Target intelligence / Profile preview

Leucine zipper protein 1 (LUZP1)

Target
LUZP1
Molecular classification
Actin cross-linking protein, Centrosomal protein, Cytoskeletal regulatory protein, Other (not a classical receptor, ion channel, enzyme, or transcription factor)
01

Overview

Leucine zipper protein 1 (LUZP1) is a cytoskeletal regulatory protein containing leucine zipper motifs and cross-linking domains that stabilize filamentous actin (F-actin) and regulate actin filament dynamics[4][3][2]. It localizes to the centrosome, actin cytoskeleton, and midbody, acting as a negative regulator of ciliogenesis and playing key roles in cell migration, division, and embryonic development[4][2][5][6]. Deletion or mutation of LUZP1 leads to cytoskeletal and ciliary abnormalities, with implications for congenital diseases (e.g., chromosome 1p36 deletion syndrome, Townes-Brocks syndrome) and potential contributions to cancer mechanisms by affecting cell invasion and migration[4][3][2]. LUZP1 interacts with other cytoskeletal proteins such as filamin A, ARP2, and ARP3, and contributes to the stabilization of chromatin remodeling complexes, but is not a validated target for pharmacological intervention[4][6][5].

Other names
LUZP1LUZPFimbacinFilamin mechanobinding actin cross-linking proteinfimbacin
02

Biological functions

Regulation of actin cytoskeleton stability and F-actin bundlingNegative regulation of primary cilia formation (ciliogenesis)Regulation of cell migration and invasionRegulation of cell division and nuclear sizeEmbryonic brain and cardiovascular development
03

Disease associations

Chromosome 1p36 deletion syndrome (complete deletion can contribute to phenotype)Townes-Brocks syndrome (in context of ciliopathy and cytoskeletal dysfunction)Cancer (frequent gene deletions; possible association with tumor invasion and migration)Developmental defects (neural tube closure, heart defects)

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