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黑腹果蝇酯酶6基因5'启动子区域的核苷酸多态性及其与酶活性变异的关系。

Nucleotide polymorphism in the 5' promoter region of esterase 6 in Drosophila melanogaster and its relationship to enzyme activity variation.

作者信息

Odgers W A, Healy M J, Oakeshott J G

机构信息

CSIRO Division of Entomology, Canberra, Australia.

出版信息

Genetics. 1995 Sep;141(1):215-22. doi: 10.1093/genetics/141.1.215.

Abstract

A 974-bp region immediately 5' of the esterase 6 gene was sequenced in 17 field derived third chromosome isoallelic lines. Twenty-three polymorphisms were identified, only two in the first 400 bp 5' but 16 in a 325-bp region from -494 to -819 bp. This distribution differs from previously published patterns in Drosophila simulans and D. mauritiana, where the first 800 bp are highly conserved. Fourteen common polymorphisms in the 325-bp region above are all in strong linkage disequilibrium with each other. Moreover, most of the haplotypes defined by the total of 23 polymorphisms fall into two groups that differ as a block at all 14 of these latter sites. Sequence differences between the two groups include some restriction sites that were scored in an earlier study of RFLPs and EST6 enzyme phenotypes among 42 isoallelic lines from the same population. By collating the two studies, we show that one haplotype group yields approximately 15% lower EST6 enzyme activity in adult males than the other. The promoter haplotypes show only weak disequilibrium with the esterase 6 fast/slow allozyme polymorphism, so it seems unlikely that previously reported latitudinal clines in the allozyme frequencies are due to their hitchhiking along with selection on the promoter difference.

摘要

在17个源自野外的第三染色体等基因系中,对酯酶6基因5'端紧邻的一段974 bp区域进行了测序。共鉴定出23个多态性位点,其中5'端前400 bp中只有2个,而在-494至-819 bp的325 bp区域中有16个。这种分布与之前发表的拟果蝇和毛里求斯果蝇的模式不同,在那些模式中,前800 bp是高度保守的。上述325 bp区域中的14个常见多态性位点彼此之间都处于强连锁不平衡状态。此外,由总共23个多态性位点定义的大多数单倍型可分为两组,在这14个位点上,两组之间整体存在差异。两组之间的序列差异包括一些限制性位点,这些位点在对来自同一群体的42个等基因系的RFLP和EST6酶表型的早期研究中进行了评分。通过整理这两项研究,我们发现其中一个单倍型组在成年雄性中的EST6酶活性比另一个组低约15%。启动子单倍型与酯酶6快/慢等位酶多态性仅表现出微弱的不平衡,因此,先前报道的等位酶频率的纬度梯度似乎不太可能是由于它们与启动子差异上的选择搭便车所致。

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