Target intelligence / Profile preview

Akirin-1 (AKIRIN1)

Target
AKIRIN1
Molecular classification
Transcription cofactor / adapter protein, Nuclear protein
01

Overview

Akirin-1 is a small (~22 kDa), highly conserved nuclear protein that acts as a transcriptional cofactor or molecular adapter, primarily facilitating communication between signaling pathways, chromatin remodelers, and transcription factors involved in gene regulation[1][2][3]. It is particularly important in skeletal muscle development and regeneration, where it mediates pathways controlling myoblast differentiation and migration, responding to signals such as myostatin (MSTN). Although Akirin-1 does not contain recognizable DNA-binding or catalytic domains, it orchestrates protein-protein interactions central to gene expression regulation. Unlike its paralog Akirin-2, Akirin-1 is non-essential for embryonic survival in mice, but its deficiency influences muscle fiber phenotype and regeneration efficiency. Disease associations include rare congenital myopathies. There is no evidence that Akirin-1 is currently targeted directly by any drugs or used as a clinical biomarker[1][2][3].

Other names
C1orf108FLJ12666STRF2Mighty (in earlier literature)Akirin-1AKIRIN1
02

Mechanism of action

Not applicable: No drugs target Akirin-1

03

Biological functions

Regulation of gene expression (acts as a transcriptional cofactor via protein-protein interactions, not by direct DNA binding)Skeletal muscle development and myogenesis regulation (involved in myoblast differentiation and migration, modulates satellite cell function)Regulator of actin cytoskeleton reorganization, impacting lamellipodium formation and cell migrationSignal transduction in response to myostatin (MSTN) during muscle regeneration
04

Disease associations

Myopathy, centronuclear, 1Nemaline myopathy 10Implicated in muscle development disorders and possibly tumorigenesis (though more evidence for the latter pertains to AKIRIN2)No direct evidence for roles in cancer, inflammation, neurodegeneration, cardiovascular disease, or infection for AKIRIN1 in human therapeutics, though general involvement in cell survival and muscle function is reported

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