Target intelligence / Profile preview

Nucleosome assembly protein 1-like 1 (NAP1L1)

Target
NAP1L1
Molecular classification
Histone chaperone, Chromatin assembly factor, Other
01

Overview

Nucleosome assembly protein 1-like 1 (NAP1L1) is a highly conserved **histone chaperone** essential for chromatin dynamics in eukaryotic cells. It mediates the nuclear import of core histones H2A-H2B, nucleosome assembly, and chromatin fluidity, thereby affecting DNA replication, repair, and global transcriptional activity[1][3]. NAP1L1 participates in both replication-coupled and replication-independent chromatin assembly and is also implicated in diverse protein interactions relevant to cell cycle, proliferation, and development. In the heart, NAP1L1 is upregulated following myocardial infarction and acts as a crucial regulator of cardiac fibrosis by promoting fibroblast proliferation and migration through stabilization of YAP1[2]. Overexpression of NAP1L1 is also noted in several cancer types and has prognostic value. No clinically approved drugs directly target NAP1L1, but its functions make it a theoretically viable target in oncology and cardiac fibrosis.

Other names
NRPhNRPNAP1NAP1LMGC8688MGC23410NAP-1-related proteinHSP22-like protein interacting protein
02

Mechanism of action

No approved drugs specifically targeting NAP1L1 are reported in the literature. NAP1L1 may indirectly modulate disease processes via histone regulation or by affecting protein ubiquitylation/proteasomal degradation pathways (e.g., Yes-associated protein 1/YAP1 in fibrosis)[2].

03

Biological functions

Chromatin assemblyHistone nuclear importDNA replicationDNA repair (nucleotide excision repair, homologous recombination)Regulation of cell proliferationNeurogenesisRegulation of transcriptionCell cycle regulationCell migration and differentiation (in cardiac fibroblasts)
04

Disease associations

Cancer (oncogene in colon cancer and lung adenocarcinoma, proliferation marker)Cardiovascular disease (cardiac fibrosis, myocardial infarction)Neurodevelopmental regulation (via neurogenesis)Infection (regulates Epstein-Barr virus reactivation)
05

Safety considerations

No drugs or inhibitors are currently in clinical use, so specific safety profiles are unknown. Targeting chromatin assembly proteins can carry theoretical risks of widespread transcriptional or proliferative effects (oncogenesis, differentiation defects)[3].
06

Biomarkers

Prognostic biomarker in colon cancer and lung adenocarcinoma (overexpression correlated with disease)

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