Summary information and primary citation

PDB-id
8wat; SNAP-derived features in text and JSON formats; DNAproDB
Class
transcription
Method
cryo-EM (2.82 Å)
Summary
De novo transcribing complex 10 (tc10), the early elongation complex with pol ii positioned 10nt downstream of tss
Reference
Chen X, Liu W, Wang Q, Wang X, Ren Y, Qu X, Li W, Xu Y (2023): "Structural visualization of transcription initiation in action." Science, 382, eadi5120. doi: 10.1126/science.adi5120.
Abstract
Transcription initiation is a complex process, and its mechanism is incompletely understood. We determined the structures of de novo transcribing complexes TC2 to TC17 with RNA polymerase II halted on G-less promoters when nascent RNAs reach 2 to 17 nucleotides in length, respectively. Connecting these structures generated a movie and a working model. As initially synthesized RNA grows, general transcription factors (GTFs) remain bound to the promoter and the transcription bubble expands. Nucleoside triphosphate (NTP)-driven RNA-DNA translocation and template-strand accumulation in a nearly sealed channel may promote the transition from initially transcribing complexes (ITCs) (TC2 to TC9) to early elongation complexes (EECs) (TC10 to TC17). Our study shows dynamic processes of transcription initiation and reveals why ITCs require GTFs and bubble expansion for initial RNA synthesis, whereas EECs need GTF dissociation from the promoter and bubble collapse for promoter escape.

Cartoon-block schematics in six views (download the tarball)

PyMOL session file Download PDB file View in 3Dmol.js