Target intelligence / Profile preview

Bromodomain-containing protein 1 (BRD1)

Target
BRD1
Molecular classification
Epigenetic reader, Transcription coactivator, Chromatin remodeling factor, BET (Bromodomain and Extra-Terminal motif) family, Histone modification–associated protein
01

Overview

Bromodomain-containing protein 1 (BRD1) is a member of the bromodomain protein family, characterized by the presence of a bromodomain that specifically recognizes acetylated lysine residues on histone tails, enabling the regulation of gene transcription through chromatin remodeling. BRD1 acts as a scaffold in the assembly of multi-protein chromatin complexes and exerts broad influence over epigenetic and transcriptional regulation. Dysfunction or altered expression of BRD1 is implicated in the pathogenesis of cancer, neurodevelopmental, and psychiatric disorders. As a member of the wider bromodomain protein class, BRD1 is considered a candidate therapeutic target, particularly as the role of epigenetic readers in disease becomes increasingly understood. Several small molecule inhibitors targeting the bromodomain family are under active investigation, particularly for oncology and inflammatory indications, though none specifically selective for BRD1 have reached clinical approval[1][3][5][6][7].

Other names
BRD1BROMO DOMAIN CONTAINING 1KIAA0368BRD1A
02

Mechanism of action

Inhibitors block the interaction between bromodomain and acetylated lysine residues, leading to altered transcriptional programs, especially silencing genes involved in proliferation and inflammation

03

Biological functions

Recognition of acetylated lysine on histone tailsRegulation of gene transcriptionScaffold for multi-protein chromatin complexesChromatin remodelingTranscriptional activation and mediationCell cycle controlMay be contextually involved in DNA damage response or replication
04

Disease associations

CancerNeurodevelopmental disordersPsychiatric disordersInflammationSome evidence for involvement in obesity and multiple sclerosis
05

Safety considerations

On-target effects on global transcriptional regulation can result in hematologic and gastrointestinal toxicities (drawn from BET inhibitor class effects)Potential neurocognitive or psychiatric effects due to roles in neural development
06

Interacting drugs

Selective inhibitors for bromodomain proteins (under development)

4 more in the full profile.

07

Biomarkers

BRD1 expression levelHistone acetylation patterns (indirectly)MYC expression (for BET inhibitors)Select fusion proteins (e.g., in NUT midline carcinoma, for BET inhibitors)No robust BRD1-selective biomarker established

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