Suppr超能文献

影响间接飞行肌肌原纤维蛋白的果蝇飞行缺失突变体的分离。

Isolation of Drosophila flightless mutants which affect myofibrillar proteins of indirect flight muscle.

作者信息

Mogami K, Hotta Y

出版信息

Mol Gen Genet. 1981;183(3):409-17. doi: 10.1007/BF00268758.

Abstract

A large number of dominant flightless mutants of Drosophila were chemically induced, and their thorax proteins were examined by chemically induced, and their thorax proteins were examined by means of two-dimensional gel electrophoresis (O'Farrell 1975). Among them, 26 lines were found to have deficiency or reduction of some of myofibrillar proteins in indirect flight muscle (IFM). The gel patterns of the mutants could be classified into eleven groups. In general, more than a few polypeptides were either absent or reduced in each mutant line. Although the mutations affect myofibrillar proteins in apparently complex and diverse ways, logical correlations were found among the changes. There are pairs of proteins which always change together when a number of mutants are compared. There are also many pairs in which presence of one protein is necessary, but not sufficient for presence of the other. This suggests that absence of one component leads to disappearance or reduction of others which are either spatially or functionally related to the former. The correlation is possibly due to a hierarchy of the proteins in the myofibrillar assembly processes. Chromosomal loci of eleven typical mutants were examined, and it was found that most of them are located in two small regions of the second and the third chromosomes. IFM myofibrils of these mutants are either abnormal or absent in homozygotes as well as in heterozygotes.

摘要

通过化学方法诱导出了大量果蝇显性无飞行能力突变体,并借助二维凝胶电泳技术(奥法雷尔,1975年)对其胸部蛋白质进行了检测。在这些突变体中,发现有26个品系的间接飞行肌(IFM)中的一些肌原纤维蛋白存在缺失或减少的情况。突变体的凝胶图谱可分为11组。一般来说,每个突变品系中都有不止几条多肽链缺失或减少。尽管这些突变以明显复杂多样的方式影响肌原纤维蛋白,但在这些变化之间发现了合乎逻辑的相关性。在比较多个突变体时,有几对蛋白质总是一起发生变化。也有许多对蛋白质,其中一种蛋白质的存在是另一种蛋白质存在的必要条件,但不是充分条件。这表明一种成分的缺失会导致其他在空间或功能上与前者相关的成分消失或减少。这种相关性可能是由于肌原纤维组装过程中蛋白质的层次结构所致。对11个典型突变体的染色体位点进行了检测,发现它们中的大多数位于第二和第三染色体的两个小区域内。这些突变体的纯合子和杂合子的IFM肌原纤维均异常或缺失。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验