Target intelligence / Profile preview

Dynein regulatory complex subunit 7 (DRC7)

Target
DRC7
Molecular classification
Cytoskeletal protein, Axonemal protein, Structural protein, Coiled-coil protein
01

Overview

Dynein regulatory complex subunit 7 (DRC7) is a critical structural subunit of the nexin–dynein regulatory complex (N-DRC), a multi-protein assembly bridging adjacent doublet microtubules within the axoneme of motile cilia and flagella[1][3][4][6][7]. DRC7, the largest N-DRC component (~177 kDa), contains a highly conserved transglutaminase-like domain that likely interacts with glutamylated proteins in the microtubule cytoskeleton[2]. Its primary roles are maintaining the alignment and integrity of axonemal microtubule doublets, stabilizing the axonemal core, and regulating dynein-driven ciliary and flagellar movement. DRC7 is vital for proper sperm flagellum assembly, with knockout models in mice showing disorganized axonemes, immotile sperm, and infertility[1][5]. Deficiencies or mutations in DRC7 disrupt ciliary motility and structural integrity, implicating this protein in genetic forms of ciliopathies and reproductive failure, although DRC7 itself is not currently a therapeutic or diagnostic target in clinical medicine.

Other names
CCDC135CFAP50FAP50C16orf50Coiled-coil domain-containing protein 135Coiled-coil domain-containing protein lobo homolog
02

Mechanism of action

Not applicable. DRC7 is not a therapeutic drug target.

03

Biological functions

Regulation of ciliary motilityStabilization and alignment of axonemal microtubule doubletsStructural integrity and assembly of the N-DRCSperm flagellum formationSignal transduction for dynein motor activity in cilia and flagella
04

Disease associations

Male infertility (due to defective sperm motility and flagellum assembly)Ciliopathies (defects in ciliary motility, possibly primary ciliary dyskinesia and related syndromes)Other disorders of cell motility (potential pathogenic roles inferred but not yet fully characterized)

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