{"id":974,"date":"2021-02-11T20:47:11","date_gmt":"2021-02-11T12:47:11","guid":{"rendered":"https:\/\/mygenome.asia\/?p=974"},"modified":"2021-02-15T08:57:29","modified_gmt":"2021-02-15T00:57:29","slug":"the-dark-genome-new-sources-of-cancer-proteins","status":"publish","type":"post","link":"https:\/\/mygenome.asia\/zh\/blog\/the-dark-genome-new-sources-of-cancer-proteins\/","title":{"rendered":"The dark genome: new sources of cancer proteins?"},"content":{"rendered":"<p>The human genome is conventionally divided into the \u201ccoding\u201d genome, which generates the ~20,000 annotated human protein coding genes, and the \u201cdark\u201d genome, which does not encode proteins.&nbsp; The dark genome is a vast space, accounting for the ~98.5% of genomic space where repeat elements, enhancers, regulatory sequences, and non-coding RNAs reside.<\/p>\n\n\n\n<p>Historically, a major effort of human genomics has been to define the complement of human protein coding genes, which are then the basis for biomedical discovery and research.&nbsp; Following positional cloning techniques, the 1980s saw the emergence of gene cloning as a major field of research.&nbsp; Major human disease genes such as von Willebrand factor<sup>1<\/sup>&nbsp;and the cystic fibrosis gene&nbsp;<em>CFTR<sup>2,3<\/sup><\/em>&nbsp;were cloned in this way.&nbsp; In the 1990s, high-throughput analyses of complementary DNA (cDNA) provided early insights into human gene structure globally.&nbsp; Methods such as expressed sequence tag (EST) sequencing<sup>4<\/sup>&nbsp;and serial analysis of gene expression (SAGE)<sup>5<\/sup>&nbsp;revolutionized the ability to detect genes and understand exon structure based on spliced mRNAs.&nbsp; Such approaches lead to the belief that there were ~35,000 &#8211; 100,000 human protein coding genes<sup>6,7<\/sup>.<\/p>\n\n\n\n<p>The publication of the Human Genome Project<sup>8<\/sup>&nbsp; (HGP) in 2001 was the culmination of these efforts.&nbsp; Simultaneously, the HGP both dramatically expanded the number of annotated human protein coding genes and dramatically reduced that number from ~100,000 to ~20,000.&nbsp; It has remained at ~20,000 ever since.<\/p>\n\n\n\n<p>With the advent of next generation sequencing methods, Ingolia<em>&nbsp;et al.<\/em>&nbsp;developed a method to sequence genome-wide footprints of ribosome engagement, termed Ribo-seq<sup>9<\/sup>.&nbsp; Beyond confirming the translation of annotated proteins, this method has revolutionized genomic understanding by revealing thousands of genomic sites of ribosome translation in the \u201cdark\u201d genome.&nbsp; The central question, therefore, is how to interpret these data: biological noise? new proteins? a faulty technique?<\/p>\n\n\n\n<p>We have viewed these data as an opportunity to explore the limits of the functional genome.&nbsp; Ribo-seq analyses have nominated thousands of putative sites of translation across the genome<sup>10,11<\/sup>.&nbsp; In our study, published online in Nature Biotechnology<sup>12<\/sup>, we set out to test many of these Ribo-seq ORFs (open reading frames) for function in human cancer cells.&nbsp; We performed three major assays:<\/p>\n\n\n\n<ol class=\"wp-block-list\"><li>Assessment of the ability to translate a stable protein<\/li><li>The ability to change cellular state, as measured by gene expression changes<\/li><li>The requirement of a Ribo-seq ORF for maintenance of cancer cell growth.<\/li><\/ol>\n\n\n\n<p>Surprisingly, of 553 tested Ribo-seq ORFs, we found that ~50% produced a stably-detected protein, ~30% impacted cell gene expression, and ~10% were required for cancer cell viability.<\/p>\n\n\n\n<p>These results suggest that there may be a sizable collection of functional peptides present in human diseases that are not captured by the ~20,000 annotated protein coding genes.&nbsp; While further study is needed to establish whether additional groups of Ribo-seq ORFs will be similarly enriched for potential functions, we are motivated by the possibility that the human genome may harbor a new layer of unexplored biology.&nbsp; Our data provide motivation to continue to search the \u201cdark\u201d genome for new sources of human biology that may be relevant in complex diseases such as cancer.<\/p>\n\n\n\n<p><strong>References<\/strong><\/p>\n\n\n\n<p>1.&nbsp;Ginsburg, D. et al. Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization. Science 228, 1401\u20131406 (1985).<\/p>\n\n\n\n<p>2.&nbsp;Riordan, J. R. et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science 245, 1066\u20131073 (1989).<\/p>\n\n\n\n<p>3.&nbsp;Kerem, B. et al. Identification of the cystic fibrosis gene: genetic analysis. Science vol. 245 1073\u20131080 (1989).<\/p>\n\n\n\n<p>4.&nbsp;Adams, M. D. et al. Complementary DNA sequencing: expressed sequence tags and human genome project. Science 252, 1651\u20131656 (1991).<\/p>\n\n\n\n<p>5.&nbsp;Velculescu, V. E., Zhang, L., Vogelstein, B. &amp; Kinzler, K. W. Serial analysis of gene expression. Science 270, 484\u2013487 (1995).<\/p>\n\n\n\n<p>6.&nbsp;Ewing, B. &amp; Green, P. Analysis of expressed sequence tags indicates 35,000 human genes. Nat. Genet. 25, 232\u2013234 (2000).<\/p>\n\n\n\n<p>7.&nbsp;Liang, F. et al. Gene Index analysis of the human genome estimates approximately 120,000 genes. Nat. Genet. 25, 239\u2013240 (2000).<\/p>\n\n\n\n<p>8.&nbsp;Lander, E. S. et al. Initial sequencing and analysis of the human genome. Nature 409, 860\u2013921 (2001).<\/p>\n\n\n\n<p>9.&nbsp;Ingolia, N. T., Ghaemmaghami, S., Newman, J. R. S. &amp; Weissman, J. S. Genome-wide analysis in vivo of translation with nucleotide resolution using ribosome profiling. Science 324, 218\u2013223 (2009).<\/p>\n\n\n\n<p>10.&nbsp;Ji, Z., Song, R., Regev, A. &amp; Struhl, K. Many lncRNAs, 5\u2019UTRs, and pseudogenes are translated and some are likely to express functional proteins. Elife 4, e08890 (2015).<\/p>\n\n\n\n<p>11.&nbsp;Martinez, T. F. et al. Accurate annotation of human protein-coding small open reading frames. Nat. Chem. Biol. 16, 458\u2013468 (2020).<\/p>\n\n\n\n<p>12.&nbsp;Prensner, J. R., Enache, O. M., Luria, V., Krug, K. &amp; Clauser, K. R. Non-canonical open reading frames encode functional proteins essential for cancer cell survival. Nature Biotechnology (2021).<\/p>","protected":false},"excerpt":{"rendered":"<p>The human genome is conventionally divided into the \u201ccoding\u201d genome, which generates the ~20,000 annotated human protein coding genes, and the \u201cdark\u201d genome, which does not encode proteins.&nbsp; The dark genome is a vast space, accounting for the ~98.5% of genomic space where repeat elements, enhancers, regulatory sequences, and non-coding RNAs reside. Historically, a major [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":975,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[22],"tags":[],"class_list":["post-974","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news_updates"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>The dark genome: new sources of cancer proteins? - MyGenome News_Updates<\/title>\n<meta name=\"description\" content=\"The human genome is conventionally divided into the \u201ccoding\u201d genome, which generates the ~20,000 annotated human protein... - News_Updates\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/mygenome.asia\/zh\/blog\/the-dark-genome-new-sources-of-cancer-proteins\/\" \/>\n<meta property=\"og:locale\" content=\"zh_CN\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"The dark genome: new sources of cancer proteins? 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