...
首页> 外文期刊>Cytogenetic and genome research >Human retroelements may introduce intragenic polyadenylation signals
【24h】

Human retroelements may introduce intragenic polyadenylation signals

机译:人类逆转录因子可能会引入基因内聚腺苷酸化信号

获取原文
获取原文并翻译 | 示例
           

摘要

In the human genome, the insertion of LINE-1 and Alu elements can affect genes by sequence disruption, and by the introduction of elements that modulate the gene's expression. One of the modulating sequences retroelements may contribute is the canonical polyadenylation signal (pA), AATAAA. L1 elements include these within their own sequence and AATAAA sequences are commonly created in the A-rich tails of both SINEs and LINEs. Computational analysis of 34 genes randomly retrieved from the human genome draft sequence reveals an orientation bias, reflected as a lower number of L Is and Alus containing the pA in the same orientation as the gene. Experimental studies of Alu-based pA sequences when placed in pol II or polIII transcripts suggest that the signal is very weak, or often not used at all. Because the pA signal is highly affected by the surrounding sequence, it is likely that the Alu constructs evaluated did not provide the required recognition signals to the polyadenylation machinery. Although the effect of pA signals contributed by Alus is individually weak, the observed reduction of "sense" oriented pA-containing L1 and Alu elements within genes reflects that even a modest influence causes a change in evolutionary pressure, sufficient to create the biased distribution. Copyright (c) 2005 S. Karger AG, Basel.
机译:在人类基因组中,LINE-1和Alu元素的插入可通过序列破坏和引入可调节基因表达的元素来影响基因。逆转录元件可能起作用的调节序列之一是规范的聚腺苷酸化信号(pA),AATAAA。 L1元素将这些元素包含在它们自己的序列中,并且AATAAA序列通常在SINE和LINE的富含A的尾部中创建。对从人类基因组草图序列中随机检索到的34个基因的计算分析揭示了方向偏差,反映为包含与该基因相同方向的pA的L Is和Alus数量减少。基于Alu的pA序列置于pol II或polIII转录本中的实验研究表明,该信号非常微弱,或者通常根本不使用。由于pA信号受周围序列的影响很大,所评估的Alu构建体可能未向聚腺苷酸化机制提供所需的识别信号。尽管由Alus贡献的pA信号的作用个别较弱,但观察到的基因内“有义”取向的包含pA的L1和Alu元素的减少反映出,即使适度的影响也会导致进化压力发生变化,足以产生偏差分布。版权所有(c)2005 S.Karger AG,巴塞尔。

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