Activation of silent replication origins at autonomously replicating sequence elements near the HML locus in budding yeast

Citation
M. Vujcic et al., Activation of silent replication origins at autonomously replicating sequence elements near the HML locus in budding yeast, MOL CELL B, 19(9), 1999, pp. 6098-6109
Citations number
75
Categorie Soggetti
Molecular Biology & Genetics
Journal title
MOLECULAR AND CELLULAR BIOLOGY
ISSN journal
02707306 → ACNP
Volume
19
Issue
9
Year of publication
1999
Pages
6098 - 6109
Database
ISI
SICI code
0270-7306(199909)19:9<6098:AOSROA>2.0.ZU;2-3
Abstract
In the budding yeast, Saccharomyces cerevisiae, replicators can function ou tside the chromosome as autonomously replicating sequence (ARS) elements; h owever, within chromosome III, certain ARSs near the transcriptionally sile nt HML locus show no replication origin activity. Two of these ARSs compris e the transcriptional silencers E (ARS301) and I (ARS302). Another, ARS303, resides between HML and the CHA1 gene, and its function is not known. Here we further localized and characterized ARS303 and in the process discovere d a new ARS, ARS320. Both ARS303 and ARS320 are competent as chromosomal re plication origins since origin activity was seen when they were inserted at a different position in chromosome III. However, at their native locations , where the two ARSs are in a cluster with ARS302, the I silencer, no repli cation origin activity was detected regardless of yeast mating type, specia l growth conditions that induce the transcriptionally repressed CHA1 gene, trans-acting mutations that abrogate transcriptional silencing at HML (sir3 , orc5), or cis-acting mutations that delete the E and I silencers containi ng ARS elements. These results suggest that, for the HII-IL ARS cluster (AR S303, ARS320, and ARS302), inactivity of origins is independent of local tr anscriptional silencing, even though origins and silencers share key cis- a nd cans-acting components. Surprisingly, deletion of active replication ori gins located 25 kb (ORI305) and 59 kb (ORI306) away led to detection of rep lication origin function at the HML ARS cluster, as well as at ARS301, the E silencer. Thus, replication origin silencing at HML ARSs is mediated by a ctive replication origins residing at long distances from HML in the chromo some. The distal active origins are known to fire early in S phase, and we propose that their inactivation delays replication fork arrival at HML, pro viding additional time for HML ARSs to fire as origins.