Target intelligence / Profile preview

Establishment of sister chromatid cohesion N-acetyltransferase 1 (ESCO1)

Target
ESCO1
Molecular classification
Enzyme, Acetyltransferase, Chromatin-associated protein, Epigenetic regulator
01

Overview

Establishment of sister chromatid cohesion N-acetyltransferase 1 (ESCO1) is an enzyme that catalyzes the acetylation of the cohesin complex component SMC3, a key step in enabling the stable pairing of sister chromatids after DNA replication[1][2][3]. ESCO1 is required for maintaining sister chromatid cohesion, genome stability, and chromatin organization, particularly outside of S phase (throughout the cell cycle)[2][3][6]. It operates by modifying SMC3, supporting cohesin's role in chromosome architecture, transcriptional regulation, and DNA repair[5][6]. While its paralog ESCO2 is essential for cohesion during S phase (DNA replication), ESCO1 supports non-replicative cohesion activities and helps organize higher-order chromatin structures in cooperation with factors such as CTCF and STAG1[2][6]. Mutations or loss of ESCO1 function are implicated in developmental syndromes and may contribute to cancer[1][4][5]. **Notes/References:** - ESCO1 has no known approved drugs directly targeting it clinically[1][3]. - No established biomarkers or safety/tolerability data for ESCO1-targeted therapies have been published as of 2024[1][5].

Other names
ESCO1EFO1KIAA1911EFO1phEFO1ECO1 homolog 1ESO1 homolog 1ESO1CTF7 homolog 1Establishment factor-like protein 1Establishment of cohesion 1 homolog 1A930014I12RikCTFECO1
02

Mechanism of action

Acetylation of cohesin subunit SMC3, Regulation of cohesin-chromatin interactions, Chromatin loop organization via SMC3 and CTCF acetylation

03

Biological functions

Sister chromatid cohesionDNA replication regulationPeptidyl-lysine acetylationPost-translational protein acetylationChromatin organizationTranscriptional regulation
04

Disease associations

CancerDevelopmental disorders (e.g., Cornelia De Lange syndrome)Genome instabilityOther
05

Safety considerations

Potential for genome instability or chromosomal segregation errors if inhibited or mutatedpossible developmental defects

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