TY - JOUR
T1 - Mediator CDK subunits are platforms for interactions with various chromatin regulatory complexes
AU - Fukasawa, Rikiya
AU - Tsutsui, Taiki
AU - Hirose, Yutaka
AU - Tanaka, Aki
AU - Ohkuma, Yoshiaki
N1 - Funding Information:
This work was supported in part by Grant-in-Aid for Scientific Research (Grant # 17054022 to Y.O. and Grant # 21790066 to A.T.) and by Targeted Proteins Research Programme (to Y.O.) from the Ministry of Education, Science, and Culture of Japan, and by Grant-in-Aid for JSPS fellows (to T.T.).
PY - 2012/9
Y1 - 2012/9
N2 - The Mediator complex consists of more than 20 subunits. This is composed of four modules: head, middle, tail and CDK/Cyclin. Importantly, Mediator complex is known to play pivotal roles in transcriptional regulation, but its molecular mechanisms are still elusive. Many studies, including our own, have revealed that CDK8, a kinase subunit of the CDK/Cyclin module, is one of the key subunits involved in these roles. Additionally, we previously demonstrated that a novel CDK component, CDK19, played similar roles. It is assumed that various factors that directly affect transcriptional regulation target these two CDKs; thus, we conducted yeast two-hybrid screenings to isolate the CDK19-interacting proteins. From a screening of 40 million colonies, we obtained 287 clones that provided positive results encoded mRNAs, and it turned out that 59 clones of them encoded nuclear proteins. We checked the reading frames of the candidate clones and obtained three positive clones, all of which encoded the transcriptional cofactors, Brahma-related gene 1, B-cell CLL/lymphoma 6 and suppressor of zeste 12 homolog. Intriguingly, these three cofactors are also related to chromatin regulation. Further studies demonstrated that those could bind not only to CDK19 but also to CDK8. These results help elucidate the functional mechanism for the mutual regulations between transcription and chromatin.
AB - The Mediator complex consists of more than 20 subunits. This is composed of four modules: head, middle, tail and CDK/Cyclin. Importantly, Mediator complex is known to play pivotal roles in transcriptional regulation, but its molecular mechanisms are still elusive. Many studies, including our own, have revealed that CDK8, a kinase subunit of the CDK/Cyclin module, is one of the key subunits involved in these roles. Additionally, we previously demonstrated that a novel CDK component, CDK19, played similar roles. It is assumed that various factors that directly affect transcriptional regulation target these two CDKs; thus, we conducted yeast two-hybrid screenings to isolate the CDK19-interacting proteins. From a screening of 40 million colonies, we obtained 287 clones that provided positive results encoded mRNAs, and it turned out that 59 clones of them encoded nuclear proteins. We checked the reading frames of the candidate clones and obtained three positive clones, all of which encoded the transcriptional cofactors, Brahma-related gene 1, B-cell CLL/lymphoma 6 and suppressor of zeste 12 homolog. Intriguingly, these three cofactors are also related to chromatin regulation. Further studies demonstrated that those could bind not only to CDK19 but also to CDK8. These results help elucidate the functional mechanism for the mutual regulations between transcription and chromatin.
KW - CDK-interacting proteins
KW - Mediator
KW - chromatin regulation
KW - transcriptional cofactors
KW - transcriptional regulation
UR - http://www.scopus.com/inward/record.url?scp=84865783466&partnerID=8YFLogxK
U2 - 10.1093/jb/mvs065
DO - 10.1093/jb/mvs065
M3 - 学術論文
C2 - 22668559
AN - SCOPUS:84865783466
SN - 0021-924X
VL - 152
SP - 241
EP - 249
JO - Journal of Biochemistry
JF - Journal of Biochemistry
IS - 3
ER -