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Klavs R. Hansen

Researcher at University of Copenhagen

Publications -  5
Citations -  820

Klavs R. Hansen is an academic researcher from University of Copenhagen. The author has contributed to research in topics: Schizosaccharomyces & Schizosaccharomyces pombe. The author has an hindex of 5, co-authored 5 publications receiving 762 citations. Previous affiliations of Klavs R. Hansen include Cold Spring Harbor Laboratory.

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Journal ArticleDOI

Comparative functional genomics of the fission yeasts

Nicholas Rhind, +66 more
- 20 May 2011 - 
TL;DR: Differences in gene content and regulation explain why, unlike the budding yeast of Saccharomycotina, fission yeasts cannot use ethanol as a primary carbon source and provide tools for investigation across the Schizosaccharomyces clade.
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Global Effects on Gene Expression in Fission Yeast by Silencing and RNA Interference Machineries

TL;DR: It is indicated that the RNAi and Clr proteins show only a limited functional overlap and that the ClR proteins play more global roles in gene silencing, while the wtf family of repeated sequences seems to be repressed by histone deacetylation independent of RNAi.
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The Clr7 and Clr8 Directionality Factors and the Pcu4 Cullin Mediate Heterochromatin Formation in the Fission Yeast Schizosaccharomyces pombe

TL;DR: A genetic screen for directionality mutants revealed the essential role of two previously uncharacterized factors, Clr7 and Clr8, in heterochromatin formation and suggested a role for ubiquitination at this early stage prior to the action of the Clr4 histone methyl-transferase.
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Evolutionary-conserved telomere-linked helicase genes of fission yeast are repressed by silencing factors, RNAi components and the telomere-binding protein Taz1

TL;DR: It is found that mutants lacking the histone methyltransferase Clr4, the Pcu4 cullin, Clr7 or Clr8, accumulate high levels of tlh forward and reverse transcripts, demonstrating that the tlH genes are normally repressed by heterochromatin.
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H3K9me-independent gene silencing in fission yeast heterochromatin by Clr5 and histone deacetylases.

TL;DR: It is found that Clr5 controls gene expression at multiple chromosomal locations in addition to affecting the mating-type region, and like the multi-functional Atf1 transcription factor, controls sexual differentiation and genome integrity at several levels.