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黑腹果蝇中染色单体互换、姐妹染色单体交换和减数分裂重组之间的关系。

Relationships among chromatid interchanges, sister chromatid exchanges, and meiotic recombination in Drosophila melanogaster.

作者信息

Gatti M, Pimpinelli S, Baker B S

出版信息

Proc Natl Acad Sci U S A. 1980 Mar;77(3):1575-9. doi: 10.1073/pnas.77.3.1575.

Abstract

Repair- and recombination-defective mutations at two loci (mei-9 and mei-41) of Drosophila melanogaster have been examined for their effects on the induction of chromosome aberrations by x-rays and the formation of sister chromatid exchanges (SCEs). Irradiation of larval neuroblast cells during the S phase with x-rays showed that mutants at both of these loci are about 10 times more sensitive than wild type to the induction of chromosome aberrations. The pattern of induced aberrations was characteristic for each mutant locus: in cells bearing mei-9 mutations most breaks were chromatid deletions, whereas in the presence of mei-41 mutations similar frequencies of chromatid and isochromatid deletions were observed. Furthermore, chromatid interchanges could not be induced in cells carrying mei-9 alleles; therefore these mutations define a step necessary for chromatid rejoining. mei-41 alleles also define a function involved in the formation of chromatid interchanges; total exchanges were less frequent than expected from nonmutant controls; and the proportion of exchanges arising by symmetrical rejoining was markedly reduced. These data indicate that chromatid and isochromatid deletions have different molecular steps in their formation, and that different molecular mechanisms are also involved in the symmetrical and unsymmetrical rejoining in chromatid interchanges. Neuroblast cells of larvae bearing mei-9 and mei-41 alleles were also treated for 13 hr with 5-bromodeoxyuridine at 9 mug/ml in order to differentiate sister chromatids for the scoring of SCEs. Whereas mei-41 had a normal level of SCEs, mei-9 exhibited a frequency of SCEs that was about 70% that of the control. Because both mei-9 and mei-41 mutations result in defective meiotic recombination, these data suggest that they define steps shared by symmetrical interchange formation and meiotic recombination that do not participate in the formation of most SCEs.

摘要

对黑腹果蝇两个基因座(mei - 9和mei - 41)的修复和重组缺陷突变进行了研究,以考察它们对X射线诱导染色体畸变及姐妹染色单体交换(SCE)形成的影响。在S期用X射线照射幼虫神经母细胞,结果显示这两个基因座的突变体对染色体畸变诱导的敏感性比野生型高约10倍。每个突变基因座诱导的畸变模式都具有特征性:在携带mei - 9突变的细胞中,大多数断裂是染色单体缺失,而在存在mei - 41突变时,观察到染色单体和等臂染色单体缺失的频率相似。此外,携带mei - 9等位基因的细胞中不能诱导染色单体互换;因此这些突变定义了染色单体重新连接所必需的一个步骤。mei - 41等位基因也定义了一个参与染色单体互换形成的功能;总的交换频率低于非突变对照预期的值;并且通过对称重新连接产生的交换比例明显降低。这些数据表明染色单体和等臂染色单体缺失在形成过程中有不同的分子步骤,并且不同的分子机制也参与了染色单体互换中的对称和不对称重新连接。携带mei - 9和mei - 41等位基因的幼虫神经母细胞也用9μg/ml的5 - 溴脱氧尿苷处理13小时,以便区分姐妹染色单体以进行SCE评分。虽然mei - 41的SCE水平正常,但mei - 9的SCE频率约为对照的70%。由于mei - 9和mei - 41突变都导致减数分裂重组缺陷,这些数据表明它们定义了对称互换形成和减数分裂重组共有的、但不参与大多数SCE形成的步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b5/348539/a9159a8bcdb6/pnas00666-0354-a.jpg

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