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Genetic and Phenotypic Analysis of lax1-6, a Mutant Allele of LAX PANICLE1 in Rice

机译:水稻LAX PANICLE1突变等位基因lax1-6的遗传和表型分析

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摘要

Proper function of the LAX1 gene is required for the development of axillary meristem in rice. Here, we report genetic and phenotypic characters of a novel recessive mutant allele of rice LAX1 gene, lax1-6, which showed abnormal panicle phenotypes with few numbers of elongated primary rachis branches. Beside typical lax mutant phenotype, abnormalities of lax1-6 mutant allele were observed with defect lemma and palea primordial in floral organs. The lax1-6 mutant locus was linked between SSR markers RM7594 and RM5389 on chromosome 1 with 1.02% and 1.0% recombination frequencies, respectively. Molecular analysis revealed that the lax1-6 mutant allele was caused by a transversion mutation of nucleotide T to G substitution that resulted in an amino acid substitution from serine (S) to alanine (A) at the 117(th) position from amino terminus of a basic helix-loop-helix protein coded by LAX1 gene. Furthermore, we found that the Oryza sativa indica type cv. IRRI347 contained 24 nucleotide deletion in the upstream sequence in the LAX1 gene, but this deletion did not influence panicle morphology, which demonstrated that the deletion is a polymorphism in rice. All together, the lax1-6 mutant is a newly identified allele of LAX1 gene displaying the abnormal axillary meristems and inflorescences in rice.
机译:LAX1基因的正常功能是水稻腋生分生组织发育所必需的。在这里,我们报告水稻LAX1基因lax1-6的新型隐性突变等位基因的遗传和表型特征,其显示出异常的穗表型和少量的初级原发轴突分支。除了典型的lax突变体表型,还观察到lax1-6突变体等位基因的异常,其中在花卉器官中具有缺陷外and和古原始。 lax1-6突变基因座分别以1.02%和1.0%的重组频率连接到1号染色体上的SSR标记RM7594和RM5389之间。分子分析表明,lax1-6突变体等位基因是由核苷酸T到G取代的转位突变引起的,该突变导致在丝氨酸(S)到氨基酸末端117(th)位的丝氨酸(S)变成丙氨酸(A)的氨基酸取代。 LAX1基因编码的基本螺旋-环-螺旋蛋白。此外,我们发现稻米c型cv。 IRRI347在LAX1基因的上游序列中含有24个核苷酸的缺失,但是这种缺失并不影响穗的形态,这表明该缺失是水稻的一种多态性。总之,lax1-6突变体是一个新近鉴定的LAX1基因等位基因,显示了水稻中异常的腋生分生组织和花序。

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