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荧光假单胞菌 Pf0-1 中非注释蛋白编码基因的蛋白质组学检测。

Proteomic detection of non-annotated protein-coding genes in Pseudomonas fluorescens Pf0-1.

机构信息

Center for Adaptation Genetics and Drug Resistance and Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts, United States of America.

出版信息

PLoS One. 2009 Dec 24;4(12):e8455. doi: 10.1371/journal.pone.0008455.

Abstract

Genome sequences are annotated by computational prediction of coding sequences, followed by similarity searches such as BLAST, which provide a layer of possible functional information. While the existence of processes such as alternative splicing complicates matters for eukaryote genomes, the view of bacterial genomes as a linear series of closely spaced genes leads to the assumption that computational annotations that predict such arrangements completely describe the coding capacity of bacterial genomes. We undertook a proteomic study to identify proteins expressed by Pseudomonas fluorescens Pf0-1 from genes that were not predicted during the genome annotation. Mapping peptides to the Pf0-1 genome sequence identified sixteen non-annotated protein-coding regions, of which nine were antisense to predicted genes, six were intergenic, and one read in the same direction as an annotated gene but in a different frame. The expression of all but one of the newly discovered genes was verified by RT-PCR. Few clues as to the function of the new genes were gleaned from informatic analyses, but potential orthologs in other Pseudomonas genomes were identified for eight of the new genes. The 16 newly identified genes improve the quality of the Pf0-1 genome annotation, and the detection of antisense protein-coding genes indicates the under-appreciated complexity of bacterial genome organization.

摘要

基因组序列通过计算预测编码序列进行注释,然后进行相似性搜索,如 BLAST,这提供了一层可能的功能信息。虽然像可变剪接这样的过程使真核生物基因组的情况变得复杂,但细菌基因组被视为一系列紧密间隔的基因,这导致人们假设计算预测的这种排列完全描述了细菌基因组的编码能力。我们进行了一项蛋白质组学研究,以鉴定来自 Pf0-1 荧光假单胞菌中未在基因组注释过程中预测到的基因表达的蛋白质。将肽映射到 Pf0-1 基因组序列中,确定了十六个未注释的蛋白质编码区,其中九个是与预测基因反义的,六个是基因间的,一个在与注释基因相同的方向但在不同的框架中读取。除了一个新发现的基因外,所有基因的表达都通过 RT-PCR 得到了验证。从信息学分析中几乎没有获得关于新基因功能的线索,但在其他假单胞菌基因组中为其中 8 个新基因鉴定到了潜在的同源基因。这 16 个新鉴定的基因提高了 Pf0-1 基因组注释的质量,并且检测到反义蛋白质编码基因表明了细菌基因组组织的复杂性被低估了。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df42/2794547/b73fd003f911/pone.0008455.g001.jpg

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