Skip NavigationSkip to Content

A DNA replication-arrest site RTS1 regulates imprinting by determining the direction of replication at mat1 in S-pombe

  1. Author:
    Dalgaard, J. Z.
    Klar, A. J. S.
  2. Author Address

    Marie Curie Res Inst, The Chart, Oxted RH8 0TL, Surrey, England. Marie Curie Res Inst, Oxted RH8 0TL, Surrey, England. NCI, Frederick Canc Res & Dev Ctr, Dept Hlth & Human Serv, Div Basic Sci, Gene Regulat & Chromosome Biol Lab, Frederick, MD 21701 USA. Dalgaard JZ Marie Curie Res Inst, The Chart, Oxted RH8 0TL, Surrey, England.
    1. Year: 2001
  1. Journal: Genes & Development
    1. 15
    2. 16
    3. Pages: 2060-2068
  2. Type of Article: Article
  1. Abstract:

    Mating-type switching in Schizosaccharomyces pombe involves a strand-specific, alkali-labile imprint at the mat1 (mating- type) locus. The imprint is synthesized during replication in a swi1, swi3, and polyinerase alpha (swi7) dependent manner and is dependent on mat1 being replicated in a specific direction. Here we show that the direction of replication at mat1 is controlled by a cis-acting polar terminator of replication (RTS1). Two-dimensional gel analysis of replication intermediates reveals that RTS1 only terminates replication forks moving in the centromere-distal direction. A genetic analysis shows that RTS1 optimizes the imprinting process. Transposing the RTS1 element to the distal side of mat1 abolishes imprinting of the native mat1 allele but restores imprinting of an otherwise unimprinted inverted mat1 allele. These data provide conclusive evidence for the "direction of replication model" that explains the asymmetrical switching pattern of S. pombe, and identify a DNA replication-arrest element implicated in a developmental process. Such elements could play a more general role during development and differentiation in higher eukaryotes by regulating the direction of DNA replication at key loci.

    See More

External Sources

  1. DOI: 10.1101/gad.200801
  2. PMID: 11511538
  3. PMCID: PMC312760

Library Notes

  1. No notes added.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel