Target intelligence / Profile preview

AT-rich interaction domain-containing protein 1B (ARID1B)

Target
ARID1B
Molecular classification
Chromatin remodeling complex core subunit, SWI/SNF/BAF complex component, DNA-binding protein, Transcriptional co-regulator, Other
01

Overview

AT-rich interaction domain-containing protein 1B (ARID1B) is a DNA-binding subunit and structural core of the SWI/SNF (also called BAF) ATP-dependent chromatin remodeling complex[1][2][4][5]. This complex regulates gene expression by altering chromatin structure, enabling or restricting DNA accessibility for transcription, DNA repair, and other nuclear processes[1][2]. ARID1B is critical for normal neural development, including neural stem cell proliferation, differentiation, and neural migration[1]. Germline mutations or haploinsufficiency of ARID1B cause Coffin–Siris syndrome, a multisystem neurodevelopmental disorder characterized by intellectual disability and distinctive physical features[4][5]. ARID1B functions as a tumor suppressor, and loss of ARID1B or SWI/SNF complex integrity is implicated in various human cancers[2][5]. The protein contains an ARID DNA-binding domain and participates in switching chromatin states, often mutually exclusively with its paralog ARID1A[1][5]. No direct ARID1B-targeted therapies are currently approved, and its essential role in cell identity and proliferation means any attempted therapeutic modulation would require caution[2][5].

Other names
AT-rich interaction domain 1BAT-rich interactive domain-containing protein 1BBAF250BDAN15KIAA1235OSA2hOsa2ELD/OSA1p250R6A3-5SMARCF2BRG1-associated factor 250bBRG1-binding protein hELD/OSA1Osa homolog 2BRIGHTCSS1MRD12
02

Mechanism of action

Not applicable (no known small-molecule drugs currently target ARID1B or its immediate chromatin-remodeling function in clinical use[5])

03

Biological functions

Chromatin remodelingRegulation of gene transcriptionCell cycle controlNeural development (stem cell proliferation, neuronal differentiation, migration)Regulation of histone modificationTumor suppressionDNA repair
04

Disease associations

Cancer (frequent mutations in cancer)Neurodevelopmental disorders (Coffin–Siris syndrome)Possibly intellectual disability, autism spectrum disordersOther
05

Safety considerations

Therapeutic targeting may affect essential chromatin regulatory processes, cell differentiation, neural development, and tumor suppressionPotential risk for off-target or developmental/neurodevelopmental effects if ARID1B function is modulated
06

Biomarkers

ARID1B mutation (for Coffin–Siris syndrome diagnosis)Loss of ARID1B protein/function may serve as a biomarker in cancer genomics researchDecrease in histone acetylation (e.g., H3K9ac) as a marker in some research contexts[1]

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