Pseudogenes: Pseudo-functional or key regulators in health and disease?

被引:302
作者
Pink, Ryan Charles [1 ]
Wicks, Kate [1 ]
Caley, Daniel Paul [1 ]
Punch, Emma Kathleen [1 ]
Jacobs, Laura [1 ]
Carter, David Raul Francisco [1 ]
机构
[1] Oxford Brookes Univ, Sch Life Sci, Oxford OX3 0BP, England
关键词
pseudogenes; functional; noncoding RNA; transcription; RNA; MESSENGER-RNA STABILITY; HOMOLOGOUS CODING GENE; GENOME TILING ARRAYS; PROCESSED PSEUDOGENES; DROSOPHILA-MELANOGASTER; MOLECULAR EVOLUTION; BACTERIAL GENOMES; NONCODING RNAS; MOUSE OOCYTES; TUMOR-CELLS;
D O I
10.1261/rna.2658311
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pseudogenes have long been labeled as "junk'' DNA, failed copies of genes that arise during the evolution of genomes. However, recent results are challenging this moniker; indeed, some pseudogenes appear to harbor the potential to regulate their protein-coding cousins. Far from being silent relics, many pseudogenes are transcribed into RNA, some exhibiting a tissue-specific pattern of activation. Pseudogene transcripts can be processed into short interfering RNAs that regulate coding genes through the RNAi pathway. In another remarkable discovery, it has been shown that pseudogenes are capable of regulating tumor suppressors and oncogenes by acting as microRNA decoys. The finding that pseudogenes are often deregulated during cancer progression warrants further investigation into the true extent of pseudogene function. In this review, we describe the ways in which pseudogenes exert their effect on coding genes and explore the role of pseudogenes in the increasingly complex web of noncoding RNA that contributes to normal cellular regulation.
引用
收藏
页码:792 / 798
页数:7
相关论文
共 82 条
[1]   Subtle variations in Pten dose determine cancer susceptibility [J].
Alimonti, Andrea ;
Carracedo, Arkaitz ;
Clohessy, John G. ;
Trotman, Lloyd C. ;
Nardella, Caterina ;
Egia, Ainara ;
Salmena, Leonardo ;
Sampieri, Katia ;
Haveman, William J. ;
Brogi, Edi ;
Richardson, Andrea L. ;
Zhang, Jiangwen ;
Pandolfi, Pier Paolo .
NATURE GENETICS, 2010, 42 (05) :454-U136
[2]   Pseudogenes: Are they "Junk" or functional DNA? [J].
Balakirev, ES ;
Ayala, FJ .
ANNUAL REVIEW OF GENETICS, 2003, 37 :123-151
[3]  
Balakirev ES, 2003, GENETICS, V164, P533
[4]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[5]   Processed pseudogenes, processed genes, and spontaneous mutations in the Arabidopsis genome [J].
Benovoy, David ;
Drouin, Guy .
JOURNAL OF MOLECULAR EVOLUTION, 2006, 62 (05) :511-522
[6]   Global identification of human transcribed sequences with genome tiling arrays [J].
Bertone, P ;
Stolc, V ;
Royce, TE ;
Rozowsky, JS ;
Urban, AE ;
Zhu, XW ;
Rinn, JL ;
Tongprasit, W ;
Samanta, M ;
Weissman, S ;
Gerstein, M ;
Snyder, M .
SCIENCE, 2004, 306 (5705) :2242-2246
[7]  
BRISTOW J, 1993, J BIOL CHEM, V268, P12919
[8]   Transcriptional regulation of human insulin receptor gene by the high-mobility group protein HMGI(Y) [J].
Brunetti, A ;
Manfioletti, G ;
Chiefari, E ;
Goldfine, ID ;
Foti, D .
FASEB JOURNAL, 2001, 15 (02) :492-500
[9]   Long Noncoding RNAs, Chromatin, and Development [J].
Caley, Daniel P. ;
Pink, Ryan C. ;
Trujillano, Daniel ;
Carter, David R. F. .
THESCIENTIFICWORLDJOURNAL, 2010, 10 :90-102
[10]   Transcriptional maps of 10 human chromosomes at 5-nucleotide resolution [J].
Cheng, J ;
Kapranov, P ;
Drenkow, J ;
Dike, S ;
Brubaker, S ;
Patel, S ;
Long, J ;
Stern, D ;
Tammana, H ;
Helt, G ;
Sementchenko, V ;
Piccolboni, A ;
Bekiranov, S ;
Bailey, DK ;
Ganesh, M ;
Ghosh, S ;
Bell, I ;
Gerhard, DS ;
Gingeras, TR .
SCIENCE, 2005, 308 (5725) :1149-1154