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小开放阅读框:一种验证的比较遗传学方法。

Small open reading frames: a comparative genetics approach to validation.

机构信息

Department of Genetics and Genomic Sciences and Mindich Child Health and Development Institute, Icahn School of Medicine at Mount, Hess Center for Science and Medicine, 1470 Madison Avenue, New York, NY, 10029, USA.

Present Address: Committee On Genetics, Genomics, and Systems Biology, The University of Chicago, Chicago, IL, USA.

出版信息

BMC Genomics. 2023 May 1;24(1):226. doi: 10.1186/s12864-023-09311-7.

Abstract

Open reading frames (ORFs) with fewer than 100 codons are generally not annotated in genomes, although bona fide genes of that size are known. Newer biochemical studies have suggested that thousands of small protein-coding ORFs (smORFs) may exist in the human genome, but the true number and the biological significance of the micropeptides they encode remain uncertain. Here, we used a comparative genomics approach to identify high-confidence smORFs that are likely protein-coding. We identified 3,326 high-confidence smORFs using constraint within human populations and evolutionary conservation as additional lines of evidence. Next, we validated that, as a group, our high-confidence smORFs are conserved at the amino-acid level rather than merely residing in highly conserved non-coding regions. Finally, we found that high-confidence smORFs are enriched among disease-associated variants from GWAS. Overall, our results highlight that smORF-encoded peptides likely have important functional roles in human disease.

摘要

开放阅读框(ORFs)少于 100 个密码子通常不会在基因组中注释,尽管已知有大小相当的真实基因。新的生化研究表明,人类基因组中可能存在数千个小的蛋白质编码 ORFs(smORFs),但它们编码的微肽的确切数量和生物学意义仍不确定。在这里,我们使用比较基因组学方法来鉴定可能编码蛋白质的高可信度 smORFs。我们使用人类群体内的约束和进化保守性作为额外的证据,确定了 3326 个高可信度的 smORFs。接下来,我们验证了作为一个整体,我们的高可信度 smORFs 在氨基酸水平上是保守的,而不仅仅是存在于高度保守的非编码区域。最后,我们发现高可信度 smORFs 在来自 GWAS 的疾病相关变异中富集。总的来说,我们的结果强调了 smORF 编码的肽可能在人类疾病中具有重要的功能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d73/10152738/afe5dd3294e3/12864_2023_9311_Fig1_HTML.jpg

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