Literature DB >> 6215985

The regulation of yeast mating-type chromatin structure by SIR: an action at a distance affecting both transcription and transposition.

K A Nasmyth.   

Abstract

The two yeast mating-type alleles MATa and MAT alpha each produce two mRNAs that are transcribed in opposite and diverging directions from central promoters. Silent copies of MATa (HMRa) and MAT alpha (HML alpha) contain identical DNA sequences throughout the transcribed region, yet are not transcribed, except in sir- strains. Since SIR represses not only transcription from a silent copy but also its ability to act as a recipient in a mating-type interconversion, we have investigated whether it might act by regulating the entire chromatin structure of a silent locus. We have therefore compared the profile of DNAase I and micrococcal nuclease cleavage at HML alpha with MAT alpha and HMRa with MATa in sir- and SIR+ strains. We find that SIR is necessary for the maintenance of a different chromatin structure at HM loci from their active counterparts at MAT. One particularly striking change that SIR induces provides a simple explanation for one of its biological properties: control of directionality of switching. SIR causes the disappearance of a DNAase I-hypersensitive site at Y-Z boundary (found at MAT or HM sir-) that is coincident with a double-strand cleavage possibly created by HO in the initiation of a mating-type switch.

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Year:  1982        PMID: 6215985     DOI: 10.1016/0092-8674(82)90253-7

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  101 in total

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6.  Disruption of a silencer domain by a retrotransposon.

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Review 7.  Multifunctional DNA-binding proteins in yeast.

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8.  Trans-acting factors and properly positioned DNA elements repress mating-type genes in fission yeast.

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9.  Barrier proteins remodel and modify chromatin to restrict silenced domains.

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Journal:  Mol Cell Biol       Date:  2004-03       Impact factor: 4.272

10.  Conservative replication of double-stranded RNA in Saccharomyces cerevisiae by displacement of progeny single strands.

Authors:  R A Sclafani; W L Fangman
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