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导致种内水稻杂交杂种衰败的互补隐性基因的鉴定与连锁图谱构建

Identification and linkage mapping of complementary recessive genes causing hybrid breakdown in an intraspecific rice cross.

作者信息

Matsubara K, Ando T, Mizubayashi T, Ito S, Yano M

机构信息

National Institute of Agrobiological Sciences, 2-1-2 Kannondai, Tsukuba, Ibaraki, 305-8602, Japan.

出版信息

Theor Appl Genet. 2007 Jul;115(2):179-86. doi: 10.1007/s00122-007-0553-x. Epub 2007 May 8.

Abstract

One outcome of hybrid breakdown is poor growth, which we observed as a reduction in the number of panicles per plant and in culm length in an F(2) population derived from a cross between the genetically divergent rice (Oryza sativa L.) cultivars 'Sasanishiki' (japonica) and 'Habataki' (indica). Quantitative trait locus (QTL) analysis of the two traits and two-way ANOVA of the detected QTLs suggested that the poor growth was due mainly to an epistatic interaction between genes at QTLs located on chromosomes 2 and 11. The poor growth was likely to result when a plant was homozygous for the 'Habataki' allele at the QTL on chromosome 2 and homozygous for the 'Sasanishiki' allele at the QTL on chromosome 11. The results suggest that the poor growth found in the F(2) population was due to hybrid breakdown of a set of complementary genes. To test this hypothesis and determine the precise chromosomal location of the genes causing the hybrid breakdown, we performed genetic analyses using a chromosome segment substitution line, in which a part of chromosome 2 from 'Habataki' was substituted into the genetic background of 'Sasanishiki'. The segregation patterns of poor growth in plants suggested that both of the genes underlying the hybrid breakdown were recessive. The gene on chromosome 2, designated hybrid breakdown 2 (hbd2), was mapped between simple sequence repeat markers RM3515 and RM3730. The gene on chromosome 11, hbd3, was mapped between RM5824 and RM1341.

摘要

杂种衰败的一个结果是生长不良,我们在一个由遗传差异较大的水稻(Oryza sativa L.)品种“笹锦”(粳稻)和“羽咋”(籼稻)杂交产生的F(2)群体中观察到,每株植物的穗数和茎长减少。对这两个性状进行数量性状基因座(QTL)分析以及对检测到的QTL进行双向方差分析表明,生长不良主要是由于位于第2和第11号染色体上的QTL基因之间的上位性相互作用。当植株在第2号染色体上的QTL处为“羽咋”等位基因纯合,且在第11号染色体上的QTL处为“笹锦”等位基因纯合时,就可能导致生长不良。结果表明,F(2)群体中发现的生长不良是由于一组互补基因的杂种衰败所致。为了验证这一假设并确定导致杂种衰败的基因的确切染色体位置,我们使用染色体片段代换系进行了遗传分析,其中“羽咋”的第2号染色体的一部分被代换到“笹锦”的遗传背景中。植株中生长不良的分离模式表明,导致杂种衰败的两个基因均为隐性。位于第2号染色体上的基因命名为杂种衰败2(hbd2),定位在简单序列重复标记RM3515和RM3730之间。位于第11号染色体上的基因hbd3,定位在RM5824和RM1341之间。

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