Antisense RNAs during early vertebrate development are divided in groups with distinct features

被引:11
作者
Pillay, Sanjana [1 ]
Takahashi, Hazuki [2 ]
Carninci, Piero [2 ,3 ]
Kanhere, Aditi [4 ,5 ]
机构
[1] Mt Sinai Sch Med, Dept Cell Dev & Regenerat Biol, New York, NY 10029 USA
[2] RIKEN Ctr Integrat Med Sci, Lab Transcriptome Technol, Yokohama, Kanagawa 2300045, Japan
[3] Fdn Human Technopole, I-20157 Milan, Italy
[4] Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool L69 3GE, Merseyside, England
[5] Univ Liverpool, Inst Syst Mol & Integrat Biol, Dept Mol Physiol & Cell Signaling, Liverpool L69 3BX, Merseyside, England
关键词
LONG NONCODING RNAS; GENE-EXPRESSION; MESSENGER-RNA; SEQ EXPERIMENTS; DATA-RETRIEVAL; CHROMATIN; TRANSCRIPTION; LOCALIZATION; SENSE; PLURIPOTENCY;
D O I
10.1101/gr.262964.120
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
Long noncoding RNAs or lncRNAs are a class of non-protein-coding RNAs that are >200 nt in length. Almost 50% of lncRNAs during zebrafish development are transcribed in an antisense direction to a protein-coding gene. However, the role of these natural antisense transcripts (NATs) during development remains enigmatic. To understand NATs in early vertebrate development, we took a computational biology approach and analyzed existing as well as novel data sets. Our analysis indicates that zebrafish NATs can be divided into two major classes based on their coexpression patterns with respect to the overlapping protein-coding genes. Group 1 NATs have characteristics similar to maternally deposited RNAs in that their levels decrease as development progresses. Group 1 NAT levels are negatively correlated with that of overlapping sense-strand protein-coding genes. Conversely, Group 2 NATs are coexpressed with overlapping protein-coding genes. In contrast to Group 1, which is enriched in genes involved in developmental pathways, Group 2 protein-coding genes are enriched in housekeeping functions. Group 1 NATs also show larger overlap and higher complementarity with the sense strand mRNAs compared to other NATs. In addition, our transcriptomics data, quantifying RNA levels from cytoplasmic and nuclear compartments, indicates that Group 1 NATs are more abundant in the cytosol. Based on their expression pattern, cytosolic nature, and their higher complementarity to the overlapping developmental mRNAs, we speculate that Group 1 NATs function post-transcriptionally to silence spurious expression of developmental genes.
引用
收藏
页码:995 / 1010
页数:16
相关论文
共 88 条
[1]   Polycomb complexes in stem cells and embryonic development [J].
Aloia, Luigi ;
Di Stefano, Bruno ;
Di Croce, Luciano .
DEVELOPMENT, 2013, 140 (12) :2525-2534
[2]   The landscape of antisense gene expression in human cancers [J].
Balbin, O. Alejandro ;
Malik, Rohit ;
Dhanasekaran, Saravana M. ;
Prensner, John R. ;
Cao, Xuhong ;
Wu, Yi-Mi ;
Robinson, Dan ;
Wang, Rui ;
Chen, Guoan ;
Beer, David G. ;
Nesvizhskii, Alexey I. ;
Chinnaiyan, Arul M. .
GENOME RESEARCH, 2015, 25 (07) :1068-1079
[3]   A natural antisense transcript regulates Zeb2/Sip1 gene expression during Snail1-induced epithelial-mesenchymal transition [J].
Beltran, Manuel ;
Puig, Isabel ;
Pena, Cristina ;
Miguel Garcia, Jose ;
Belen Alvarez, Ana ;
Pena, Raul ;
Bonilla, Felix ;
Garcia de Herreros, Antonio .
GENES & DEVELOPMENT, 2008, 22 (06) :756-769
[4]   A Novel H19 Antisense RNA Overexpressed in Breast Cancer Contributes to Paternal IGF2 Expression [J].
Berteaux, Nathalie ;
Aptel, Nathalie ;
Cathala, Guy ;
Genton, Celine ;
Coll, Jean ;
Daccache, Anthony ;
Spruyt, Nathalie ;
Hondermarck, Hubert ;
Dugimont, Thierry ;
Curgy, Jean-Jacques ;
Forne, Thierry ;
Adriaenssens, Eric .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (22) :6731-6745
[5]   Histone Lysine Methylation Dynamics: Establishment, Regulation, and Biological Impact [J].
Black, Joshua C. ;
Van Rechem, Capucine ;
Whetstine, Johnathan R. .
MOLECULAR CELL, 2012, 48 (04) :491-507
[6]   Dynamics of enhancer chromatin signatures mark the transition from pluripotency to cell specification during embryogenesis [J].
Bogdanovic, Ozren ;
Fernandez-Minan, Ana ;
Tena, Juan J. ;
de la Calle-Mustienes, Elisa ;
Hidalgo, Carmen ;
van Kruysbergen, Ila ;
van Heeringen, Simon J. ;
Veenstra, Gert Jan C. ;
Luis Gomez-Skarmeta, Jose .
GENOME RESEARCH, 2012, 22 (10) :2043-2053
[7]   Trimmomatic: a flexible trimmer for Illumina sequence data [J].
Bolger, Anthony M. ;
Lohse, Marc ;
Usadel, Bjoern .
BIOINFORMATICS, 2014, 30 (15) :2114-2120
[8]   Isolation and characterization of runxa and runxb, zebrafish members of the runt family of transcriptional regulators [J].
Burns, CE ;
DeBlasio, T ;
Zhou, Y ;
Zhang, J ;
Zon, L ;
Nimer, SD .
EXPERIMENTAL HEMATOLOGY, 2002, 30 (12) :1381-1389
[9]   Localization and abundance analysis of human IncRNAs at single-cell and single-molecule resolution [J].
Cabili, Moran N. ;
Dunagin, Margaret C. ;
McClanahan, Patrick D. ;
Biaesch, Andrew ;
Padovan-Merhar, Olivia ;
Regev, Aviv ;
Rinn, John L. ;
Raj, Arjun .
GENOME BIOLOGY, 2015, 16
[10]   High-efficiency full-length cDNA cloning by biotinylated CAP trapper [J].
Carninci, P ;
Kvam, C ;
Kitamura, A ;
Ohsumi, T ;
Okazaki, Y ;
Itoh, M ;
Kamiya, M ;
Shibata, K ;
Sasaki, N ;
Izawa, M ;
Muramatsu, M ;
Hayashizaki, Y ;
Schneider, C .
GENOMICS, 1996, 37 (03) :327-336