TY - JOUR
T1 - A noncoding RNA containing a SINE-B1 motif associates with meiotic metaphase chromatin and has an indispensable function during spermatogenesis
AU - Nakajima, Ryusuke
AU - Sato, Takuya
AU - Ogawa, Takehiko
AU - Okano, Hideyuki
AU - Noce, Toshiaki
N1 - Funding Information:
We thank Drs. Sawako Ina and Naoki Tsunekawa, and Ms. Aya Nakamura and Ako Tokumasu (former Mitsubishi-Kagaku Institute of Life Science) for their technical help. This study was supported by Grant-in-Aids from the Japan Society for the Challenging Research Exploratory (to T.N.) and the Promotion of Science Research Fellowship Program (to R.N.).
Publisher Copyright:
© 2017 Nakajima et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2017/6
Y1 - 2017/6
N2 - A search for early response genes that are activated following germ cell induction from mouse embryonic stem cells in vitro led us to the isolation of a long noncoding RNA that contains a SINE (short interspersed element)-B1F motif that was named R53. In situ hybridization and northern blot analyses revealed that the R53 subfragment RNA bears a B1F motif, is processed from the primary transcript, is expressed in adult testis and is predominantly localized in meiotic metaphase chromatin during spermatogenesis. Recent studies of chromosome- associated RNAs have explored novel functions of noncoding RNAs. Specifically, chromosome-bound noncoding RNAs function not only as structural components of chromosome but also as scaffolds that recruit epigenetic modulators for transcriptional regulation, and they are dynamically rearranged during the cell cycle. However, few studies have explored meiotic chromatin; thus, R53 RNA appears to be the first long noncoding RNA to be tightly associated with the metaphase chromatin during spermatogenesis. Furthermore, R53 knockdown using a lentivirus-mediated RNAi injected into mouse testis and organ culture of the fragments revealed a remarkable reduction in postmeiotic cells and irregular upregulation of several postmeiotic genes, which suggests the possibility that the SINE-B1- derived noncoding RNA R53 plays an indispensable role in the transcriptional regulation of key spermatogenesis genes.
AB - A search for early response genes that are activated following germ cell induction from mouse embryonic stem cells in vitro led us to the isolation of a long noncoding RNA that contains a SINE (short interspersed element)-B1F motif that was named R53. In situ hybridization and northern blot analyses revealed that the R53 subfragment RNA bears a B1F motif, is processed from the primary transcript, is expressed in adult testis and is predominantly localized in meiotic metaphase chromatin during spermatogenesis. Recent studies of chromosome- associated RNAs have explored novel functions of noncoding RNAs. Specifically, chromosome-bound noncoding RNAs function not only as structural components of chromosome but also as scaffolds that recruit epigenetic modulators for transcriptional regulation, and they are dynamically rearranged during the cell cycle. However, few studies have explored meiotic chromatin; thus, R53 RNA appears to be the first long noncoding RNA to be tightly associated with the metaphase chromatin during spermatogenesis. Furthermore, R53 knockdown using a lentivirus-mediated RNAi injected into mouse testis and organ culture of the fragments revealed a remarkable reduction in postmeiotic cells and irregular upregulation of several postmeiotic genes, which suggests the possibility that the SINE-B1- derived noncoding RNA R53 plays an indispensable role in the transcriptional regulation of key spermatogenesis genes.
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U2 - 10.1371/journal.pone.0179585
DO - 10.1371/journal.pone.0179585
M3 - Article
C2 - 28658256
AN - SCOPUS:85021623450
SN - 1932-6203
VL - 12
JO - PloS one
JF - PloS one
IS - 6
M1 - e0179585
ER -