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Yiping He,Bert Vogelstein,Victor E. Velculescu,Nickolas Papadopoulos,*Kenneth W. Kinzler
Transcription in mammalian cells can be assessed at a genome-widelevel, but it has been difficult to reliably determine whetherindividual transcripts are derived from the plus or minus strandsof chromosomes. This distinction can be critical for understandingthe relationship between known transcripts (sense) and the complementaryantisense transcripts that may regulate them. Here, we describea technique that can be used to (i) identify the DNA strandof origin for any particular RNA transcript, and (ii) quantifythe number of sense and antisense transcripts from expressedgenes at a global level. We examined five different human celltypes and in each case found evidence for antisense transcriptsin 2900 to 6400 human genes. The distribution of antisense transcriptswas distinct from that of sense transcripts, was nonrandom acrossthe genome, and differed among cell types. Antisense transcriptsthus appear to be a pervasive feature of human cells, whichsuggests that they are a fundamental component of gene regulation.
Ludwig Center for Cancer Genetics and Therapeutics and Howard Hughes Medical Institute, Johns Hopkins Kimmel Cancer Center, Baltimore, MD 21231, USA.
* To whom correspondence should be addressed. E-mail: npapado1{at}jhmi.edu
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[DOI: 10.1126/science.1168805] |Summary »|Full Text »|PDF »
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