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果蝇黑腹果蝇嘧啶营养缺陷型与残基位点的互补图谱。

Pyrimidine auxotrophy and the complementation map of the rudimentary locus of Drosophila melanogaster.

作者信息

Falk D R

出版信息

Mol Gen Genet. 1976 Oct 18;148(1):1-8. doi: 10.1007/BF00268539.

Abstract

The complementation pattern of twelve rudimentary mutations have been analyzed at two different levels. When analyzed on the basis of complementation for a wing abnormality the mutations can be divided into three groups, each of which is believed to affect the activity of one of the first three enzymes of pyrimidine synthesis (Norby, 1973; Jarry and Falk, 1974; Rawls and Fristrom, 1975). However, when the mutants are analyzed for complementation on the basis of a second phenotype, pyrimidine auxotrophy, the distinction between two of these three groups is not evident. The disparity in the two patterns probably reflects a different threshold of gene activity required for the detection of an auxotrophic phenotype as compared to that at which a wing abnormality is detectable. The biochemical basis of these results is interpreted in light of recent data suggesting that at least the first two enzymes of pyrimidine synthesis are contained within a single multifunctional protein complex (Soderholm et al., 1975).

摘要

已在两个不同层面分析了12种残翅突变的互补模式。基于翅膀异常互补进行分析时,这些突变可分为三组,每组被认为影响嘧啶合成的前三种酶之一的活性(诺比,1973;贾里和福尔克,1974;罗尔斯和弗里斯特罗姆,1975)。然而,当根据第二种表型,即嘧啶营养缺陷型对突变体进行互补分析时,这三组中的两组之间的区别并不明显。这两种模式的差异可能反映了与可检测到翅膀异常时相比,检测营养缺陷型表型所需的基因活性阈值不同。根据最近的数据对这些结果的生化基础进行了解释,这些数据表明嘧啶合成的至少前两种酶包含在一个单一的多功能蛋白质复合物中(索德霍尔姆等人,1975)。

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