Zemsky Jennifer, Mandecki Wlodek, Goldman Emanuel
Department of Microbiology & Molecular Genetics, New Jersey Medical School, University of Medicine & Dentistry of New Jersey, Newark 07103, USA.
Gene Expr. 2002;10(3):109-14.
An unusual peptide-encoding sequence, called H10, and several derivatives of this sequence were previously isolated from a random peptide library screened by phage display during drug discovery protocols. The H10 family of sequences had the unusual property of being expressed despite the absence of an open reading frame. When these sequences were fused to a reporter lacZ gene in all three frames, beta-galactosidase was expressed not only from the parental non-open reading frame, consistent with the original isolations, but also from the frame -1 to the parental. This unexpected translation in a second reading frame could result from either a recoding event or from an internal translation initiation event. In order to elucidate which type of event, a genetic approach was selected to eliminate a potential downstream initiator site within the H10 sequence. This report provides strong evidence that translation in the -1 frame in this family of sequences is indeed originating from a downstream translation initiation event. Unexpectedly, the mutation eliminating the downstream initiation event in the -1 frame simultaneously elevated expression in the original non-open reading frame.
一种名为H10的不寻常的肽编码序列及其该序列的几种衍生物,先前是在药物发现方案中通过噬菌体展示筛选的随机肽库中分离得到的。H10序列家族具有一种不寻常的特性,即尽管没有开放阅读框也能表达。当这些序列在所有三个阅读框中与报告基因lacZ融合时,β-半乳糖苷酶不仅从亲本非开放阅读框中表达,这与最初的分离结果一致,而且还从亲本的-1阅读框中表达。在第二个阅读框中的这种意外翻译可能是由重编码事件或内部翻译起始事件引起的。为了阐明是哪种类型的事件,选择了一种遗传学方法来消除H10序列内潜在的下游起始位点。本报告提供了有力证据,证明该序列家族中-1阅读框的翻译确实源自下游翻译起始事件。出乎意料的是,消除-1阅读框中下游起始事件的突变同时提高了原始非开放阅读框中的表达。