...
首页> 外文期刊>Human Molecular Genetics >Transcriptional activity of multiple copies of a subtelomerically located olfactory receptor gene that is polymorphic in number and location.
【24h】

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

机译:在数量和位置上是多态的亚端粒型嗅觉受体基因的多个拷贝的转录活性。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

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.
机译:我们在这里报告位于一个亚端的嗅觉受体(OR)基因OR-A的多个副本的转录活性。由于最近的复制事件,OR-A的拷贝数和染色体位置在人类之间都不同。对来自22个个体的12个染色体末端的180个拷贝的该基因进行序列分析,结果表明,除一个拷贝外,所有该基因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。我们使用RT-PCR扩增技术,利用基于计算预测的基因结构设计的引物,在嗅觉上皮和睾丸组织中检测到OR-A的转录。在两个组织中均发现了两种交替剪接的转录本形式,一种编码带有延伸的N端的同种型。在睾丸中也观察到源自第二启动子的第三转录物。预测所有转录物中的起始蛋氨酸位于上游外显子,而不是主要编码外显子,这是大多数其他OR基因的典型现象。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。我们的研究结果证实了在易重排的亚端粒区域可能产生OR多样性的想法,并表明亚端粒区域中的多态性可能导致OR基因表达谱中的个体差异。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号