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神经母细胞瘤细胞中雄激素控制的特异性基因表达。

Androgen-controlled specific gene expression in neuroblastoma cells.

作者信息

Yerramilli-Rao P, Garofalo O, Whatley S, Leigh P N, Gallo J M

机构信息

Department of Neurology, Institute of Psychiatry, Denmark Hill, London, UK.

出版信息

J Neurol Sci. 1995 May;129 Suppl:131-5. doi: 10.1016/0022-510x(95)00083-e.

Abstract

In Kennedy's syndrome, a mutation in the androgen receptor (AR) gene leads to sensory and lower motor neurone degeneration, therefore genes that are regulated by androgens in neurones may be important in the process of motor neurone cell death. The aim of this study was to identify androgen-inducible genes in the human neuroblastoma cell line SH-SY5Y. We have shown that SH-SY5Y cells expressed the AR by Northern blot analysis using a 32P-labelled probe derived from a human AR cDNA. Differential display of mRNAs has been used to identify and clone putative genes that are regulated by androgens in SH-SY5Y cells. Nine cDNA fragments, ranging in size from 180 bp to 480 bp, corresponding to mRNA species which appear to be differentially expressed in response to 5 alpha dihydrotestosterone (DHT), have been successfully cloned. These are now being sequenced and used as hybridisation probes for Northern blot analysis in order to confirm their induction by DHT. Characterisation of these genes may provide clues to the mechanisms of motor neurone degeneration.

摘要

在肯尼迪综合征中,雄激素受体(AR)基因突变会导致感觉和下运动神经元退化,因此,神经元中受雄激素调控的基因可能在运动神经元细胞死亡过程中起重要作用。本研究的目的是在人神经母细胞瘤细胞系SH-SY5Y中鉴定雄激素诱导基因。我们通过使用源自人AR cDNA的32P标记探针进行Northern印迹分析,已证明SH-SY5Y细胞表达AR。mRNA差异显示已用于鉴定和克隆SH-SY5Y细胞中受雄激素调控的假定基因。已成功克隆了9个大小从180 bp到480 bp不等的cDNA片段,它们对应于似乎因5α-二氢睾酮(DHT)而差异表达的mRNA种类。目前正在对这些片段进行测序,并用作Northern印迹分析的杂交探针,以确认它们是否受DHT诱导。对这些基因的表征可能为运动神经元退化的机制提供线索。

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