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黄热病蚊子埃及伊蚊的卵黄膜基因。

Vitelline envelope genes of the yellow fever mosquito, Aedes aegypti.

作者信息

Edwards M J, Severson D W, Hagedorn H H

机构信息

Department of Genetics, Case Western Reserve University, Cleveland, OH 44106, USA.

出版信息

Insect Biochem Mol Biol. 1998 Dec;28(12):915-25. doi: 10.1016/s0965-1748(98)00083-6.

Abstract

Vitelline envelope genes from the mosquito Aedes aegypti were analyzed with respect to their DNA sequences, genomic representation, temporal and spatial expression profiles and response to 20-hydroxyecdysone. Genomic clones of three vitelline envelope genes, 15a-1, 15a-2 and 15a-3 were isolated. Southern analysis indicates that all three genes are represented by a single copy in the genome. The deduced amino acid sequences of all three vitelline envelope genes contain a conserved region of 46 residues that overlaps with a region that is conserved in four Drosophila melanogaster vitelline envelope genes. DNA was sequenced flanking the 15a-1, 15a-2 and 15a-3 coding regions. A 360 bp sequence 5' of the 15a-2 coding region was identified with 72% identity to a sequence upstream of the Ae. aegypti VgA1 vitellogenin gene. The temporal patterns of 15a-1, 15a-2 and 15a-3 expression, as determined by Northern analysis, were similar. The spatial patterns of expression, as determined by whole-mount in situ hybridization, differed between the three genes. 15a-1 and 15a-3 were only expressed in the middle and posterior regions of the follicle, while 15a-2 was also expressed at the anterior region. Vitelline envelope gene expression was higher in ovaries that were dissected at 0, 2 and 10 h following a blood meal and then incubated in vitro for 10 h in medium containing 10(-5) M 20-hydroxyecdysone, compared to ovaries that were incubated without hormone.

摘要

对埃及伊蚊卵黄膜基因的DNA序列、基因组呈现、时空表达谱以及对20-羟基蜕皮酮的反应进行了分析。分离出了三个卵黄膜基因15a-1、15a-2和15a-3的基因组克隆。Southern分析表明,这三个基因在基因组中均由单拷贝代表。所有三个卵黄膜基因推导的氨基酸序列都包含一个46个残基的保守区域,该区域与四个黑腹果蝇卵黄膜基因中保守的一个区域重叠。对15a-1、15a-2和15a-3编码区两侧的DNA进行了测序。在15a-2编码区5'端鉴定出一个360 bp的序列,与埃及伊蚊VgA1卵黄原蛋白基因上游的一个序列有72%的同一性。通过Northern分析确定的15a-1、15a-2和15a-3表达的时间模式相似。通过整体原位杂交确定的表达空间模式在这三个基因之间有所不同。15a-1和15a-3仅在卵泡的中部和后部区域表达,而15a-2也在前部区域表达。与未用激素孵育的卵巢相比,在血餐后0、2和10小时解剖并在含有10(-5) M 20-羟基蜕皮酮的培养基中体外孵育10小时的卵巢中,卵黄膜基因的表达更高。

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