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Involvement of Telomerase Reverse Transcriptase in Heterochromatin Maintenance
Author(s) -
Yoshiko Maida,
Mami Yasukawa,
Naoko Okamoto,
Seii Ohka,
Keita Kinoshita,
Yasushi Totoki,
Takashi Ito,
Tohru Minamino,
Hiromi Nakamura,
Satoko Yamaguchi,
Tatsuhiro Shibata,
Kenkichi Masutomi
Publication year - 2014
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.00093-14
Subject(s) - heterochromatin , biology , rna induced transcriptional silencing , heterochromatin protein 1 , schizosaccharomyces , telomerase , telomerase reverse transcriptase , telomerase rna component , rna , telomere , rna interference , genetics , microbiology and biotechnology , schizosaccharomyces pombe , dna , chromatin , gene , saccharomyces cerevisiae
In the fission yeastSchizosaccharomyces pombe , centromeric heterochromatin is maintained by an RNA-directed RNA polymerase complex (RDRC) and the RNA-induced transcriptional silencing (RITS) complex in a manner that depends on the generation of short interfering RNA. In association with the telomerase RNA component (TERC), the telomerase reverse transcriptase (TERT) forms telomerase and counteracts telomere attrition, and without TERC, TERT has been implicated in the regulation of heterochromatin at locations distinct from telomeres. Here, we describe a complex composed of human TERT (hTERT), Brahma-related gene 1 (BRG1), and nucleostemin (NS) that contributes to heterochromatin maintenance at centromeres and transposons. This complex produced double-stranded RNAs homologous to centromeric alpha-satellite (alphoid ) repeat elements and transposons that were processed into small interfering RNAs targeted to these heterochromatic regions. These small interfering RNAs promoted heterochromatin assembly and mitotic progression in a manner dependent on the RNA interference machinery. These observations implicate the hTERT/BRG1/NS (TBN) complex in heterochromatin assembly at particular sites in the mammalian genome.

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