Suppr超能文献

对随机选取的粗壮真核游仆虫大核基因进行测序,结果支持了较高频率的 +1 移码翻译现象。

Sequencing of random Euplotes crassus macronuclear genes supports a high frequency of +1 translational frameshifting.

作者信息

Klobutcher Lawrence A

机构信息

Department of Molecular, Microbial and Structural Biology, University of Connecticut Health Center, Farmington, CT 06032, USA.

出版信息

Eukaryot Cell. 2005 Dec;4(12):2098-105. doi: 10.1128/EC.4.12.2098-2105.2005.

Abstract

Programmed translational frameshifts have been identified in genes from a broad range of organisms, but typically only a very few genes in a given organism require a frameshift for expression. In contrast, a recent analysis of gene sequences available in GenBank from ciliates in the genus Euplotes indicated that >5% required one or more +1 translational frameshifts to produce their predicted protein products. However, this sample of genes was nonrandom, biased, and derived from multiple Euplotes species. To test whether there truly is an abundance of frameshift genes in Euplotes, and to more accurately assess their frequency, we sequenced a random sample of 25 cloned genes/macronuclear DNA molecules from Euplotes crassus. Three new candidate +1 frameshift genes were identified in the sample that encode a membrane occupation and recognition nexus (MORN) repeat protein, a C(2)H(2)-type zinc finger protein, and a Ser/Thr protein kinase. Reverse transcription-PCR analyses indicate that all three genes are expressed in vegetatively proliferating cells and that the mRNAs retain the requirement of a frameshift. Although the sample of sequenced genes is relatively small, the results indicate that the frequency of genes requiring frameshifts in E. crassus is between 3.7% and 31.7% (at a 95% confidence interval). The current and past data also indicate that frameshift sites are found predominantly in genes that likely encode nonabundant proteins in the cell.

摘要

在广泛的生物体基因中都已鉴定出程序性翻译移码现象,但在特定生物体中,通常只有极少数基因的表达需要移码。相比之下,最近对GenBank中纤毛虫纲游仆虫属基因序列的分析表明,超过5%的基因需要一个或多个+1翻译移码来产生其预测的蛋白质产物。然而,这个基因样本是非随机的、有偏差的,并且来自多个游仆虫物种。为了测试游仆虫中是否真的存在大量移码基因,并更准确地评估它们的频率,我们对来自粗壮游仆虫的25个克隆基因/大核DNA分子进行了随机测序。在样本中鉴定出三个新的候选+1移码基因,它们分别编码一个膜占据与识别连接(MORN)重复蛋白、一个C(2)H(2)型锌指蛋白和一个丝氨酸/苏氨酸蛋白激酶。逆转录PCR分析表明,这三个基因在营养增殖细胞中均有表达,并且mRNA仍然需要移码。尽管测序的基因样本相对较小,但结果表明,粗壮游仆虫中需要移码的基因频率在3.7%至31.7%之间(95%置信区间)。目前和过去的数据还表明,移码位点主要存在于可能编码细胞中丰度较低蛋白质的基因中。

相似文献

引用本文的文献

2
Nontriplet feature of genetic code in ciliates is a result of neutral evolution.纤毛虫遗传密码的非同三联体特征是中性进化的结果。
Proc Natl Acad Sci U S A. 2023 May 30;120(22):e2221683120. doi: 10.1073/pnas.2221683120. Epub 2023 May 22.

本文引用的文献

6
WebLogo: a sequence logo generator.WebLogo:一个序列图生成器。
Genome Res. 2004 Jun;14(6):1188-90. doi: 10.1101/gr.849004.
7
Reprogrammed genetic decoding in cellular gene expression.细胞基因表达中的重编程基因解码
Mol Cell. 2004 Jan 30;13(2):157-68. doi: 10.1016/s1097-2765(04)00031-0.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验