C8orf48

Last updated
C8orf48
Identifiers
Aliases C8orf48 , chromosome 8 open reading frame 48
External IDs MGI: 2142538 HomoloGene: 82747 GeneCards: C8orf48
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001007090

NM_001039220

RefSeq (protein)

NP_001007091

NP_001034309

Location (UCSC) Chr 8: 13.57 – 13.57 Mb Chr 8: 37.46 – 37.46 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

C8orf48 is a protein that in humans is encoded by the C8orf48 gene. [5] C8orf48 is a nuclear protein specifically predicted to be located in the nuclear lamina. [6] [7] C8orf48 has been found to interact with proteins that are involved in the regulation of various cellular responses like gene expression, protein secretion, cell proliferation, and inflammatory responses. [8] [9] [10] This protein has been linked to breast cancer and papillary thyroid carcinoma. [11] [12]

Contents

Gene

C8orf48 is located on chromosome 8 (8p22) and spans from 13,566,843 to 13,568,288 on the positive strand. [13] C8orf48 has an exon count of 1 and no introns. [5] [14] This protein does not have any isoforms nor exhibit any alternative splicing.

Protein

The protein C8orf48 is 319 amino acids in length. [15] The molecular weight of this protein is 36.9 kDa and the isoelectric point is 8.86. [16] The C8orf48 protein is predicted to be a nuclear protein particularly located in the nuclear lamina. [6] This protein does not possess any signal peptides or transmembrane domains. This protein has also been found to be fairly abundant in humans. [17]

Structure

C8ORF48 Primary Structure.jpg

C8orf48 protein has two predicted nuclear localization signals one spanning from 135-149 amino acids and the other from 204-221. [7] The secondary structure of C8orf48 protein is composed of primarily alpha-helices and coiled coils. The structure is composed of very little beta sheets, a total of three areas demonstrate possible beta sheet structure. [16]

The Tertiary structure of C8orf48 was obtained from the iTASSER program.

ITasser Predicted C8ORF48 Tertiary Structure .png

Post-translational modifications

C8orf48 has various predicted post-translational modifications. These post-translational modifications include O-glycosylation, Glycation, N-linked glycosylation, Phosphorylation Sites, Yin-Yang sites, sumoylation, and SUMO interactions. [19]

Subcellular localization

PSORT II results determined that the protein C8orf48 does not have a signalPeptide as well as no transmembrane domains. [20] The prediction is that C8orf48 is most likely nuclear and potentially cytoplasmic. When comparing orthologs of C8orf48 we see very similar results, the protein is predicted to be localized in the nucleus predominantly and secondly predicted to be localized in the cytoplasm. Further sub-cellular localization analysis was done through the use of CELLO. [21] These results also support the notion that C8orf48 is localized in the nucleus.

Homology

Phylogenetic Tree of C8orf48 (Unrooted) Phylogenetic Tree of C8ORF48 (Unrooted).jpg
Phylogenetic Tree of C8orf48 (Unrooted)

C8orf48 is conserved in mammals, amphibians, reptiles, aves, and fish. [22] C8orf48 orthologs were unable to be found in bacteria, archea, plants, and fungi. [22] There were no human paralogs found of C8orf48. Certain portions of the DUF 4606 domain is highly conserved in the orthologs.

Expression

This gene has been found to be overly expressed in the tissues of the testis and colon muscle, as well as expressed in 76 developmental stages. [23] C8orf48 has been found to be expressed most often in the bladder, bone, heart, larynx, testis, and thyroid. [24] In regards to the developmental stages, C8orf48 was most often found in the embroid body. [24]

PaxDB C8ORF48 Protein Abundance.png

GEO profiles

Differential Tissue Expression of C8orf48 Overall Expression GEO.png
Differential Tissue Expression of C8orf48

In a study regarding multiple myeloma bone marrow mesenchymal stromal cells shows that the expression of C8orf48 is lower in the disease state cells in comparison to healthy cells. [25] the opposite is demonstrated in the GeoProfile regarding Endometriosis, in this study, it was found that C8orf48 levels are higher in the disease state than in the healthy state. [26] Other studies demonstrate differential expression of Papillary Thyroid cancer and Estrogen Receptor alpha-silenced MCF7 breast cancer cells. In control samples the levels of C8orf48 were lower than that of those with the Estrogen receptor knockdown. [11]

Regulation of expression

The transcription factors that act on C8orf48 are presented in Table 1. The majority of the transcription factors are involved in cell growth, proliferation, or regulation of cell migration. This implies that C8orf48 may play a role in the cell cycle. A few of the transcription factors presented themselves more than once, on both the positive and negative strand. These transcription factors include MAX binding protein and Estrogen-related receptor alpha (secondary DNA binding preference) both of which are involved in cell growth. [27] [28]

Transcription FactorFunction
Myeloid zinc finger protein MZF1Found to be expressed in hematopoietic progenitor cells that are committed to myeloid lineage differentiation. It contains 13 C2H2 zinc fingers arranged in two domains that are separated by a short glycine- and proline-rich sequence. [29]
Zinc finger with KRAB and SCAN domains 3It is mainly located in the nucleus although during starvation periods it relocates to the cytoplasm. This allows for expression of target genes involved in autophagy and lysosome biogenesis/function. Acts as a repressor of autophagy and has been found and promote cancer cell progression and/or migration in various tumors and myelomas. [30]
T-box transcription factor TBX20Found to be involved in the regulation of a genetic program for cranial motor neuron cell body migration. [31]
Kruppel-like zinc finger protein 219Found to be involved in the regulation of chondrocyte differentiation by assembling a transcription factory with Sox9. [32]
KRAB-containing zinc finger protein 300Research links the transcriptional repression mediated by the KRAB-ZFPs to cell proliferation, differentiation, apoptosis and cancer. Believed to have evolved recently. [33]
Krueppel-like factor 2 (lung) (LKLF)KLF2 regulates T-cell trafficking by promoting the expression of S1P1 that is a lipid-binding receptor. This transcription factor binds to the CACCC box in the promoter sequence. [34]
Estrogen-related receptor alpha (secondary DNA binding preference)The expression of this has been shown to have a negative prognostic significance in breast and ovarian cancers. Said to be critical for the growth of Estrogen receptor negative breast cancer. [28]
AREB6 (Atp1a1 regulatory element binding factor 6)AREB6’s structure is composed of two zinc-finger clusters in N- and C-terminal regions, and one homeodomain in the middle. It has been found to regulate the expression of the Na, K-ATPase α1 subunit, interleukin 2 and δ-crystallin genes. [35]
MAX binding proteinTranscriptional repressor and an antagonist of Myc-dependent transcriptional activation and cell growth. [27]
Leucine rich repeat (in FLII) interacting protein 1A transcriptional repressor that potentially regulates TNF, EGFR and PDGFA. Possibly involved in the control of smooth muscle cell proliferation following artery injury. [36]
E2F transcription factor 1Plays an important role in the control of the cell cycle and tumor suppressor proteins. Also found to be the target of transforming proteins of small DNA tumor viruses. Lastly, it can mediate cell proliferation and p53-dependent/independent apoptosis. [37]
Kruppel-like factor 7 (ubiquitous, UKLF)Members of the family it pertains to are responsible for the regulation of cell proliferation, differentiation, and survival. Found to possibly contribute to the progression of type 2 diabetes by inhibiting the expression of insulin, secretion in pancreatic beta-cells, and by deregulating adipocytokine secretion in adipocytes. [38]
CCAAT/enhancer binding protein (C/EBP), epsilonImportant for terminal differentiation and functional maturation of committed granulocyte progenitor cells. Mutations in the gene that encodes this protein has been found to be associated with Specific Granule Deficiency. [39]
Zinc finger / POZ domain transcription factorThe POZ domain is a conserved protein-protein interaction motif found in transcription factors, oncogenic proteins, ion channel proteins, and some actin-associated proteins. [40]
Oligodendrocyte lineage transcription factor 2Tends to be expressed in oligodendrocyte tumors in the brain. This protein is an essential regulator of ventral neuroectodermal progenitor cell fate and chromosomal translocation t(14;21)(q11.2;q22) associated with T-cell acute lymphoblastic leukemia. [41]
Basic krueppel-like factor (KLF3)One of its related pathways is transcriptional regulation in cancer, and may possibly have a role in hematopoiesis. Binds to the CACCC box of erythroid cell-expressed genes. [42]

Protein interactions

The proteins that interact with C8orf48 include Deleted In Liver Cancer 1 Protein (DLC1), MyoD Family Inhibitor (MDFI), Zinc Finger Protein 14 (ZNF14), and Sacroglycan Zeta (SGCZ). [8] All of these protein interactions were found experimentally via a two-hybrid pooling approach, two-hybrid array, or two-hybrid screen. [10]

Clinical significance

C8orf48 has been found in studies regarding various types of carcinoma. Different C8orf48 expression levels have been found in Papillary Thyroid cancer and Estrogen Receptor alpha-silenced MCF7 breast cancer cells. [25] [26]

Related Research Articles

ANKRD24

Ankyrin repeat domain-containing protein 24 is a protein in humans that is coded for by the ANKRD24 gene. The gene is also known as KIAA1981. The protein's function in humans is currently unknown. ANKRD24 is in the protein family that contains ankyrin-repeat domains.

TMEM156 is a gene that encodes the transmembrane protein 156 (TMEM156) in Homo sapiens. It has the clone name of FLJ23235.

Chromosome 16 open reading frame 95 (C16orf95) is a gene which in humans encodes the protein C16orf95. It has orthologs in mammals, and is expressed at a low level in many tissues. C16orf95 evolves quickly compared to other proteins.

PRR29

PRR29 is a protein located on human chromosome 17 that in humans is encoded by the PRR29 gene.

Coiled-coil domain containing protein 180 (CCDC180) is a protein that in humans is encoded by the CCDC180 gene. This protein is known to localize to the nucleus and is thought to be involved in regulation of transcription as are many proteins containing coiled-coil domains. As it is expressed most highly in the testes and is regulated by SRY and SOX transcription factors, it could be involved in sex determination.

Uncharacterized protein Chromosome 16 Open Reading Frame 71 is a protein in humans, encoded by the C16orf71 gene. The gene is expressed in epithelial tissue of the respiratory system, adipose tissue, and the testes. Predicted associated biological processes of the gene include regulation of the cell cycle, cell proliferation, apoptosis, and cell differentiation in those tissue types. 1357 bp of the gene are antisense to spliced genes ZNF500 and ANKS3, indicating the possibility of regulated alternate expression.

Cardiac-enriched FHL2-interacting protein (CEFIP) is a protein encoded by the gene C10orf71 on chromosome 10 open reading frame 71. It is primarily understood that this gene is moderately expressed in muscle tissue and cardiac tissue.

C12orf60

Uncharacterized protein C12orf60 is a protein that in humans is encoded by the C12orf60 gene. The gene is also known as LOC144608 or MGC47869. The protein lacks transmembrane domains and helices, but it is rich in alpha-helices. It is predicted to localize in the nucleus.

C2orf73

Uncharacterized protein C2orf73 is a protein that in humans is encoded by the C2orf73 gene. The protein is predicted to be localized to the nucleus.

C15orf39

C15orf39 is a protein that in humans is encoded by the Chromosome 15 open reading frame 15 (C15orf39) gene.

C16orf86

Uncharacterized protein C16orf86 is a protein in humans that is encoded by the C16orf86 gene. It is mostly made of alpha helices and it is expressed in the testes, but also in other tissues such as the kidney, colon, brain, fat, spleen, and liver. For the function of C16orf86, it is not well understood, however it could be a transcription factor in the nucleus that regulates G0/G1 in the cell cycle for tissues such as the kidney, brain, and skeletal muscles as mentioned in the DNA microarray data below in the gene level regulation section.

CFAP299 Protein-coding gene in the species Homo sapiens

Cilia- and flagella-associated protein 299 (CFAP299), is a protein that in humans is encoded by the CFAP299 gene. CFAP299 is predicted to play a role in spermatogenesis and cell apoptosis.

C7orf26 Human protein-encoding gene on chromosome 7

c7orf26 is a gene in humans that encodes a protein known as c7orf26. Based on properties of c7orf26 and its conservation over a long period of time, its suggested function is targeted for the cytoplasm and it is predicted to play a role in regulating transcription.

SMCO3

Single-pass membrane and coiled-coil domain-containing protein 3 is a protein that is encoded in humans by the SMCO3 gene.

TEDC2

Tubulin epsilon and delta complex 2 (TEDC2), also known as Chromosome 16 open reading frame 59 (C16orf59), is a protein that in humans is encoded by the TEDC2 gene. Its NCBI accession number is NP_079384.2.

C20orf202

C20orf202 is a protein that in humans is encoded by the C20orf202 gene. In humans, this gene encodes for a nuclear protein that is primarily expressed in the lung and placenta.

C1orf94 Protein-coding gene in the species Homo sapiens

Chromosome 1 Opening Reading Frame 94 or C1orf94 is a protein in human coded by the C1orf94 gene. The function of this protein is still poorly understood.

C12orf24

C12orf24 is a gene in humans that encodes a protein known as FAM216A. This gene is primarily expressed in the testis and brain, but has constitutive expression in 25 other tissues. FAM216A is an intracellular protein that has been predicted to reside within the nucleus of cells. The exact function of C12orf24 is unknown. FAM216A is highly expressed in Sertoli cells of the testis as well as different stage spermatids.

C6orf136

C6orf136 is a protein in humans encoded by the C6orf136 gene. The gene is conserved in mammals, mollusks, as well some porifera. While the function of the gene is currently unknown, C6orf136 has been shown to be hypermethylated in response to FOXM1 expression in Head Neck Squamous Cell Carcinoma (HNSCC) tissue cells. Additionally, elevated expression of C6orf136 has been associated with improved survival rates in patients with bladder cancer. C6orf136 has three known isoforms.

C5orf22

Chromosome 5 open reading frame 22 (c5orf22) is a protein-coding gene of poorly characterized function in Homo sapiens. The primary alias is unknown protein family 0489 (UPF0489).

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