Coiled-coil domain-containing 37 (FLJ40083)
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Coiled-coil domain-containing 37, also known as FLJ40083, is a protein that in humans is encoded by the CCDC37 gene (3q21.3). There is no confirmed function of CCDC37.
Gene[edit]
Locus[edit]
The human gene CCDC37 is found on chromosome 3 at the band 3q21.3.[1] It extends from base pairs 90,403,731 to 90,429,231, making the gene 25,500 base pairs long. It is located on the plus strand and contains 17 exons.[citation needed]
Homology[edit]
Paralogs[edit]
- There is only one paralog for CCDC37 found in humans, CCDC38. CCDC38 is located on chromosome 12.[2]
Orthologs[edit]
The ortholog space of CCDC37 is fairly broad including mammals, reptiles, birds, amphibians, fish, invertebrates, and fungi.[citation needed]
| Genus and species | Common name | Class | Accession | Percent identity |
|---|---|---|---|---|
| Pan troglodytes | Chimpanzee | Mammalia | XP_516716.3 | 99% |
| Otolemur crassicaudatus | Bushbaby | Mammalia | 78% | |
| Sus scrofa | Pig | Mammalia | XP_005666178.1 | 70% |
| Felis catus | Cat | Mammalia | XP_006929102.1 | 69% |
| Canis lupus | Dog | Mammalia | XP_005632343.1 | 68% |
| Mus musculus | Mouse | Mammalia | NP_776136.2 | 67% |
| Orcinus orca | Killer whale | Mammalia | XP_004285517.1 | 67% |
| Anolis carolinensis | Carolina anole | Reptilia | XP_003217822.1 | 54% |
| Python bivittatus | Burmese python | Reptilia | XP_007437868.1 | 53% |
| Chrysemys picta bellii | Painted turtle | Reptilia | XP_005288479 | 52% |
| Pseudopodoces humilis | Ground tit | Aves | XP_005522312.1 | 46% |
| Gallus gallus | Chicken | Aves | XP_425162.4 | 46% |
| Xenopus (Silurana) tropicalis | Western clawed frog | Amphibia | XP_002938271.2 | 43% |
| Astyanax mexicanus | Blind cave fish | Actinopterygii | XP_007253378.1 | 43% |
| Saccoglossus kowalevskii | Acorn worm | Enteropneusta | XP_002742365.1 | 43% |
| Ciona intestinalis | Vase tunicate | Ascidiacea | XP_002131495.1 | 43% |
| Aplysia californica | California sea slug | Gastropoda | XP_005108122.1 | 41% |
| Crassostrea gigas | Pacific oyster | Bivalvia | gbEKC37281.1 | 37% |
| Batrachochytrium dendrobatidis | Amphibian chytrid fungus | Chytridiomycetes | XP_006680088.1 | 37% |
Protein[edit]
Primary sequence[edit]
The gene encodes a protein called CCDC37. This protein in 611 amino acids in length and has a molecular weight of 71.1 kilodaltons and an isoelectric point of pI=6.7.[citation needed]
Domains[edit]
CCDC37 contains a DUF4200 region located from amino acid 151 to 269.[1] There is no known function for DUF4200. CCDC37 also contains three coiled coil domains at amino acids 164–203, 392–436, and 526–571.[3]
Post-translational modifications[edit]
The protein has several probable post-translational modifications. It contains four possible PEST sequence at amino acids 17–36, 293–304, 337–360, and 360–395.[4] It also contains a possible substrate of N-acetyltransferase A at Ser2.[5]
Signal peptides[edit]
CCDC37 has a predicted nuclear localization via Reinhard's method[6] (reliability 94.1%) using a bipartite nuclear localization signal peptide starting at amino acid 155: KRQMFLLQYALDVKRRE.[7] CCDC37 also has a few predicted nuclear export signals I232, L235, I239, and M551.[8]
Expression[edit]
CCDC37 protein is widely expressed in mus musculus but only minimally so. Most areas that express CCDC37 have an expression level of 20-40%. Expression levels in the trigeminal nerve, testis, medial olfactory epithelium, dorsal root ganglia, and trachea are the highest with almost 75% expression.[9] CCDC37 is expressed in the cerebellum, medulla, and hippocampal formation in the brain of mus musculus.[10]
Between 20 and 30 days after birth in mus musculus, CCDC37 expression increases from less than 50% to about 85%.[11]
In rattus norvegicus CCDC37 is highly expressed in oligodendrocyte progenitor cells (approximately 85%) but only narrowly expressed in oligodendrocytes themselves (~40%).[12]
Interacting proteins[edit]
Transcription factors[edit]
There are many predicted transcription factor binding sites in the CCDC37 promoter.[citation needed] Below is a table of the best possibilities, which have high confidence values, evolutionary conservation, and/or multiple possible binding sites in the promoter.
| Transcription Factor | Start | End | Strand | Sequence |
|---|---|---|---|---|
| Activator-, mediator- and TBP-dependent core promoter element for RNA polymerase II transcription from TATA-less promoters | 115 | 125 | - | ggGAGGgatcg |
| Nuclear factor 1 | 185 | 205 | + | tgctTGGCacgtggcgaataa |
| E-box binding factors | 186 | 202 | - | ttcgccaCGTGccaagc |
| E-box binding factors | 187 | 203 | + | cttggCACGtggcgaat |
| Vertebrate homologues of enhancer of split complex | 187 | 201 | - | tcgccaCGTGccaag |
| Vertebrate homologues of enhancer of split complex | 188 | 202 | + | ttggCACGtggcgaa |
| CCAAT binding factors | 203 | 217 | + | taaaCCAAtcaggat |
| E-box binding factors | 288 | 304 | + | tgggccaGGCGctgtcc |
| E-box binding factors | 352 | 368 | + | ccggcccCGCGccctcc |
| Activator-, mediator- and TBP-dependent core promoter element for RNA polymerase II transcription from TATA-less promoters | 353 | 363 | - | gcGCGGggccg |
| RNA polymerase II transcription factor II B | 358 | 364 | + | ccgCGCC |
| cAMP-responsive element binding proteins | 416 | 436 | - | tggctgTGACgccacaaaggc |
| SOX/SRY-sex/testis determining and related HMG box factors | 438 | 462 | + | cctgaAGAAtggttgccttggagac |
| X-box binding factors | 449 | 469 | - | ggtttacgtctccaAGGCaac |
| cAMP-responsive element binding proteins | 452 | 472 | - | ttgggtTTACgtctccaaggc |
| GLI-Kruppel family member GLI3 | 74 | 88 | - | atcgCCACccacact |
| "Negative" glucocoticoid response elements | 478 | 492 | - | cagctccaGGAGcag |
| Core promoter motif ten elements | 538 | 558 | - | gaccgcgAGCGcacccaccga |
| GC-Box factors SP1/GC | 564 | 580 | + | agagggGGCGcgcgggg |
| ZF5 POZ domain zinc finger | 566 | 580 | - | ccccgCGCGccccct |
| E2F-myc activator/cell cycle regulator | 566 | 582 | + | aggggGCGCgcggggtc |
Interactions[edit]
There have been three proteins found to interact by physical association with CCDC37 through a yeast two-hybrid screen: histone-lysine N-methyltransferase (SUV39H1), histone-lysine N-methyltransferase (SUV39H2), and lysine-specific histone demethylase 1A (KDM1A).[13]
Clinical significance[edit]
In a study of the genes expressed in lung squamous cell carcinomas it was found that the promoter region of CCDC37 was hyper methylated causing down regulation of the expression of CCDC37.[14] In a separate study, CCDC37 was also found in spatial and temporal regions in mice that are associated with hereditary congenital facial paresis (HCFP) gene. However through knock out experiments in mice it was found that CCDC37 was unlikely to be a causative agent for the HCFP phenotype.[15]
References[edit]
- ^ a b "CCDC37 coiled-coil domain containing 37 [Homo sapiens (human)] - Gene". Ncbi.nlm.nih.gov. Retrieved 2015-03-07.
- ^ "CCDC38 coiled-coil domain containing 38 [Homo sapiens (human)] - Gene". Ncbi.nlm.nih.gov. Retrieved 2015-03-07.
- ^ Dinkel, H. The eukaryotic linear motif resource ELM: 10 years and counting. Nucleic Acids Res. 2014 Jan;42(Database issue):D259-66.
- ^ "EMBOSS: epestfind". Emboss.bioinformatics.nl. Retrieved 2015-03-07.
- ^ Kiemer, Lars, Kyrlov Bendtsen, and Blom, Nikolai. NetAcet: Prediction of N-terminal Acetylation Sites. Bioinformatics, 2004.
- ^ A. Reinhardt and T. Hubbard, Nucleic Acids Res. 26, 2230, 1998
- ^ Dingwall C, Robbins J, Dilworth SM, Roberts B, Richardson WD (Sep 1988). "The nucleoplasmin nuclear location sequence is larger and more complex than that of SV-40 large T antigen". J. Cell Biol. 107 (3): 841–9.
- ^ Analysis and prediction of leucine-rich nuclear export signals Tanja la Cour, Lars Kiemer, Anne Mølgaard, Ramneek Gupta, Karen Skriver and Søren Brunak Protein Eng. Des. Sel., 17(6):527-36, 2004.
- ^ "4632676 - GEO Profiles - NCBI". Ncbi.nlm.nih.gov. 2014-11-12. Retrieved 2015-03-07.
- ^ Primary publication: Lein, E.S. et al. (2007) Genome-wide atlas of gene expression in the adult mouse brain, Nature 445: 168-176. doi: 10.1038/nature05453; and
- ^ "4786837 - GEO Profiles - NCBI". Ncbi.nlm.nih.gov. 2014-11-12. Retrieved 2015-03-07.
- ^ "31253706 - GEO Profiles - NCBI". Ncbi.nlm.nih.gov. 2014-11-12. Retrieved 2015-03-07.
- ^ Weimann, M. A Y2H-seq approach defines the human protein methyltransferase interactome. Nat Methods. 2013 Apr;10(4):339-42.
- ^ Kwon, Yong-Jae PhD; Lee, Seog Joo MSc et al. Genome-Wide Analysis of DNA Methylation and the Gene Expression Change in Lung Cancer Journal of Thoracic Oncology: January 2012 - Volume 7 - Issue 1 - pp 20-33.
- ^ "OMIM Entry - % 601471 - FACIAL PARESIS, HEREDITARY CONGENITAL, 1; HCFP1". Omim.org. Retrieved 2015-03-07.