Department of Genetics, Faculty of Biology and Environment Protection, University of Silesia, Jagiellonska 28, Katowice, Poland.
J Appl Genet. 2011 Aug;52(3):257-68. doi: 10.1007/s13353-011-0031-7. Epub 2011 Feb 8.
The aim of these studies was to characterize nucleotide substitutions leading to the phenotype of brassinosteroid-insensitive, semi-dwarf barley mutant 093AR. Two substitutions in the sequence of barley HvBRI1 gene, encoding leucine-rich repeats receptor kinase (LRR-RK), which participates in brassinosteroid (BR) signalling, were identified in this chemically-induced barley mutant of the cv. Aramir. The LRR-RK is a transmembrane protein phosphorylating downstream components. The identified substitutions CC>AA at positions 1760 and 1761 in the HvBRI1 gene of this mutant led to a missense mutation, causing the Thr-573 to Lys-573 replacement in the protein sequence. The threonine residue is situated in the distal part of a 70-amino acids island responsible for binding of BR molecules. As this residue is conserved among BRI1 protein homologs in Arabidopsis thaliana, Lycopersicon esculentum, Oryza sativa and Hordeum vulgare, it was postulated that this residue is crucial for the protein function. The genetic analyses indicated that the mutant 093AR was allelic to the spontaneous, semi-dwarf mutant uzu which carries A>G substitution at position 2612 of the HvBRI1 gene (GenBank acc. no. AB088206). A comparison of the genomic sequence of HvBRI1 in the mutants uzu, 093AR and in the cv. 'Aramir' confirmed the presence of the single-nucleotide A>G substitution at position 2612 in the sequence encoding kinase domain of HvBRI1 polypeptide in uzu, but not in 093AR mutant, indicating that a new allele of the HvBRI1 gene was identified.
这些研究的目的是描述导致油菜素内酯不敏感、半矮秆大麦突变体 093AR 表型的核苷酸取代。在 cv. Aramir 的化学诱导大麦突变体中,鉴定出编码富含亮氨酸重复受体激酶 (LRR-RK) 的大麦 HvBRI1 基因序列中的两个取代,该激酶参与油菜素内酯 (BR) 信号转导。LRR-RK 是一种跨膜蛋白,可磷酸化下游成分。在该突变体的 HvBRI1 基因中,第 1760 和 1761 位的 CC>AA 取代导致错义突变,导致蛋白序列中 Thr-573 替换为 Lys-573。苏氨酸残基位于负责结合 BR 分子的 70 个氨基酸岛的远端部分。由于该残基在拟南芥、番茄、水稻和大麦的 BRI1 蛋白同源物中保守,因此推测该残基对于蛋白质功能至关重要。遗传分析表明,突变体 093AR 与自发的、半矮秆突变体 uzu 等位,uzu 在 HvBRI1 基因的第 2612 位发生 A>G 取代(GenBank acc. no. AB088206)。比较突变体 uzu、093AR 和 cv. 'Aramir' 的 HvBRI1 基因组序列证实,uzu 中 HvBRI1 多肽激酶结构域编码序列中存在第 2612 位的单核苷酸 A>G 取代,但在 093AR 突变体中不存在,表明鉴定出了 HvBRI1 基因的一个新等位基因。