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Mechanisms of antisense transcription initiation from the 3' end of the GAL10 coding sequence in vivo. | LitMetric

AI Article Synopsis

  • Antisense transcripts play a crucial role in gene expression regulation, but the initiation process of antisense transcription is still not well understood.
  • Recent findings suggest that RNA polymerase II is involved in this initiation, yet the specific targeting mechanisms remain unclear.
  • Our analysis showed that RNA polymerase II is directed to the antisense initiation site of the GAL10 gene by the Reb1p activator and certain transcription factors, revealing distinct regulatory pathways for sense and antisense transcription despite their association with the same gene.

Article Abstract

In spite of the important regulatory functions of antisense transcripts in gene expression, it remains unknown how antisense transcription is initiated. Recent studies implicated RNA polymerase II in initiation of antisense transcription. However, how RNA polymerase II is targeted to initiate antisense transcription has not been elucidated. Here, we have analyzed the association of RNA polymerase II with the antisense initiation site at the 3' end of the GAL10 coding sequence in dextrose-containing growth medium that induces antisense transcription. We find that RNA polymerase II is targeted to the antisense initiation site at GAL10 by Reb1p activator as well as general transcription factors (e.g., TFIID, TFIIB, and Mediator) for antisense transcription initiation. Intriguingly, while GAL10 antisense transcription is dependent on TFIID, its sense transcription does not require TFIID. Further, the Gal4p activator that promotes GAL10 sense transcription is dispensable for antisense transcription. Moreover, the proteasome that facilitates GAL10 sense transcription does not control its antisense transcription. Taken together, our results reveal that GAL10 sense and antisense transcriptions are regulated differently and shed much light on the mechanisms of antisense transcription initiation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753873PMC
http://dx.doi.org/10.1128/MCB.01715-12DOI Listing

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