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RNA Pol II subunit Rpb7 promotes centromeric transcription and RNAi-directed chromatin silencing
Södertörns högskola, Institutionen för livsvetenskaper. Karolinska Institutet.
University of Edinburgh, Edinburgh, UK.
Karolinska Institutet.
Södertörns högskola, Institutionen för livsvetenskaper. Karolinska Institutet.
Vise andre og tillknytning
2005 (engelsk)Inngår i: Genes & Development, ISSN 0890-9369, E-ISSN 1549-5477, Vol. 19, nr 19, s. 2301-2306Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Fission yeast centromeric repeats are transcribed into small interfering RNA (siRNA) precursors (pre-siRNAs), which are processed by Dicer to direct heterochromatin formation. Recently, Rpb1 and Rpb2 subunits of RNA polymerase II (RNA Pol II) were shown to mediate RNA interference (RNAi)-directed chromatin modification but did not affect pre-siRNA levels. Here we show that another Pol II subunit, Rpb7 has a specific role in presiRNA transcription. We define a centromeric presiRNA promoter from which initiation is exquisitely sensitive to the rpb7-G150D mutation. In contrast to other Pol II subunits, Rpb7 promotes pre-siRNA transcription required for RNAi-directed chromatin silencing.

sted, utgiver, år, opplag, sider
2005. Vol. 19, nr 19, s. 2301-2306
HSV kategori
Identifikatorer
URN: urn:nbn:se:sh:diva-14442DOI: 10.1101/gad.344205ISI: 000232433000008PubMedID: 16204182Scopus ID: 2-s2.0-25844480848OAI: oai:DiVA.org:sh-14442DiVA, id: diva2:487425
Tilgjengelig fra: 2012-01-31 Laget: 2011-12-23 Sist oppdatert: 2017-07-19bibliografisk kontrollert
Inngår i avhandling
1. Characterization of RNA polymerase II subunit Rpb7 in silencing and transcription
Åpne denne publikasjonen i ny fane eller vindu >>Characterization of RNA polymerase II subunit Rpb7 in silencing and transcription
2009 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

The DNA in eukaryotes is arranged in fibres of chromatin. The chromatin may be more or less compacted and the degree of condensation of the chromatin affects the accessibility of the DNA. The accessibility of the DNA, in turn, affects transcription and gene regulation. Genes within inaccessible DNA are commonly repressed whereasgenes within accessible DNA are active and expressed. This thesis concerns the interplay between chromatin and transcription with focus on the function of the RNA polymerase II (pol II) subunit Rpb7. We have demonstrated that processing of centromeric transcripts by the ribonuclease III family protein Dcr1 is required for heterochromatin formation at the centromeres of Schizosaccharomyces pombe. A point mutation in the pol II subunit Rpb7 caused a specific defect in centromeric heterochromatin formation. We have shown i) that the centromeric transcripts that accumulate in dcr1delta cells are products of pol II, ii) the rpbG150D mutation is deficient in recognition and/or initiation of transcription from the centromeric promoter. Transcription by pol II within the centromeres was surprising since insertion of marker genes within these loci normally results in repression of pol II transcription. Here, paradoxically, pol II transcription was required for the construction of the inaccessible heterochromatin structure. Our analysis of sRNA in S. pombe revealed that most centromeric siRNA are originating from two clusters, which are repeated several times within the centromeres. This lead us to propose a model in which centromeric transcripts fold into double stranded structures that are processed by Dcr1. The resulting siRNAs may contribute with the starting signal for the RNAi feedback loop required for heterochromatin formation at the centromeres. Finally, we demonstrate that the genome-wide association of Rpb7 is nearly identical to that of the core pol II subunit Rpb2, indicating a general role for Rpb7 in transcription. We further show that the occupancy pattern of Rpb4, a pol II subunit that forms a subcomplex together with Rpb7, differs from those of Rpb2 and Rpb7. Rpb4 may therefore have a less general function in transcription than Rpb7. Hence, transcription by pol II is required not only for gene expression but also for repression via formation of inaccessible heterochromatin.

sted, utgiver, år, opplag, sider
Stockholm: Karolinska Institutet, 2009. s. 55
HSV kategori
Identifikatorer
urn:nbn:se:sh:diva-31550 (URN)978-91-7409-606-4 (ISBN)
Disputas
2009-12-04, Föreläsningssalen, plan 4, NOVUM, Huddinge, 10:00
Opponent
Veileder
Tilgjengelig fra: 2016-12-29 Laget: 2016-12-29 Sist oppdatert: 2016-12-29bibliografisk kontrollert

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Djupedal, IngelaBonilla, CarolinaEkwall, Karl

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