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Abstract

Transcription in mammalian cells can be assessed at a genome-wide level, but it has been difficult to reliably determine whether individual transcripts are derived from the plus or minus strands of chromosomes. This distinction can be critical for understanding the relationship between known transcripts (sense) and the complementary antisense transcripts that may regulate them. Here, we describe a technique that can be used to (i) identify the DNA strand of origin for any particular RNA transcript, and (ii) quantify the number of sense and antisense transcripts from expressed genes at a global level. We examined five different human cell types and in each case found evidence for antisense transcripts in 2900 to 6400 human genes. The distribution of antisense transcripts was distinct from that of sense transcripts, was nonrandom across the genome, and differed among cell types. Antisense transcripts thus appear to be a pervasive feature of human cells, which suggests that they are a fundamental component of gene regulation.

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We thank W. Yu for assistance with microarrays. Supported by the Virginia and D. K. Ludwig Fund for Cancer Research and NIH grants CA57345, CA43460, CA62924, and CA121113. Under a licensing agreement between Johns Hopkins University and Genzyme, technologies related to SAGE were licensed to Genzyme for commercial purposes, and B.V., V.E.V., and K.W.K. are entitled to a share of the royalties received by the university from the sales of the licensed technologies. The university and researchers (B.V. and K.W.K.) own Genzyme stock, which is subject to certain restrictions under university policy. The terms of these arrangements are being managed by the university in accordance with its conflict-of-interest policies. There are existing patents for SAGE that have been licensed as disclosed above, and similar patents are likely to be filed for ASSAGE.

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Published In

Science
Volume 322 | Issue 5909
19 December 2008

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Submission history

Received: 26 July 2008
Accepted: 10 November 2008
Published in print: 19 December 2008

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Notes

Supporting Online Material
www.sciencemag.org/cgi/content/full/1163853/DC1
Materials and Methods
Figs. S1 to S13
Tables S1 to S3
References

Authors

Affiliations

Yiping He
Ludwig Center for Cancer Genetics and Therapeutics and Howard Hughes Medical Institute, Johns Hopkins Kimmel Cancer Center, Baltimore, MD 21231, USA.
Bert Vogelstein
Ludwig Center for Cancer Genetics and Therapeutics and Howard Hughes Medical Institute, Johns Hopkins Kimmel Cancer Center, Baltimore, MD 21231, USA.
Victor E. Velculescu
Ludwig Center for Cancer Genetics and Therapeutics and Howard Hughes Medical Institute, Johns Hopkins Kimmel Cancer Center, Baltimore, MD 21231, USA.
Nickolas Papadopoulos* [email protected]
Ludwig Center for Cancer Genetics and Therapeutics and Howard Hughes Medical Institute, Johns Hopkins Kimmel Cancer Center, Baltimore, MD 21231, USA.
Kenneth W. Kinzler
Ludwig Center for Cancer Genetics and Therapeutics and Howard Hughes Medical Institute, Johns Hopkins Kimmel Cancer Center, Baltimore, MD 21231, USA.

Notes

*
To whom correspondence should be addressed. E-mail: [email protected]

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