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大麦旗叶抑制的遗传学

Genetics of barley hooded suppression.

作者信息

Roig Cristina, Pozzi Carlo, Santi Luca, Müller Judith, Wang Yamei, Stile Maria Rosaria, Rossini Laura, Stanca Michele, Salamini Francesco

机构信息

Max-Planck-Institut für Züchtungsforschung, 50829 Cologne, Germany.

出版信息

Genetics. 2004 May;167(1):439-48. doi: 10.1534/genetics.167.1.439.

DOI:10.1534/genetics.167.1.439
PMID:15166167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1470836/
Abstract

The molecular basis of the barley dominant Hooded (K) mutant is a duplication of 305 bp in intron IV of the homeobox gene Bkn3. A chemical mutagenesis screen was carried out to identify genetical factors that participate in Bkn3 intron-mediated gene regulation. Plants from recurrently mutagenized KK seeds were examined for the suppression of the hooded awn phenotype induced by the K allele and, in total, 41 suK (suppressor of K) recessive mutants were identified. Complementation tests established the existence of five suK loci, and alleles suKB-4, suKC-33, suKD-25, suKE-74, and suKF-76 were studied in detail. All K-suppressed mutants showed a short-awn phenotype. The suK loci have been mapped by bulked segregant analysis nested in a standard mapping procedure based on AFLP markers. K suppressor loci suKB, B, E, and F all map in a short interval of chromosome 7H, while the locus suKD is assigned to chromosome 5H. A complementation test between the four suK mutants mapping on chromosome 7H and the short-awn mutant lks2, located nearby, excluded the allelism between suK loci and lks2. The last experiment made clear that the short-awn phenotype of suK mutants is due to a specific dominant function of the K allele, a function that is independent from the control on hood formation. The suK loci are discussed as candidate participants in the regulation of Bkn3 expression.

摘要

大麦显性带帽(K)突变体的分子基础是同源异型盒基因Bkn3内含子IV中305 bp的重复。开展了化学诱变筛选,以鉴定参与Bkn3内含子介导的基因调控的遗传因子。检查经反复诱变的KK种子长成的植株,看其是否抑制了由K等位基因诱导的带帽芒表型,总共鉴定出41个suK(K的抑制子)隐性突变体。互补测验确定了5个suK位点的存在,并对suKB - 4、suKC - 33、suKD - 25、suKE - 74和suKF - 76等位基因进行了详细研究。所有K抑制的突变体均表现出短芒表型。已通过基于AFLP标记的标准作图程序嵌套的混合分离群体分析法对suK位点进行了定位。K抑制子位点suKB、B、E和F均定位在7H染色体的一个短区间内,而位点suKD定位于5H染色体。对定位在7H染色体上的4个suK突变体与附近的短芒突变体lks2之间进行的互补测验排除了suK位点与lks2之间的等位关系。最后一项实验表明,suK突变体的短芒表型是由于K等位基因的特定显性功能,该功能独立于对颖片形成的控制。讨论了suK位点作为Bkn3表达调控候选参与者的情况。

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