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一个位于亚端粒区域的嗅觉受体基因多拷贝的转录活性,该基因在数量和位置上具有多态性。

Transcriptional activity of multiple copies of a subtelomerically located olfactory receptor gene that is polymorphic in number and location.

作者信息

Linardopoulou E, Mefford H C, Nguyen O, Friedman C, van den Engh G, Farwell D G, Coltrera M, Trask B J

机构信息

Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

出版信息

Hum Mol Genet. 2001 Oct 1;10(21):2373-83. doi: 10.1093/hmg/10.21.2373.

Abstract

We report here on the transcriptional activity of multiple copies of a subtelomerically located olfactory receptor (OR) gene, OR-A. Due to recent duplication events, both the copy number and chromosomal location of OR-A vary among humans. Sequence analyses of 180 copies of this gene, derived from 12 chromosome ends in 22 individuals, show that the main coding exon of all but one copy is an intact open reading frame with 0-5 predicted amino acid differences. We detected transcription of OR-A in both olfactory epithelium and testis tissue using RT-PCR amplification with primers designed on the basis of a computationally predicted gene structure. Two alternatively spliced forms of transcripts, one encoding an isoform with an extended N-terminus, were found in both tissues. A third transcript, derived from a second promoter, was also observed in testes. The start methionine is predicted in all transcripts to lie in an upstream exon rather than the main coding exon, as is typical for most other OR genes. By examining sequence variants among transcripts, we show that transcription of this gene occurs at multiple chromosomal locations. Our results lend credence to the idea that OR diversity could be generated in rearrangement-prone subtelomeric regions and show that polymorphism in subtelomeric regions could lead to individual-to-individual variation in the expressed repertoire of OR genes.

摘要

我们在此报告位于亚端粒区域的嗅觉受体(OR)基因OR - A多个拷贝的转录活性。由于近期的复制事件,OR - A的拷贝数和染色体定位在人类中存在差异。对来自22个个体12个染色体末端的该基因180个拷贝进行序列分析表明,除一个拷贝外,所有拷贝的主要编码外显子都是完整的开放阅读框,预测的氨基酸差异为0 - 5个。我们使用基于计算预测的基因结构设计的引物,通过RT - PCR扩增在嗅觉上皮组织和睾丸组织中检测到了OR - A的转录。在这两种组织中均发现了两种选择性剪接的转录本形式,其中一种编码具有延长N末端的异构体。在睾丸中还观察到了源自第二个启动子的第三种转录本。与大多数其他OR基因不同,所有转录本中的起始甲硫氨酸预计位于上游外显子而非主要编码外显子中。通过检查转录本之间的序列变异,我们表明该基因的转录发生在多个染色体位置。我们的结果支持了这样一种观点,即OR多样性可能在易于发生重排的亚端粒区域产生,并且表明亚端粒区域的多态性可能导致个体间OR基因表达谱的差异。

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