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. 1991 Nov 25;19(22):6255-62.
doi: 10.1093/nar/19.22.6255.

Analysis of the interactions of functional domains of a nuclear origin of replication from Saccharomyces cerevisiae

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Free PMC article

Analysis of the interactions of functional domains of a nuclear origin of replication from Saccharomyces cerevisiae

S S Walker et al. Nucleic Acids Res. .
Free PMC article

Abstract

We have determined that ARS121 is an efficient origin of replication on chromosome X of Saccharomyces cerevisiae. This origin is comprised of at least three distinct functional domains. One of these domains is the ARS121 core sequence (approximately 35 bp-long), which is essential for origin activity. This essential core contains an 11 bp sequence resembling (2 bp mismatch) the ARS consensus. Another important domain is an enhancer of DNA replication, which binds the OBF1 protein. The third domain, ATR (A/T-rich, approximately 72 bp), is auxiliary and works in either orientation, but only when located 3' to the essential core. When fused to the ARS121 core both the enhancer and the ATR domain act synergistically to enhance the activity of the origin. Furthermore, when fused to the essential core sequences of heterologous ARSs, ARS1 and ARS307, the auxiliary domains also appeared to stimulate synergistically origin function. These results suggest that (i) in order to elicit maximal origin activity all three domains have to interact and (ii) activation of the essential core sequences at different origins of replication may share a common mechanism.

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References

    1. Cell. 1984 May;37(1):299-307 - PubMed
    1. Genetics. 1984 Mar;106(3):365-85 - PubMed
    1. Nucleic Acids Res. 1986 Aug 11;14(15):6247-64 - PubMed
    1. Mol Cell Biol. 1986 Apr;6(4):1148-57 - PubMed
    1. Mol Cell Biol. 1986 Jul;6(7):2354-63 - PubMed

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