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在黑腹果蝇中,海恩酮诱导的X连锁隐性致死突变中多基因座缺失的比例很高。

High proportion of multi-locus deletions among hycanthone-induced X-linked recessive lethals in Drosophila melanogaster.

作者信息

Kramers P G, Schalet A P, Paradi E, Huiser-Hoogteyling L

出版信息

Mutat Res. 1983 Feb;107(2):187-201. doi: 10.1016/0027-5107(83)90162-8.

Abstract

328 X-linked recessive lethal mutations induced in late spermatids by hycanthone methanesulfonate were tested for coverage by duplications that comprised, in total, about 24% of the euchromatic X chromosome; 78 lethals appeared to be covered. Crossover localization tests of a random sample of 38 non-covered lethals revealed 4 chromosomes carrying a lethal within a duplicated segment. Lethals localized to a particular region were crossed to reference deficiencies and single-locus mutations, and inter se, to ascertain their genetic extent. The proportion of multi-locus deletions among these 78 covered and 4 non-covered lethals was 3/48, 1/10 and 13/24 for the distal, medial and proximal regions, respectively. A storage period of 9 days did not noticeably influence these proportions. In the sample of 38 non-covered lethals, and among 17 of the covered single-site lethals, 4 cases of strong crossover suppression were detected. Comparison of these results with data obtained with other mutagens suggests that induction of multi-locus deletions, and possibly of other types of chromosome rearrangement, could in part depend on other mechanisms than those acting in the formation of translocations and chromosome loss. For the purpose of mutagen testing, these findings imply that, in Drosophila, results in the regular genetic tests for chromosome breakage events do not always accurately predict the capacity of a mutagen to induce multi-locus deletions. This is of importance since transmissible multi-locus deletions have been considered a significant source of genetic damage in man.

摘要

对由甲磺酸海恩酮在晚期精子细胞中诱导产生的328个X连锁隐性致死突变进行了检测,看它们是否被总共覆盖约24%常染色质X染色体的重复序列所覆盖;78个致死突变似乎被覆盖。对38个未被覆盖的致死突变的随机样本进行交叉定位测试,发现4条染色体在重复片段内携带一个致死突变。将定位到特定区域的致死突变与参考缺失和单基因座突变进行杂交,并相互杂交,以确定它们的遗传范围。在这78个被覆盖和4个未被覆盖的致死突变中,多基因座缺失在远端、中间和近端区域的比例分别为3/48、1/10和13/24。9天的储存期对这些比例没有明显影响。在38个未被覆盖的致死突变样本以及17个被覆盖的单位点致死突变中,检测到4例强交叉抑制。将这些结果与用其他诱变剂获得的数据进行比较表明,多基因座缺失以及可能其他类型的染色体重排的诱导,部分可能取决于不同于导致易位和染色体丢失形成的其他机制。就诱变剂测试而言,这些发现意味着,在果蝇中,常规染色体断裂事件遗传测试的结果并不总是能准确预测诱变剂诱导多基因座缺失的能力。这很重要,因为可传递的多基因座缺失被认为是人类遗传损伤的一个重要来源。

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