Evidence map›Paper›PMID 40463266›Full record

ArticlebioRxiv : the preprint server for biology2025

The extra-terminal domain drives the role of BET proteins in transcription.

Iwona Pasionek, Agnieszka Machowska, John B Ridenour, Magdalena Donczew, Rafal Donczew

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Iwona PasionekCell Cycle and Cancer Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, 73104, OK, USA.
Agnieszka MachowskaCell Cycle and Cancer Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, 73104, OK, USA.
John B RidenourCell Cycle and Cancer Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, 73104, OK, USA.
Magdalena DonczewCell Cycle and Cancer Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, 73104, OK, USA.
Rafal DonczewCell Cycle and Cancer Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, 73104, OK, USA.

Funding

Understanding connective tissue development and disease with PDGFR-driven..... P20GM103636 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI THOMPSON, LINDA F · 2013 to 2023
$26.9M
NIGMS NIH HHS P20 GM103636
6 · The paper itself

Abstract

BET proteins facilitate transcription of most eukaryotic genes but the specific mechanisms by which BET proteins perform their functions remain poorly understood. As chromatin readers, BET proteins use their tandem bromodomains to interact with acetylated lysine residues on histones and other protein partners. However, recent findings illustrate that bromodomain activity does not fully explain BET protein roles in transcription, highlighting the significance of other BET protein domains. We evaluated the importance of all conserved domains of BET proteins and determined that the extra-terminal (ET) domain is essential for cell viability, genome-wide transcription and BET protein chromatin occupancy. Furthermore, we provide evidence that the ET domain performs these functions serving as a hub for interactions with other factors involved in transcription regulation. Our findings expand current understanding of the complex biology of BET proteins and suggest the mechanisms by which cells can bypass bromodomain inhibition in pathologic states.

Identifiers

PMID40463266
PMCPMC12132590

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.