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果蝇OVO锌指蛋白调控ovo和卵巢肿瘤靶基因启动子。

Drosophila OVO zinc-finger protein regulates ovo and ovarian tumor target promoters.

作者信息

Lü J, Andrews J, Pauli D, Oliver B

机构信息

The Laboratory of Cellular and Developmental Biology, NIDDK, National Institutes of Health, Bethesda Maryland 20892, USA.

出版信息

Dev Genes Evol. 1998 Jun;208(4):213-22. doi: 10.1007/s004270050175.

Abstract

The ovo+ and ovarian tumor+ genes function in the germline sex determination pathway in Drosophila, but the hierarchical relationship between them is unknown. We found that increased ovo+ copy number resulted in increased ovarian tumor expression in the female germline and increased ovo expression in the male germline. The ovo locus encodes C2H2 zinc-finger proteins. Bacterially expressed OVO zinc-finger domain bound to multiple sites at or near the ovo and ovarian tumor promoters strongly suggesting that OVO is directly autoregulatory and that ovarian tumor is a direct downstream target of ovo in the germline sex determination hierarchy. Both positive and negative regulation by OVO proteins appears likely, depending on promoter context and on the sex of the fly. Our observation that two strong OVO-binding sites are at the initiator of the TATA-less ovo-B and ovarian tumor promoters raises the possibility that OVO proteins influence the nucleation of transcriptional pre-initiation complexes.

摘要

ovo+基因和卵巢肿瘤+基因在果蝇的生殖系性别决定途径中发挥作用,但它们之间的层级关系尚不清楚。我们发现,ovo+拷贝数增加会导致雌性生殖系中卵巢肿瘤表达增加,以及雄性生殖系中ovo表达增加。ovo基因座编码C2H2锌指蛋白。细菌表达的OVO锌指结构域与ovo和卵巢肿瘤启动子处或其附近的多个位点结合,强烈表明OVO直接进行自我调节,并且在生殖系性别决定层级中卵巢肿瘤是ovo的直接下游靶点。根据启动子背景和果蝇的性别,OVO蛋白似乎既有正调控作用也有负调控作用。我们观察到两个强OVO结合位点位于无TATA的ovo-B和卵巢肿瘤启动子的起始位点,这增加了OVO蛋白影响转录前起始复合物成核的可能性。

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