Mira Alex, Pushker Ravindra
Mol Biol Evol. 2005 Nov;22(11):2135-8. doi: 10.1093/molbev/msi209. Epub 2005 Jul 13.
Pseudogenes are nonfunctional DNA sequences that can accumulate in the genomes of some bacterial species, especially those undergoing processes like niche change, host specialization, or weak selection strength. They may last for long evolutionary periods, opening the question of how the genome prevents expression of these degenerated or disrupted genes that would presumably give rise to malfunctioning proteins. We have investigated ribosomal binding strength at Shine-Dalgarno sequences and the prevalence of sigma70 promoter regions in pseudogenes across bacteria. It is reported that the RNA polymerase-binding sites and more strongly the ribosome-binding regions of pseudogenes are highly degraded, suggesting that transcription and translation are impaired in nonfunctional open reading frames. This would reduce the metabolic investment on faulty proteins because although pseudogenes can persist for long time periods, they would be effectively silenced. It is unclear whether mutation accumulation on regulatory regions is neutral or whether it is accelerated by selection.
假基因是无功能的DNA序列,可在一些细菌物种的基因组中积累,尤其是那些经历生态位变化、宿主专一化或弱选择强度等过程的细菌。它们可能会持续很长的进化时期,这就引发了一个问题:基因组是如何阻止这些可能会产生功能异常蛋白质的退化或破坏基因的表达的。我们研究了细菌中假基因的Shine-Dalgarno序列处的核糖体结合强度以及sigma70启动子区域的普遍性。据报道,假基因的RNA聚合酶结合位点,尤其是核糖体结合区域高度降解,这表明无功能的开放阅读框中的转录和翻译受到损害。这将减少对错误蛋白质的代谢投入,因为尽管假基因可以长期存在,但它们会被有效沉默。目前尚不清楚调控区域的突变积累是中性的,还是会因选择而加速。