Nucleic Acids Research Advance Access originally published online on September 9, 2009
Nucleic Acids Research 2009 37(20):6723-6736; doi:10.1093/nar/gkp744
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Nucleic Acids Research, 2009, Vol. 37, No. 20 6723-6736
© The Author(s) 2009. Published by Oxford University Press.
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Gene Regulation, Chromatin and Epigenetics |
Regulation of transcription termination in the nematode Caenorhabditis elegans
Genetics Unit Department of Biochemistry, University of Oxford, Oxford OX1 3QU, UK
*To whom correspondence should be addressed. Tel: 01865 613261; Fax: 01865 613276; Email: andre.furger{at}bioch.ox.ac.uk
Received June 23, 2009. Revised August 20, 2009. Accepted August 24, 2009.
The current predicted mechanisms that describe RNA polymerase II (pol II) transcription termination downstream of protein expressing genes fail to adequately explain, how premature termination is prevented in eukaryotes that possess operon-like structures. Here we address this issue by analysing transcription termination at the end of single protein expressing genes and genes located within operons in the nematode Caenorhabditis elegans. By using a combination of RT-PCR and ChIP analysis we found that pol II generally transcribes up to 1 kb past the poly(A) sites into the 3' flanking regions of the nematode genes before it terminates. We also show that pol II does not terminate after transcription of internal poly(A) sites in operons. We provide experimental evidence that five randomly chosen C. elegans operons are transcribed as polycistronic pre-mRNAs. Furthermore, we show that cis-splicing of the first intron located in downstream positioned genes in these polycistronic pre-mRNAs is critical for their expression and may play a role in preventing premature pol II transcription termination.