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通过一种普遍适用于任何低表达基因的方法对插入序列IS10转座酶基因表达进行定量分析。

Quantitation of insertion sequence IS10 transposase gene expression by a method generally applicable to any rarely expressed gene.

作者信息

Raleigh E A, Kleckner N

出版信息

Proc Natl Acad Sci U S A. 1986 Mar;83(6):1787-91. doi: 10.1073/pnas.83.6.1787.

Abstract

We have found that IS10 transposase is synthesized in tiny amounts, about 0.15 polypeptide chain per cell per generation on average, as judged from the beta-galactosidase activity of a single chromosomal copy of a suitable transposase-lacZ gene fusion. Enzymatic activity from the fusion gene is a factor of 10 lower in a permeabilized whole cell assay than in cell extracts. Probably, most cells contain fewer than four polypeptide chains, and these chains can assemble into active tetramers only after cell disruption. This interpretation permits formulation of two equations relating enzyme activities to transcription and translation rates, solution of which reveals that the fusion gene is expressed at the average rate of only 0.25 transcript per cell per generation, with an average of only 0.58 translation product per transcript. This methodology is generally applicable to analysis of any gene from which fewer than four polypeptide chains are synthesized per cell per generation.

摘要

我们发现,IS10转座酶的合成量极少,根据合适的转座酶-lacZ基因融合的单个染色体拷贝的β-半乳糖苷酶活性判断,平均每代每个细胞约合成0.15条多肽链。在透化全细胞测定中,融合基因的酶活性比在细胞提取物中低10倍。可能大多数细胞含有的多肽链少于四条,并且这些链只有在细胞破裂后才能组装成有活性的四聚体。这种解释使得可以制定两个将酶活性与转录和翻译速率相关联的方程,求解这些方程表明融合基因的平均表达速率为每代每个细胞仅0.25个转录本,每个转录本平均只有0.58个翻译产物。这种方法通常适用于分析每代每个细胞合成少于四条多肽链的任何基因。

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