NUBP2
NUBP iron-sulfur cluster assembly factor 2, cytosolic
- Ensembl:
- ENSG00000095906
- UniProt:
- Q9Y5Y2
- OMIM:
- 610779
- Synonyms:
- CFD1, CIAO6
Cilia effects upon perturbation of NUBP2
- Cilia number / % ciliated:
- Incrased cilia number
Ciliogenesis screen results (3 screens)
- Wheway et al. 2015 (siRNA) [siRNA]: Ciliogenesis Defect (z=-5.94) PMID:26167766
- Breslow et al. 2018 (CRISPR) [CRISPR]: Increased Signaling (Negative Regulator) PMID:29459680
- Roosing et al. 2015 (siRNA) [siRNA]: No effect PMID:26595381
Phenotypes
- Mouse phenotype:
- increased circulating fructosamine level, preweaning lethality, complete penetrance, decreased total reti thickness
- Mouse ciliopathy phenotype:
- short tibia
Subcellular localization
basal body, centrosome, nucleus
Functional category
- Ciliary assembly/disassembly
- T cell biology
Function
Nubp1 and Nubp2 interact with each other, but their individual knockdown, however, has differential effects on centrosome and spindle formation: while Nubp1 silencing qualitatively phenocopies KIFC5A silencing, also resulting in significant centrosome amplification throughout the cell cycle and the formation of multipolar spindles, Nubp2 appears to have a modulatory/accessory role for centriole arithmetics, in concert with KIFC5A and Nubp1 [16638812]. Nubp1 and Nubp2 localize on interphase centrioles in cycling cells and basal bodies in quiescent cells(23807208).
Model organism evidence
Premature differentiation of neurons is associated with defects in the centrosome and/or primary cilia.
NUBP2 is implicated in both the cytosolic iron/sulfur cluster assembly pathway and negative regulation of ciliogenesis.
The nucleotide-binding proteins Nubp1 and Nubp2 are negative regulators of ciliogenesis.
PMIDs: 23807208