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首页> 外文期刊>Chromosome research: An international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology >Identification and physical mapping of induced translocation breakpoints involving chromosome 1R in rye.
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Identification and physical mapping of induced translocation breakpoints involving chromosome 1R in rye.

机译:黑麦中涉及染色体1R的诱导易位断裂点的鉴定和物理作图。

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摘要

To obtain translocations involving specific chromosomes in rye, pollen of a line in which chromosome 1R has large C-bands on its two telomeres, but which lacks C-bands (or has very small ones) on the telomeres of the remaining chromosomes, was X-irradiated. All translocations involving the labelled chromosome (1R) could be easily recognized in C-banded mitotic metaphases. The non-labelled chromosome involved in each translocation was identified either from mitotic C-banding analysis or from the meiotic configurations observed in some specific progenies. A physical map including 40 translocation breakpoints has been developed by means of synaptonemal complex (SC) analysis of well-paired pachytene quadrivalents. The results agree with the hypothesis of chromosomes 2R to 7R having similar probabilities of participating in translocations with chromosome 1R. However, the locations of the breakpoints are not entirely random: an excess of translocation breakpoints located on the short arm of chromosome 1R wasobtained, and the two acentric translocated segments of each translocation show a trend towards having similar sizes. The possible reasons for these two non-random situations are discussed.
机译:为了获得涉及黑麦中特定染色体的易位,染色体1R的两个端粒具有大C带,而其余染色体的端粒却缺乏C带(或非常小的)的花粉为X。 -辐照。所有涉及标记染色体(1R)的易位都可以在C带状有丝分裂中期轻易识别。从有丝分裂C带分析或某些特定子代中观察到的减数分裂构型中,鉴定出每个易位中涉及的未标记染色体。通过对配对的粗线四价体的突触复合物(SC)分析,已开发出包括40个易位断点的物理图谱。该结果与2R至7R染色体具有与1R染色体易位的相似概率的假设相符。但是,断点的位置并非完全随机:获得了位于染色体1R短臂上的过量易位断点,并且每个易位的两个无心易位片段显示出具有相似大小的趋势。讨论了这两种非随机情况的可能原因。

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