10.08 (ChrD08). A genome-wide association study was performed
using a mixed linear model (MLM) for LRVW, and three stable quantitative trait
loci (QTLs), qLRVW-A04, qLRVW-A10 and qLRVW-D05, were identified in more than two environments. Two key candidate genes, Ghi_D05G01046 and Ghi_D05G01221, were selected within the QTLs through the combination
of variations in the coding sequence, induced expression patterns, and function
annotations, both of which presented nonsynonymous mutations in coding regions
and were strongly induced by Verticillium dahliae. Ghi_D05G01046 encodes a leucine-rich
extensin (LRx) protein, which is involved in Arabidopsis cell wall
biosynthesis and organization. Ghi_D05G01221 encodes a transcriptional co-repressor novel interactor of jaz (NINJA), which
functions in the jasmonic acid (JA) signaling pathway. In summary, the study creates valuable genetic
resources for breeding and QTL mapping and opens up a
new perspective to uncover the genetic basis of VW resistance in upland cotton.