Elucidation of the mode of interaction in the UP1-telomerase RNA-telomeric DNA ternary complex which serves to recruit telomerase to telomeric DNA and to enhance the telomerase activity

We found that UP1, a proteolytic product of heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1), both enhances and represses the telomerase activity. The formation of the UP1-telomerase RNA-telomeric DNA ternary complex was revealed by a gel retardation experiment. The interactions in the ternary...

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Published inNucleic acids research Vol. 36; no. 21; pp. 6816 - 6824
Main Authors Nagata, Takashi, Takada, Yusuke, Ono, Asami, Nagata, Kayoko, Konishi, Yuki, Nukina, Takeshi, Ono, Manami, Matsugami, Akimasa, Furukawa, Ayako, Fujimoto, Natsuki, Fukuda, Hirokazu, Nakagama, Hitoshi, Katahira, Masato
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.12.2008
Oxford Publishing Limited (England)
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Summary:We found that UP1, a proteolytic product of heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1), both enhances and represses the telomerase activity. The formation of the UP1-telomerase RNA-telomeric DNA ternary complex was revealed by a gel retardation experiment. The interactions in the ternary and binary complexes were elucidated by NMR. UP1 has two nucleic acid-binding domains, BD1 and BD2. In the UP1-telomerase RNA binary complex, both BD1 and BD2 interact with telomerase RNA. Interestingly, when telomeric DNA was added to the binary complex, telomeric DNA bound to BD1 in place of telomerase RNA. Thus, BD1 basically binds to telomeric DNA, while BD2 mainly binds to telomerase RNA, which resulted in the formation of the ternary complex. Here, UP1 bridges telomerase and telomeric DNA. It is supposed that UP1/hnRNP A1 serves to recruit telomerase to telomeric DNA through the formation of the ternary complex. A model has been proposed for how hnRNP A1/UP1 contributes to enhancement of the telomerase activity through recruitment and unfolding of the quadruplex of telomeric DNA.
Bibliography:istex:256BD31AF8CDFB0B9F6C8D0F26971487B63368D4
ArticleID:gkn767
ark:/67375/HXZ-GK3HBK1L-B
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content type line 23
ISSN:0305-1048
1362-4962
DOI:10.1093/nar/gkn767