CCDC138

Gene

The CCDC138 gene can be found at the positive strand of chromosome 2.[5]

Locus

The CCDC138 gene is located at the long(q) arm of chromosome 2 at locus 12.13,[6] or in short 2q12.3. It can be found at location 108,786,752-108,876,591.[7] The DNA sequence is 89,840bp long.

The red line shows the CCDC138 locus on chromosome 2q12.3.

Common aliases

CCDC138 is the only established common alias.

Homology and evolution

Paralogs

No paralogs of CCDC138 have been identified.

Orthologs

CCDC138 is conserved in various organisms as shown in the table below.

Scientific nameCommon nameDate of divergence from human lineage[8]Sequence lengthSequence identity to human RNA/proteinSequence similarity to human RNA/protein
Mus musculusHouse mouse92.3 MYA2466 bp77%65.7%
Columbia liviaRock dove296 MYA1863 bp61%59.4%
Xenopus laevisAfrican clawed frog371.2 MYA2634 bp52%40.1%
Anolis carolinensisRed-throated anole296 MYA9588 bp78%46.3%
Latimeria chalumnaeWest Indian Ocean coelacanth414.9 MYA1838 bp71%38.1%
Strongylocentrotus purpuratusPurple sea urchin742.9 MYA2047 bp59%14.5%
Ciona intestinalisVase tunicate722.5 MYA2420 bp56%23.8%
Aplysia californicaCalifornia sea slug782.7 MYA2103 bp49%17.2%
Hydra vulgarisFresh-water polyp855.3 MYA1482 bp46%13.7%
Chrysemys picta belliiWestern painted turtle296 MYA700 bp36%15.9%
Alligator mississippiensisAmerican alligator296 MYA2089 bp76%38.4%
Melopsittacus undulatusBudgerigar296 MYA1764 bp73%40.3%
Taeniopygia guttataZebra finch296 MYA1980 bp75%44.2%
Lepisosteus oculatusSpotted gar400.1 MYA1269 bp65%30.9%
Saccoglossus kowalevskiiAcorn worm661.2 MYA2515 bp42%24.1%
Branchiostoma floridaeLancelet713.2 YA1758 bp55%27.0%
Maylandia zebraZebra mbuna fish400.1 MYA4815 bp58%21.4%
Trichoplax adhaerensTrichoplax800 MYA1605 bp56%10.3%
Pelodiscus sinensisChinese softshell turtle296 MYA2895 bp77%33.9%
Falco cherrugSaker falcon296 MYA1866 bp73%48.9%

Distant homologs

The most distant homolog detected or predicted is Trichoplax adhaerans. It has a conserved CCDC138 gene and has evolved 800 MYA before the human lineage.

Homologous domains

Among the orthologs stated above, there are various homologous regions that are conserved shown in figures below.

CCDC138 multiple sequence alignment showing conserved regions.
CCDC138 multiple sequence alignment showing conserved regions.
CCDC138 multiple sequence alignment showing conserved regions.

Green colors shows completely conserved residues, yellow color shows identical residues, cyan color shows similar residues, white color shows different residues.

Phylogeny

The observed phylogeny of the CCDC138 gene of the above mentioned orthologs recapitulates the evolutionary history.[9]

CCDC138 rooted phylogeny tree

The figure above shows the evolutionary relationship of CCDC138 in the orthologs.

Protein

The CCDC138 protein is predated to have a molecular weight of 76.2Kda[10] and an isoelectric point of 8.614.[11] Compositional analysis shows that there is a low usage of the AGP grouping in CCDC138, and there are no positive, negative or mixed charge clusters. The protein has no ER retention motif in the C-terminus and no RNA binding motif.[12] It has also been predicted to be a soluble nuclear protein with a leucine zipper pattern (PS00029) at position 205 onwards with a sequence LQKRERFLLEREQLLFRHENAL.[12]

Primary sequence and variants/isoforms

There are two isoforms of the CCDC138 protein. The primary isoform has 665 amino acids[13] while the secondary isoform has 577 amino acids,[13] and is missing 88 amino acids at the C-terminus.

Pairwise sequence alignment comparing isoforms 1 and 2 of the CCDC138 protein.

Figure shows the pairwise sequence alignment comparing the primary isoform (Isoform 1) to the secondary isoform (Isoform 2).

Domain and motifs

A domain of unknown function (DUF2317) on the protein at location 212 – 315 has been characterized in bacteria. TMHMM[14] and TMAP[15] suggests that there are no predicted transmembrane domain. SOSUI[16] further predicts that CCDC138 is a soluble protein with no transmembrane domain.

Post-translational modifications

According to SUMOplot Analysis Program,[17] there are 7 predicted sumoylation at lysine residues K7, K207, K336, K374, K383, K521, and K591. NetPhos[18] predicts that there are 44 phosphorylations sites, including 29 serine residues, 10 threonine residues, and 5 tyrosine residues. There are no further post-translational modifications as predicted by NetNGlyc,[19] NetOGlyc,[20] SignalP,[21] Sulfinator,[22] and Myristoylator.[23]

Secondary structure

The CCDC138 protein contains multiple alpha helixes, beta sheets and coiled-coils as predicted by PELE, CHOFAS, and GOR4.

CCDC138 secondary structure as predicted by PELE

Yellow shows coiled-coil, blue shows alpha helix, and red shows beta sheet. The majority of the sequence are coiled-coils and alpha helixes.

3° and 4° structures

There are no predicted 3° and 4° Structures for the CCDC138 protein. However, there is a similar structure that has a 29% identity.[24] The predicted structure is Chain A, crystal structure analysis of Clpb, a protein that encodes an ATP-dependent protease and chaperone. This protein has an aligned-length of 144 amino acids, and the alignment is located at the domain of unknown function of CCDC138.

Chain A, crystal analysis structure of Clpb

Expression

The gene is expressed at low levels in almost all human tissues, but higher levels have been seen in certain cancer tissues. CCDC138 is a soluble protein that is pre diced to localise in the nucleus of a cell.

Promoter

The promoter region of CCDC138 is shown as figure below.

Promoter region of CCDC138 with labeled transcription factor binding sites

Expression

Microarray-assessed tissue expression patterns through GEO profiles show that CCDC138 is expressed in moderate levels in various tissues including peripheral blood lymphocyte, fetal thymus, thymus, testis, ovary, feral brain, colon, mammary gland, and bone marrow.[25]

Microarray-assessed tissue expression patterns shown in GEO profile.

Transcript variants

There are two most significant alternative transcript variants for CCDC138 mRNA. The first variant as shown in the figure below has been found in lung, blood, and human embryonic stem cells.[26] The second variant has been found in adenocarcinoma, prostate, lung, and primary lung epithelial cells.[27]

Transcript variants of CCDC138

First transcript shows the complete mRNA transcript. Second transcript is the first variant, while the thirst transcript is the second variant.[28]

Function and biochemistry

The exact function of CCDC138 is yet to be known.

Interacting proteins

The CCDC138 protein has been found to interact with ubiquitin C,[29] a protein involved in ubiquination and eventually protein degradation.

Transcription factors that might bind to regulatory sequence

The table below shows some transcription factors that have been predicted by Genomatix that binds to the regulatory sequence of the CCDC138 gene.[30]

Detailed family informationDetailed matrix informationTissue
GC-Box factors SP1/GCStimulating protein 1, ubiquitous zinc finger transcription factorUbiquitous
Peroxisome proliferator-activated receptorPeroxisome proliferator-activated receptor gamma, DR1 sitesAdipose Tissue, Connective Tissue, Digestive System, Liver
MYT1 C2HC zinc finger proteinMyT1 zinc finger transcription factor involved in primary neurogenesisCentral Nervous System, Nervous System, Neuroglia, Neurons
NGFI-B response elements, nur subfamily of nuclear receptorsMonomers of the nur subfamily of nuclear receptors (nur77, nurr1, nor-1)Brain, Central Nervous System, Endocrine System, Immune System, Leydig Cells, Nervous System, Neurons, Testis, Thymus Gland, Urogenital System
Krueppel-like transcription factorsCore promoter-binding protein (CPBP) with 3 Krueppel-type zinc fingers (KLF6, ZF9)Blood cells, bone marrow cells, digestive system, embryonic structures, Erythrocytes, Hematopoietic System, liver
Grainyhead-like transcription factorsGrainyhead-like 3 (sister-of-mammalian grainyhead - SOM)Embryonic Structures, Integumentary System
CTCF and BORIS gene family, transcriptional regulators with 11 highly conserved zinc finger domainsInsulator protein CTCF (CCCTC-binding factor)Blood Cells, Embryonic Structures, Endocrine System, Erythrocytes, Germ Cells, Testis, Urogenital System
Core promoter motif ten elementsHuman motif ten element-
Abdominal-B type homeodomain transcription factorsHomeobox C13 / Hox-3gammaBone Marrow Cells, Bone and Bones, Central Nervous System, Connective Tissue, Embryonic Structures, Hematopoietic System, Integumentary System, Kidney, Nervous System, Neurons, Prostate, Skeleton, Spinal Cord, Urogenital System
E2F-myc activator/cell cycle regulatorE2F transcription factor 2Ubiquitous
PAX-3 binding sitesPax-3 paired domain protein, expressed in embryogenesis, mutations correlate to Waardenburg SyndromeEmbryonic structures, muscle, skeletal, muscles
ZF5 POZ domain zinc fingerZF5 POZ domain zinc finger, zinc finger protein 161-
Vertebrate TATA binding protein factorCellular and viral TATA box elements-
CCAAT binding factorsAvian C-type LTR CCAAT boxUbiquitous
Ccaat/Enhancer Binding ProteinCCAAT/enhancer binding protein alphaAdipose Tissue, Bone Marrow Cells, Connective Tissue, Digestive System, Hematopoietic System, Immune System, Liver, Myeloid Cells, Phagocytes
Activator-, mediator- and TBP-dependent core promoter element for RNA polymerase II transcription from TATA-less promotersX gene core promoter element 1-

Clinical significance

CCDC138 has been identified as one of the many genes involved in initiating term labor in myometrium.[31]

References

  1. GRCh38: Ensembl release 89: ENSG00000163006 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000038010 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Homo sapiens coiled-coil domain containing 138 (CCDC138), mRNA". Retrieved 2 Feb 2014.
  6. "CCDC138 - GeneCards". Retrieved 2 Feb 2014.
  7. "CCDC138 coiled-coil domain containing 138 [ Homo sapiens (human) ]". Retrieved 2 Feb 2014.
  8. "TimeTree :: The Timescale of Life". Retrieved 5 March 2014.
  9. "CLUSTALW". Retrieved 1 March 2014.
  10. "SAPS". Retrieved 10 April 2014.
  11. "pI". Retrieved 10 April 2014.
  12. "PSORT WWW Server". Retrieved 18 April 2014.
  13. "Coiled-coil domain-containing protein 138 - CCDC138 - Homo sapiens (Human)". Retrieved 10 February 2014.
  14. "TMHMM". Retrieved 20 April 2014.
  15. "TMAP". Retrieved 20 April 2014.
  16. "Classification and Secondary Structure Prediction of Membrane Proteins". Retrieved 15 April 2014.
  17. "SUMOplot™ Analysis Program". Retrieved 15 April 2014.
  18. "NetPhos 2.0 Server". Retrieved 15 April 2014.
  19. "NetNGlyc 1.0 Server". Retrieved 15 April 2014.
  20. "NetOGlyc 4.0 Server". Retrieved 15 April 2014.
  21. "SignalP 4.1 Server". Retrieved 15 April 2014.
  22. "The Sulfinator". Retrieved 15 April 2014.
  23. "Myristoylator". Retrieved 15 April 2014.
  24. "CBLAST". Retrieved 22 April 2014.
  25. "GDS3113 / 172084 / CCDC138". Retrieved 29 March 2014.
  26. "AHomo sapiens coiled-coil domain containing 138 (65.7 kD) (CCDC138) alternative variant dAug10, complete mRNA". Retrieved 30 March 2014.
  27. "Homo sapiens coiled-coil domain containing 138 (47.0 kD) (CCDC138) alternative variant fAug10, complete mRNA". Retrieved 30 March 2014.
  28. "AceView: Gene:CCDC138, a Comprehensive Annotation of Human, Mouse and Worm Genes with mRNAs or ESTs". Retrieved 30 March 2014.
  29. "CCDC138 protein (Homo sapiens) - STRING network view". Retrieved 22 April 2014.
  30. "Transcription Factors". Retrieved 27 March 2014.
  31. Weiner CP, Mason CW, Dong Y, Buhimschi IA, Swaan PW, Buhimschi CS (May 2010). "Human effector/initiator gene sets that regulate myometrial contractility during term and preterm labor". American Journal of Obstetrics and Gynecology. 202 (5): 474.e1–20. doi:10.1016/j.ajog.2010.02.034. PMC 2867841. PMID 20452493.
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