TY - JOUR
T1 - The Nuclear Pore-Associated TREX-2 Complex Employs Mediator to Regulate Gene Expression
AU - Schneider, Maren
AU - Hellerschmied, Doris
AU - Schubert, Tobias
AU - Amlacher, Stefan
AU - Vinayachandran, Vinesh
AU - Reja, Rohit
AU - Pugh, B. Franklin
AU - Clausen, Tim
AU - Köhler, Alwin
N1 - Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2015/8/27
Y1 - 2015/8/27
N2 - Summary Nuclear pore complexes (NPCs) influence gene expression besides their established function in nuclear transport. The TREX-2 complex localizes to the NPC basket and affects gene-NPC interactions, transcription, and mRNA export. How TREX-2 regulates the gene expression machinery is unknown. Here, we show that TREX-2 interacts with the Mediator complex, an essential regulator of RNA Polymerase (Pol) II. Structural and biochemical studies identify a conserved region on TREX-2, which directly binds the Mediator Med31/Med7N submodule. TREX-2 regulates assembly of Mediator with the Cdk8 kinase and is required for recruitment and site-specific phosphorylation of Pol II. Transcriptome and phenotypic profiling confirm that TREX-2 and Med31 are functionally interdependent at specific genes. TREX-2 additionally uses its Mediator-interacting surface to regulate mRNA export suggesting a mechanism for coupling transcription initiation and early steps of mRNA processing. Our data provide mechanistic insight into how an NPC-associated adaptor complex accesses the core transcription machinery.
AB - Summary Nuclear pore complexes (NPCs) influence gene expression besides their established function in nuclear transport. The TREX-2 complex localizes to the NPC basket and affects gene-NPC interactions, transcription, and mRNA export. How TREX-2 regulates the gene expression machinery is unknown. Here, we show that TREX-2 interacts with the Mediator complex, an essential regulator of RNA Polymerase (Pol) II. Structural and biochemical studies identify a conserved region on TREX-2, which directly binds the Mediator Med31/Med7N submodule. TREX-2 regulates assembly of Mediator with the Cdk8 kinase and is required for recruitment and site-specific phosphorylation of Pol II. Transcriptome and phenotypic profiling confirm that TREX-2 and Med31 are functionally interdependent at specific genes. TREX-2 additionally uses its Mediator-interacting surface to regulate mRNA export suggesting a mechanism for coupling transcription initiation and early steps of mRNA processing. Our data provide mechanistic insight into how an NPC-associated adaptor complex accesses the core transcription machinery.
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U2 - 10.1016/j.cell.2015.07.059
DO - 10.1016/j.cell.2015.07.059
M3 - Article
C2 - 26317468
AN - SCOPUS:84940504501
SN - 0092-8674
VL - 162
SP - 1016
EP - 1028
JO - Cell
JF - Cell
IS - 5
ER -