TY - JOUR
T1 - The comprehensive epigenome map of piRNA clusters
AU - Kawaoka, Shinpei
AU - Hara, Kahori
AU - Shoji, Keisuke
AU - Kobayashi, Maki
AU - Shimada, Toru
AU - Sugano, Sumio
AU - Tomari, Yukihide
AU - Suzuki, Yutaka
AU - Katsuma, Susumu
N1 - Funding Information:
The Program for Promotion of Basic and Applied Researches for Innovations in Bio-oriented Industry (to Su.K.); Special Coordination Funds for Promoting Science and Technology from the Ministry of Education, Culture, Sports, Science and Technology of the Japanese Government (MEXT) [22115502 to Su.K. and 17018007 to T.S., in part and the Professional Program for Agricultural Bioinformatics]; National Bio-Resource Project ‘Silkworm’ of MEXT and Grant-in-Aid for Scientific Research on Innovative Areas (Functional machinery for non-coding RNAs) (to Su.K. and Y.T.). Recipient of a fellowship from the Japan Society for the Promotion of Science (to Sh.K.). Funding for open access charge: The Program for Promotion of Basic and Applied Researches for Innovations in Bio-oriented Industry (to Su.K.).
PY - 2013/2
Y1 - 2013/2
N2 - PIWI-interacting RNA (piRNA) clusters act as antitransposon/ retrovirus centers. Integration of selfish jumping elements into piRNA clusters generates de novo piRNAs, which in turn exert trans-silencing activity against these elements in animal gonads. To date, neither genome-wide chromatin modification states of piRNA clusters nor a mode for piRNA precursor transcription have been well understood. Here, to understand the chromatin landscape of piRNA clusters and how piRNA precursors are generated, we analyzed the transcriptome, transcription start sites (TSSs) and the chromatin landscape of the BmN4 cell line, which harbors the germ-line piRNA pathway. Notably, our epigenomic map demonstrated the highly euchromatic nature of unique piRNA clusters. RNA polymerase II was enriched for TSSs that transcribe piRNA precursors. piRNA precursors possessed 50-cap structures as well as 30-poly A-tails. Collectively, we envision that the euchromatic, opened nature of unique piRNA clusters or piRNA cluster-associated TSSs allows piRNA clusters to capture new insertions efficiently.
AB - PIWI-interacting RNA (piRNA) clusters act as antitransposon/ retrovirus centers. Integration of selfish jumping elements into piRNA clusters generates de novo piRNAs, which in turn exert trans-silencing activity against these elements in animal gonads. To date, neither genome-wide chromatin modification states of piRNA clusters nor a mode for piRNA precursor transcription have been well understood. Here, to understand the chromatin landscape of piRNA clusters and how piRNA precursors are generated, we analyzed the transcriptome, transcription start sites (TSSs) and the chromatin landscape of the BmN4 cell line, which harbors the germ-line piRNA pathway. Notably, our epigenomic map demonstrated the highly euchromatic nature of unique piRNA clusters. RNA polymerase II was enriched for TSSs that transcribe piRNA precursors. piRNA precursors possessed 50-cap structures as well as 30-poly A-tails. Collectively, we envision that the euchromatic, opened nature of unique piRNA clusters or piRNA cluster-associated TSSs allows piRNA clusters to capture new insertions efficiently.
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U2 - 10.1093/nar/gks1275
DO - 10.1093/nar/gks1275
M3 - Article
C2 - 23258708
AN - SCOPUS:84873622698
SN - 0305-1048
VL - 41
SP - 1581
EP - 1590
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 3
ER -