Genome-wide association study of heat stress-tolerance traits in spring-type Brassica napus L. under controlled conditions

被引:2
作者
Mizanur Rahaman [1 ]
Sujan Mamidi [2 ]
Mukhlesur Rahman [1 ]
机构
[1] Department of Plant Sciences, North Dakota State University
[2] Hudson Alpha Institute for Biotechnology
关键词
Brassica napus; Heat stress; Controlled environment; QTL;
D O I
暂无
中图分类号
S565.4 [油菜籽(芸薹)];
学科分类号
0901 ;
摘要
High temperatures have a detrimental effect on growth, development, and yield of Brassica napus. Even a short period of heat stress can lead to yield losses of 15%–20%. A collection of spring-type accessions available in Germplasm Resources Information Network(GRIN)were used to assess the effect of short periods of high-temperature stress at the early flowering stage of B. napus. Two sets of accessions with three replications per set were grown in a greenhouse at 22/18 °C day/night temperatures. Plants from the second set at the 6-day flowering stage were exposed to heat-stress conditions(maximum temperature up to 35 °C) in a plant growth chamber for five days. The heat-stressed plants were then allowed to recover in a greenhouse. Pollen sterility, sterile/aborted pods, and number of pods on main raceme were recorded for both control(set 1) and heat stressed(set 2) plants.Heat susceptibility indices for all three traits were calculated and an association-mapping study was conducted using 37,539 Single Nucleotide Polymorphisms(SNPs) to identify genomic regions controlling the heat stress traits. A total of 5, 8, and 7 quantitative trait loci(QTL) were associated with pollen sterility, sterile/aborted pods, and number of pods on main raceme, respectively. Together they explained respectively 46.3%, 60.5%, and 60.6% of phenotypic variation. Candidate genes in the QTL regions included genes associated with flowering, male sterility, pollen abortion, embryo abortion reducing pollen development,and pod development.
引用
收藏
页码:115 / 125
页数:11
相关论文
共 17 条
  • [1] The arabidopsis information resource: Making and mining the “gold standard” annotated reference plant genome[J] . Tanya Z. Berardini,Leonore Reiser,Donghui Li,Yarik Mezheritsky,Robert Muller,Emily Strait,Eva Huala.genesis . 2015 (8)
  • [2] A Classification of Basic Helix-Loop-Helix Transcription Factors of Soybean[J] . Karen A. Hudson,Matthew E. Hudson,Martine A. Collart.International Journal of Genomics . 2015
  • [3] Natural Variations and Genome-Wide Association Studies in Crop Plants[J] . Xuehui Huang,Bin Han.Annual Review of Plant Biology . 2014
  • [4] The Role of Two F-Box Proteins, SLEEPY1 and SNEEZY, in Arabidopsis Gibberellin Signaling1[C][W][OA][J] . Ariizumi,Tohru,Lawrence,Paulraj K,Steber,Camille M.Plant Physiology . 2011 (2)
  • [5] PHOSPHATIDIC ACID PHOSPHOHYDROLASE1 and 2 Regulate Phospholipid Synthesis at the Endoplasmic Reticulum in Arabidopsis[W][J] . Eastmond,Peter J,Quettier,Anne-Laure,Kroon,Johan T M,Craddock,Christian,Adams,Nicolette,Slabas,Antoni R.Plant Cell . 2010 (8)
  • [6] Arabidopsis Histone Lysine Methyltransferases[J] . Frédéric Pontvianne,Todd Blevins,Craig S. Pikaard.Advances in Botanical Research . 2010
  • [7] The effect of drought and heat stress on reproductive processes in cereals[J] . Plant, Cell & Environment . 2007 (1)
  • [8] A Fast and Flexible Statistical Model for Large-Scale Population Genotype Data: Applications to Inferring Missing Genotypes and Haplotypic Phase[J] . Paul Scheet,Matthew Stephens.The American Journal of Human Genetics . 2006 (4)
  • [9] Adaptation of crops to climate change through genotypic responses to mean and extreme temperatures[J] . A.J. Challinor,T.R. Wheeler,P.Q. Craufurd,C.A.T. Ferro,D.B. Stephenson.Agriculture, Ecosystems and Environment . 2006 (1)
  • [10] Species, ecotype and cultivar differences in spikelet fertility and harvest index of rice in response to high temperature stress[J] . P.V.V. Prasad,K.J. Boote,L.H. Allen,J.E. Sheehy,J.M.G. Thomas.Field Crops Research . 2005 (2)