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异源多倍体小麦中同源配对(ph)突变体的核型稳定性分析。

Analysis of karyotypic stability of homoeologous-pairing (ph) mutants in allopolyploid wheats.

作者信息

Sánchez-Morán E, Benavente E, Orellana J

机构信息

Unidad de Genética, Departamento de Biotecnología, ETSI Agrónomos, Universidad Politécnica de Madrid, Spain.

出版信息

Chromosoma. 2001 Sep;110(5):371-7. doi: 10.1007/s004120100156.

Abstract

Karyotypic analysis of wheat lines with different genotypes for the homoeologous-pairing loci Ph1 and Ph2 was carried out by means of a genomic in situ hybridization method that allowed unequivocal identification of the A, B and D genomes. Chromosomal rearrangements mainly affecting the A and D genomes were found in all plants of allohexaploid wheat (AABBDD) lacking Ph1 activity. The frequency of intergenomic exchanges per plant in ph1b mutant and nulli-5B lines was 4.31 and 3.40, respectively. In addition, an unbalanced genomic constitution was found in a few plants, some even showing a euploid chromosomal number. By contrast, rearranged karyotypes were detected neither in the ph1 mutant line (ph1c) of allotetraploid wheat (AABB) nor in the allohexaploid wheat lines lacking Ph2 activity, namely ph2b mutant and nulli-3D lines. These results were compared with the chromosomal pairing behaviour displayed by mutant lines ph1c, ph1b and ph2b at first meiotic metaphase. Despite the finding of standard, nonrearranged karyotypes in the phlc tetraploid mutant, the frequency of A-B homoeologous metaphase I association was similar to that observed in the ph1b hexaploid mutant. The results presented clearly demonstrate that inactivity of the Ph1 locus induces karyotypic instability in wheat. Intergenomic exchanges have probably been accumulating since the original ph1 mutant and aneuploid lines were obtained, which should be taken into account when it is planned to use these lines for basic research on Ph1 function or in applied wheat breeding programmes.

摘要

利用基因组原位杂交方法对具有不同同源配对位点Ph1和Ph2基因型的小麦品系进行了核型分析,该方法能够明确鉴定A、B和D基因组。在所有缺乏Ph1活性的异源六倍体小麦(AABBDD)植株中均发现了主要影响A和D基因组的染色体重排。ph1b突变体和缺失5B染色体的品系中,单株基因组间交换频率分别为4.31和3.40。此外,在少数植株中发现了基因组组成不平衡的情况,有些植株甚至显示出整倍体染色体数。相比之下,在异源四倍体小麦(AABB)的ph1突变系(ph1c)以及缺乏Ph2活性的异源六倍体小麦品系(即ph2b突变体和缺失3D染色体的品系)中均未检测到重排核型。将这些结果与ph1c、ph1b和ph2b突变系在第一次减数分裂中期的染色体配对行为进行了比较。尽管在ph1c四倍体突变体中发现了标准的、未重排的核型,但其A - B同源染色体在减数分裂中期I的联会频率与ph1b六倍体突变体中观察到的频率相似。所呈现的结果清楚地表明,Ph1位点的失活会诱导小麦核型不稳定。自最初获得ph1突变体和非整倍体系以来,基因组间的交换可能一直在积累,在计划将这些品系用于Ph1功能的基础研究或应用小麦育种计划时应予以考虑。

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