Rfc5p regulates alternate RFC complex functions in sister chromatid pairing reactions in budding yeast.
Rfc5p regulates alternate RFC complex functions in sister chromatid pairing reactions in budding yeast.
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DOI:
10.4161/cc.9.21.13634
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发表时间:
2010-11-01
期刊:
影响因子:
--
通讯作者:
Skibbens RV
中科院分区:
文献类型:
--
作者:
Maradeo ME;Garg A;Skibbens RV
Sister chromatid pairing reactions, termed cohesion establishment, occur during S-phase and appear to be regulated by Replication Factor C (RFC) complexes. For instance, RFCs that contain Ctf18p exhibit pro-establishment activities while those that contain Elg1p exhibit anti-establishment activities. It remains unknown whether Ctf18p-RFC and Elg1p-RFC functions are simply opposing or instead reveal complicated and non-parallel regulatory mechanisms. To better understand the nature of these novel pathways, we analyzed the small RFC subunit Rfc5p that is common to both Ctf18p-RFC and Elg1p-RFC. Despite this commonality, the data show that diminished Rfc5p function rescues ctf7/eco1 mutant cell phenotypes, revealing that Rfc5p promotes anti-establishment activities. This rescue is specific to establishment pathways in that rfc5-1 greatly accentuates growth defects when expressed in scc2 (deposition), mcd1/scc1 or smc3 (cohesion maintenance) mutated cells. Our results reveal for the first time a role for small RFC subunits in directing RFC complex functions – in this case towards anti-establishment pathways. We further report that Pds5p exhibits both establishment and anti-establishment functions in cohesion. This duality suggests that categorizations of establishment and anti-establishment activities require further examination.
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DOI:
10.1073/pnas.1434308100
发表时间:
2003-09-02
影响因子:
11.1
作者:
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通讯作者:
Hurwitz, J
影响因子:
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作者:
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DOI:
10.1083/jcb.151.3.613
发表时间:
2000-10-30
期刊:
The Journal of cell biology
影响因子:
--
作者:
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通讯作者:
Guacci V
影响因子:
16
作者:
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通讯作者:
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