Aug 2026· Nature Communications· Vol 17· 0 citations· 73 references
Medicine
TL;DR
This study shows that native Pol II transcription complexes are isolated directly from Drosophila melanogaster embryos by using a robust one-step affinity purification and by using cryo-EM resolve multiple functional states of the Pol II transcription complex and nucleosome.
Abstract
Structural studies of eukaryotic RNA polymerase II (Pol II) transcription often rely on in vitro assembly, which may not fully represent native conditions. To investigate Pol II transcription in metazoan cells, we developed a method to isolate native transcription complexes from Drosophila melanogaster embryos using FLAG-tag affinity purification and Micrococcal Nuclease treatment. Cryo-EM and proteomics studies revealed diverse transcription complexes and nucleosomes, including a metazoan Rpb4/Rpb7 stalk-less Pol II elongation complex and a hexameric nucleosome lacking an H2A/H2B dimer. Notably, nucleosome is found only downstream of the nucleosome elongation complex, underscoring it as a major energy barrier and a time-consuming step during Pol II progression through chromatin. Proteomics identified co-purified factors involved in transcription initiation, elongation, and RNA modification. This study provides a framework for investigations of transcription in cells, paving the way for future studies of transient and minor complexes. Here the authors show that native Pol II transcription complexes are isolated directly from D. melanogaster embryos by using a robust one-step affinity purification and by using cryo-EM resolve multiple functional states of the Pol II transcription complex and nucleosome.
Transcription occurs in the context of histone-based chromatin in eukaryotes and most archaea. The archaeal RNA polymerase and histones are ancestral to their eukaryotic counterparts, yet how RNA polymerase traverses histone-bound DNA in archaea remains poorly understood. Here, we reconstitute a nucleosome-associated t...
Gabriele Ubartaite, Daniela Tarau, A. Bula et al.· bioRxiv· 0 citations
This Review focuses on transcription by RNA polymerase II (Pol II) and discusses the integrated roles of the universal promoter scaffold factor TFIID, the transcription co-activator Mediator and the epigenetic status of the +1 nucleosome.
These findings establish ECAS as a chromatin-associated assembly that couples productive elongation with RNA processing and establishes Aqr as a highly expressed cell that profoundly impairs leukemia initiation, maintenance, and leukemia stem cell function in MLL-rearranged leukemia.
Ying Xiang, Hong-Hong Wang, Zhi-Nang Yin et al.· Molecules and Cells· 0 citations
The +1 nucleosome has emerged as a key regulator of eukaryotic transcription, but how it controls transcription initiation remains poorly understood. Here we reconstitute transcription through the +1 nucleosome using eleven purified yeast factors: RNA polymerase II (Pol II), the six general transcription factors (GTFs)...
S. Nagai, Dong-Hua Chen, Rayees U. H. Mattoo et al.· bioRxiv· 0 citations
Abstract The eukaryotic RNA polymerases (Pols) contain subunits or interact with trans-acting factors that confer robust endonuclease activity. A12.2 and C11 are subunits of Pol I and Pol III, respectively. Pol II, however, recruits transcription factor IIS (TFIIS). This evolutionary divergence of A12.2 and C11 being b...
Ryan M. Requijo, N. K. Maluf, D. Schneider et al.· Nucleic Acids Research· 0 citations
DNA replication is an exquisitely regulated process that requires tight coordination at the eukaryotic replication fork, operating within the compacted chromatin environment. Minimizing exposure of naked DNA is critical to prevent nuclease degradation and genome instability, a hallmark of cancer. Cells, therefore, requ...