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Ccdc60

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Ccdc60
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Coiled-coil domain containing 60 is a protein that in humans is encoded by the CCDC60 gene that is most highly expressed in the trachea, salivary glands, bladder, cervix, and epididymis.[5]

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Gene

The gene that encodes CCDC60 is located on the plus strand of chromosome 12 (12q24.23) and contains 14 exons.[6] The gene spans positions 119334712-119541047.[7] The first record of the gene that encodes CCDC60 in the NCBI nucleotide database originated from a data set containing 15,000 human and mouse full-length cDNA sequences.[6]

Protein

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Predicted structure of CCDC60.[8]

CCDC60 is made up of 550 amino acids.[9] The computational isoelectric point of CCDC60 is 9.17 and the computational molecular weight is approximately 63kDa.[10] Western blots of RT-4 and U-251 cell lines support the predicted molecular weight.[11] The predicted subcellular location of CCDC60 is the mitochondria.[12] The secondary structure of CCDC60 contains a namesake coiled-coil domain in addition to predicted alpha helices and coils.[13]

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Regulation

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Gene expression

The expression of CCDC60 is tissue-specific. CCDC60 is most highly expressed in the trachea, salivary glands, bladder, cervix, and epididymis.[5] CCDC60 is also expressed in epithelial cells of the upper respiratory system.[14] RNA seq data shows relatively high levels of expression in the prostate, moderate expression in the lungs and ovaries, and low expression in the colon, adrenal gland, and brain.[15]

Transcription factors

There are many candidate transcription factors that bind to the promoter region of the gene that encodes CCDC60.[16]

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Post-translational modification

CCDC60 is a candidate for phosphorylation by Protein kinase C.[17] The initial methionine residue is predicted to be cleaved from the polypeptide after translation.[18]

Evolutionary history

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Orthologs

The most distantly related organism in which a likely ortholog to Human CCDC60 can be found in is Amphimedon queenslandica, a sea sponge. Orthologs to Human CCDC60 are not found in any prokaryotes. Interestingly, there are no known orthologs in arthropods, although there are many other invertebrates that possess likely orthologs.

CCDC60 Orthologs
Organism Taxonomic Group Divergence (MYA)[19] Accession Number Sequence Length Shared Sequence Identity[20]
Human Hominidae 0 NP_848594.2 550 100%
Philippine tarsier Tarsiidae 67 XP_008067500.1 559 77.29%
Gray mouse lemur Lemuriformes 73 XP_012612137.1 548 77.60%
Yellow-bellied marmot Rodentia 90 XP_027779037.1 559 76.32%
Sea otter Carnivora 96 XP_022373045.1 548 84.90%
Florida Manatee Placentalia 105 XP_004379174.1 551 83.64%
Common wombat Marsupialia 159 XP_027721296.1 564 62.86%
Southern Ostrich Aves 312 XP_009685824.1 489 37.03%
Bald eagle Aves 320 XP_010573943.1 661 32.02%
High Himalaya Frog Amphibia 352 XP_018413991.1 540 37.31%
Western clawed frog Amphibia 352 XP_012824143.1 657 32.70%
Yellowhead Catfish Osteichthyes 435 XP_027018543.1 577 26.93%
Whale Shark Chondrichthyes 473 XP_020385120.1 672 34.87%
Sea Vase Ascidiacea 676 XP_009860110.2 818 28.31%
Acorn Worm Hemichordata 684 XP_006811258.1 733 27.87%
Pacific Purple Sea Urchin Echinoidea 684 XP_011683370.1 791 23.76%
California two-spot octopus Mollusca 797 XP_014780749.1 689 27.05%
Mountainous Star Coral Cnidaria 824 XP_020617162.1 864 31.28%
Trichoplax Placozoa 948 XP_002117053.1 1247 34.84%
Sponge Porifera 952 XP_011405574.2 569 22.87%

Paralogs

There are no known paralogs of CCDC60.

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Protein interactions

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There are several binary protein interactions involving CCDC60 that have been experimentally verified.[21]

Interacting Proteins
Protein Function[22] Interaction
UPF3B Involved in nonsense-mediated decay (NMD) of mRNAs containing premature stop codons by associating with the nuclear exon junction complex (EJC) and serving as link between the EJC core and NMD machinery. Physical Association[23]
ZNF593 Negatively modulates the DNA binding activity of Oct-2 and therefore its transcriptional regulatory activity. Physical Association[23]
FAM32A Isoform 1, but not isoform 2 or isoform 3, may induce G2 arrest and apoptosis. Physical Association[23]
RBM42 Binds (via the RRM domain) to the 3'-untranslated region (UTR) of CDKN1A mRNA. Physical Association[23]
DCP1B May play a role in the degradation of mRNAs, both in normal mRNA turnover and in nonsense-mediated mRNA decay. Physical Association[23]
EGFR Receptor tyrosine kinase binding ligands of the EGF family and activating several signaling cascades to convert extracellular cues into appropriate cellular responses. Physical Association[24]
FAM204A Unknown function. Physical Association[23]
APP Functions as a cell surface receptor and performs physiological functions on the surface of neurons relevant to neurite growth, neuronal adhesion and axonogenesis. Direct Interaction[25]
MTUS2 Binds microtubules. Together with MAPRE1 may target the microtubule depolymerase KIF2C to the plus-end of microtubules. Direct Interaction[26]
B9D1 Component of the tectonic-like complex, a complex localized at the transition zone of primary cilia and acting as a barrier that prevents diffusion of transmembrane proteins between the cilia and plasma membranes. Direct Interaction[27]
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Clinical significance

Mutations in CCDC60 have been associated with decreased walking speed.[28] Additionally, CCDC60 is one of many candidate genes that has been associated with diagnosis of schizophrenia in genome-wide study.[29]

References

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