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人类γ-氨基丁酸B受体基因:互补DNA克隆、表达、染色体定位及基因组结构

Human gamma-aminobutyric acid B receptor gene: complementary DNA cloning, expression, chromosomal location, and genomic organization.

作者信息

Goei V L, Choi J, Ahn J, Bowlus C L, Raha-Chowdhury R, Gruen J R

机构信息

Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut 06517, USA.

出版信息

Biol Psychiatry. 1998 Oct 15;44(8):659-66. doi: 10.1016/s0006-3223(98)00244-3.

Abstract

BACKGROUND

The 6p21.3 region of human chromosome 6 is a genetic locus for schizophrenia, juvenile myoclonic epilepsy, and dyslexia.

METHODS

Due to our interest in these disorders we performed complementary DNA (cDNA) hybridization selection on genomic DNA clones spanning this region to identify potential positional-candidate genes.

RESULTS

We identified a full-length cDNA with an open reading frame of 2883 bp corresponding to a predicted protein of 961 amino acids that shares greater than 95% homology with the rat gamma-aminobutyric acid B (GABAB) receptor. Northern blot hybridization identified a 4.4-kb transcript in human brain. The human gene mapped to two sites on 6p21.3 separated by 2 Mb. Sequence analysis of both sites showed that the centromeric gene is transcribed, whereas the telomeric site is likely a pseudogene. The transcribed gene is distributed over 22 exons spanning 18 kb of genomic DNA.

CONCLUSIONS

The genomic location, tissue expression, and function of the human GABAB receptor gene suggest that it is an important positional-candidate for the neurobehavioral disorders with a genetic locus on 6p21.3. In addition, delineation of the genomic organization will now permit it to be integrated as part of pharmacogenetic studies in trials of anxiolytic, narcotic, antiepileptic, and fluoxetine therapies.

摘要

背景

人类6号染色体的6p21.3区域是精神分裂症、青少年肌阵挛性癫痫和诵读困难的一个基因位点。

方法

由于我们对这些疾病感兴趣,我们对跨越该区域的基因组DNA克隆进行了互补DNA(cDNA)杂交筛选,以鉴定潜在的定位候选基因。

结果

我们鉴定出一个全长cDNA,其开放阅读框为2883 bp,对应于一个预测的961个氨基酸的蛋白质,该蛋白质与大鼠γ-氨基丁酸B(GABAB)受体具有大于95%的同源性。Northern印迹杂交在人脑中鉴定出一个4.4 kb的转录本。人类基因定位于6p21.3上两个相距2 Mb的位点。对这两个位点的序列分析表明,着丝粒基因被转录,而端粒位点可能是一个假基因。转录的基因分布在跨越18 kb基因组DNA的22个外显子上。

结论

人类GABAB受体基因的基因组定位、组织表达和功能表明,它是6p21.3上具有基因位点的神经行为障碍的一个重要定位候选基因。此外,基因组结构的描绘现在将使其能够作为抗焦虑、麻醉、抗癫痫和氟西汀治疗试验中药理学遗传学研究的一部分。

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