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Nucleic Acids Research 2006 34(12):3465-3475; doi:10.1093/nar/gkl473
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Published online 18 July 2006

© 2006 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (
http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commerical use, distribution, and reproduction in any medium, provided the original work is properly cited.


Article

Genome-wide in silico identification and analysis of cis natural antisense transcripts (cis-NATs) in ten species

Yong Zhang, X. Shirley Liu1, Qing-Rong Liu2 and Liping Wei*

Center for Bioinformatics, National Laboratory of Protein Engineering and Plant Genetic Engineering, College of Life Sciences, Peking University Beijing 100871, P. R. China 1 Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Harvard School of Public Health 44 Binney Street, M1B22, Boston, MA 02115, USA 2 Molecular Neurobiology Branch, National Institute on Drug Abuse-Intramural Research Program (NIDA-IRP), NIH, Department of Health and Human Services (DHHS) Box 5180, Baltimore, MD 21224, USA

*To whom correspondence should be addressed. Tel: +86 10 6276 4970; Fax: +86 10 6275 2438; Email: weilp{at}mail.cbi.pku.edu.cn

Received April 4, 2006. Revised May 10, 2006. Accepted June 21, 2006.

We developed a fast, integrative pipeline to identify cis natural antisense transcripts (cis-NATs) at genome scale. The pipeline mapped mRNAs and ESTs in UniGene to genome sequences in GoldenPath to find overlapping transcripts and combining information from coding sequence, poly(A) signal, poly(A) tail and splicing sites to deduce transcription orientation. We identified cis-NATs in 10 eukaryotic species, including 7830 candidate sense–antisense (SA) genes in 3915 SA pairs in human. The abundance of SA genes is remarkably low in worm and does not seem to be caused by the prevalence of operons. Hundreds of SA pairs are conserved across different species, even maintaining the same overlapping patterns. The convergent SA class is prevalent in fly, worm and sea squirt, but not in human or mouse as reported previously. The percentage of SA genes among imprinted genes in human and mouse is 24–47%, a range between the two previous reports. There is significant shortage of SA genes on Chromosome X in human and mouse but not in fly or worm, supporting X-inactivation in mammals as a possible cause. SA genes are over-represented in the catalytic activities and basic metabolism functions. All candidate cis-NATs can be downloaded from http://nats.cbi.pku.edu.cn/download/.


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