Capicua transcriptional repressor is a
protein that in humans is encoded by the CICgene.[5][6][7] Capicua functions as a
transcriptional repressor in a way that ensures its impact on the progression of cancer, and plays a significant role in the operation of the central nervous system through its interaction with
ataxin 1. The name of the protein derives from the
Catalan expression cap-i-cua which literally translates to "head-and-tail".[8]
Structure
Capicua is a
highly conserved protein, with a lot of similarity between human and Drosophila melanogaster homologs.[9] In the human body, capicua exists in two isoforms, the short (CIC-S) and the long (CIC-L) one, which differ in their
N-terminal section. The two evolutionarily conserved
domains of the protein are HMG-box (high-mobility group box) and the
C1 domain: they work together to recognize specific octameric
DNA sequences.[9] Capicua also contains a
nuclear localisation sequence that allows it to enter the
nucleus of the cell.
Capicua forms a complex with
ataxin 1 (CIC-ATXN1 complex) and owing to this interaction it plays a crucial role in the development of
spinocerebellar ataxia type 1. While in a healthy organism this complex serves to ensure correct cellular function, in patients with ATXN1 mutations a modified complex has a toxic effect on cerebellar cells, resulting in the motor symptoms typical for this disorder.[9] Blocking the formation of the complex in a murine model of ataxia reduces the symptoms.
Tumors
CIC has been shown to act as a
tumor suppressor in numerous types of cancer,[9] and, vice versa, mutations of CIC have been found in some types of tumors. According to a review published in 2020, CIC mutations were most often discovered in oligodendroglioma.[9] A genomic
translocation resulting in the formation of a hybrid CIC-
DUX4 gene may cause an aggressive
Ewing-like
sarcoma.[11] Instead of acting as a suppressor, a hybrid protein produced by fusion of CIC and DUX4 has been shown to act as an activator of genes.[12]
According to a review published in 2017, the CIC gene is deleted in 46-53% of analyzed
oligodendroglioma tumors as part of the
1p/19q codeletion, a mutation that may also affect the
FUBP1 gene.[13]
The CIC gene was first identified in Drosophila in 2000.[9] It was shown to encode a
transcriptional repressor participating in the regulation of
embryogenesis. In a mutated fly which at the embryonic stage had only the first and the last segments present, with the intermediate segments missing, scientists discovered a mutation of the CIC gene, and this prompted them to call the protein capicua ("head-and-tail" in Catalan).
Interactions
FOLR1 — capicua has been shown to affect the expression of folate receptor alpha, and CIC mutations might result in cerebral folate deficiency.[15]
ATXN1 — capicua and ataxin 1 form a complex (ATXN1-CIC) which is crucial for proper brain development.[10]
DUX4 – chimeric CIC-DUX4 proteins are found in tumors.[10]
FOXO4 – chimeric CIC-FOXO4 proteins are found in tumors.[12]
NUTM1 – chimeric CIC-NUTM1 proteins are found in tumors.[12]
LEUTX – chimeric CIC-LEUTX proteins are found in tumors.[12]
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Lee CJ, Chan WI, Cheung M, Cheng YC, Appleby VJ, Orme AT, Scotting PJ (Oct 2002). "CIC, a member of a novel subfamily of the HMG-box superfamily, is transiently expressed in developing granule neurons". Brain Res Mol Brain Res. 106 (1–2): 151–6.
doi:
10.1016/S0169-328X(02)00439-4.
PMID12393275.
^Lee CJ, Chan WI, Scotting PJ (Jun 2005). "CIC, a gene involved in cerebellar development and ErbB signaling, is significantly expressed in medulloblastomas". J Neurooncol. 73 (2): 101–8.
doi:
10.1007/s11060-004-4598-2.
PMID15981098.
S2CID24938086.
^
abcLu HC, Tan Q, Rousseaux MW, Wang W, Kim JY, Richman R, Wan YW, Yeh SY, Patel JM, Liu X, Lin T, Lee Y, Fryer JD, Han J, Chahrour M, Finnell RH, Lei Y, Zurita-Jimenez ME, Ahimaz P, Anyane-Yeboa K, Van Maldergem L, Lehalle D, Jean-Marcais N, Mosca-Boidron AL, Thevenon J, Cousin MA, Bro DE, Lanpher BC, Klee EW, Alexander N, Bainbridge MN, Orr HT, Sillitoe RV, Ljungberg MC, Liu Z, Schaaf CP, Zoghbi HY (April 2017).
"Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans". Nature Genetics. 49 (4): 527–536.
doi:
10.1038/ng.3808.
PMC5374026.
PMID28288114.