The conserved AAUAAA hexamer of the poly (A) signal can act alone to trigger a stable decrease in RNA polymerase II transcription velocity

A Nag, K Narsinh, A Kazerouninia, HG Martinson - RNA, 2006 - rnajournal.cshlp.org
In vivo the poly (A) signal not only directs 3′-end processing but also controls the rate and
extent of transcription. Thus, upon crossing the poly (A) signal RNA polymerase II first …

Splicing-and cleavage-independent requirement of RNA polymerase II CTD for mRNA release from the transcription site

N Custódio, M Vivo, M Antoniou… - The Journal of cell …, 2007 - rupress.org
Eukaryotic cells have a surveillance mechanism that identifies aberrantly processed pre-
mRNAs and prevents their flow to the cytoplasm by tethering them near the site of …

Transcription and splicing: when the twain meet

Y Brody, Y Shav-Tal - Transcription, 2011 - Taylor & Francis
Splicing can occur co-transcriptionally. What happens when the splicing reaction lags after
the completed transcriptional process? We found that elongation rates are independent of …

Hexameric architecture of CstF supported by CstF-50 homodimerization domain structure

M Moreno-Morcillo, L Minvielle-Sébastia, C Mackereth… - RNA, 2011 - rnajournal.cshlp.org
The Cleavage stimulation Factor (CstF) complex is composed of three subunits and is
essential for pre-mRNA 3′-end processing. CstF recognizes U and G/U-rich cis-acting RNA …

Structural basis to stabilize the domain motion of BARD1-ARD BRCT by CstF50

RK Choudhary, MQ Siddiqui, PS Thapa, N Gadewal… - Scientific Reports, 2017 - nature.com
BRCA1 associated ring domain protein 1 (BARD1) is a tumor suppressor protein having a
wide role in cellular processes like cell-cycle checkpoint, DNA damage repair and …

Targeting tat inhibitors in the assembly of human immunodeficiency virus type 1 transcription complexes

I D'Orso, JR Grunwell, RL Nakamura, C Das… - Journal of …, 2008 - Am Soc Microbiol
Human immunodeficiency virus type 1 (HIV-1) transcription is regulated by the viral Tat
protein, which relieves a block to elongation by recruiting an elongation factor, P-TEFb, to …

Localization of RNAPII and 3′ end formation factor CstF subunits on C. elegans genes and operons

A Garrido-Lecca, T Saldi, T Blumenthal - Transcription, 2016 - Taylor & Francis
Transcription termination is mechanistically coupled to pre-mRNA 3′ end formation to
prevent transcription much beyond the gene 3′ end. C. elegans, however, engages in …

Prolonged α-amanitin treatment of cells for studying mutated polymerases causes degradation of DSIF160 and other proteins

DC Tsao, NJ Park, A Nag, HG Martinson - Rna, 2012 - rnajournal.cshlp.org
A useful method for studying the function of the mammalian RNA polymerase II takes
advantage of the extreme sensitivity of its largest subunit, Rpb1, to α-amanitin. Mutations of …

RNA polymerase II phosphorylation and gene expression regulation

O Calvo, A García - Protein Phosphorylation in Human Health, 2012 - books.google.com
RNA polymerases (RNAPs) are among the most important cellular enzymes. They are
present in all living organisms from Bacteria and Archaea to Eukarya and are responsible for …

[PDF][PDF] A Potential Effect of Cordycepin on the Feedback between Polyadenylation and PI3K/Akt/mTOR Signalling

S Lawrence - 2023 - core.ac.uk
Polyadenylation is a key step in mRNA maturation and leads to the sequential addition of
adenosines forming a poly (A) tail, which is important in mRNA stability, nuclear export …