Target intelligence / Profile preview

Spindle assembly abnormal protein 6 homolog (SASS6)

Target
SASS6
Molecular classification
Centriolar assembly protein, Cartwheel structural protein, Other (does not fit classic categories like receptor, enzyme, channel, transporter, etc.)
01

Overview

Spindle assembly abnormal protein 6 homolog (SASS6) is a highly conserved centriolar assembly protein that acts as the major structural component of the "cartwheel," a central scaffold required for the nine-fold symmetry of centrioles during their biogenesis. SASS6 contains a conserved N-terminal head domain, a central coiled-coil domain for dimerization, and a C-terminal region. Its assembly is essential for proper cell cycle progression and is required for centrosome function, cilia, and flagella formation. Loss or mutation of SASS6 results in abnormal centriole numbers and structure, with subsequent cell division errors, cell cycle arrest, or developmental defects such as microcephaly. High expression or aberrant function of the protein is linked to certain cancers and developmental syndromes. SASS6 does not fit into classic categories like receptor, enzyme, or transporter; it is an internal scaffold protein needed for the integrity of cell division machinery. No drugs directly target SASS6, but it remains a protein of interest for cancer and cytoskeletal research.

Other names
SASS6SAS-6SAS6HsSAS-6DKFZp761A078FLJ22097Spindle assembly defective protein 6MCPH14
02

Mechanism of action

Experimental studies suggest that inhibition or genetic knockdown leads to centriole duplication defects and cell cycle arrest.

03

Biological functions

Centriole assemblyCentriole cohesionCell cycle regulationCentrosome formationCiliary and flagellar biogenesis
04

Disease associations

Cancer (centrosome and spindle abnormalities linked to tumorigenesis)Ciliopathies (microscopic defects in centrioles impair cilia/flagellum function)Microcephaly (human MCPH14 gene variant)Other developmental defects
05

Safety considerations

Disruption leads to cell cycle arrest, cell death, and defective cell divisionTargeting may impact normal dividing cells (potential toxicity in stem cells, developing tissues, etc.)
06

Biomarkers

Overexpression or mutation status in centrosome amplification, cancer, microcephaly (experimental contexts)

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