AN IN-VITRO ASSAY FOR SACCHAROMYCES TELOMERASE REQUIRES EST1

被引:98
作者
LIN, JJ
ZAKIAN, VA
机构
[1] UNIV WASHINGTON, DEPT GENET, SEATTLE, WA 98195 USA
[2] UNIV WASHINGTON, DEPT PATHOL, SEATTLE, WA 98195 USA
关键词
D O I
10.1016/S0092-8674(05)80017-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Telomerase activity was demonstrated in cell-free extracts from S. cerevisiae through the use of a PCR-based assay. As expected, this activity was eliminated by RNase or phenol treatment of the extract and was dependent on dGTP and dTTP. Telomerase was not detected in extracts prepared from cells grown far similar to 30 or more cell divisions in the absence of the EST1 product, Est1p. TLC1 RNA, which determines the sequence of telomeric DNA in vivo, was present in normal amounts in est1 Delta cells. Moreover, TLC1 RNA specifically precipitated with epitope-tagged Est1p. These data indicate that Est1p is either a subunit of yeast telomerase or an accessory protein associated with telomerase that is essential in vitro for its activity.
引用
收藏
页码:1127 / 1135
页数:9
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