FAM114A1
| FAM114A1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Aliases | FAM114A1, Noxp20, family with sequence similarity 114 member A1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | MGI: 1915553 HomoloGene: 12259 GeneCards: FAM114A1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Protein FAM114A1 also known as nervous system overexpressed protein 20 (NOXP20) is a protein that in humans is encoded by the FAM114A1 gene.[4] Orthologs of FAM114A1 can be found in organisms as taxonomically distant from Homo sapiens as Drosophila. However, as expected, human FAM114A! is more like that of primates than any other orthologs. FAM114A1 has one paralog, FAM114A2, which also encodes a protein of unknown function.
Gene
FAM114A1 is located on the short arm of Chromosome 4 (4.p14) in humans on the forward strand sense, it starts at base pair 38869354 and ends at 38947365.[4] Its mRNA has 4138 bp. The gene has the following neighbors on the same chromosome:
- TLR1: Toll-like receptor (TLR) 1 plays a role in pathogen recognition and activation of innate immunity.
- TLR6: Toll-like receptor (TLR) 6 plays a role in pathogen recognition and activation of innate immunity.
- TMEM156: The gene codes for a transmembrane protein.
- KLHL5: Kelch-like 5, its protein is thought to have a role in lymphocyte activation.[5]
Homology
| Genus and species | Common name | Accession number | Seq. length | Seq. identity | Seq. similarity |
| Pan troglodytes | Chimpanzee | XP_517149.2 | 563 a | 99% | 99% |
| Macaca mulatta | Rhesus macaque | EHH25809.1 | 563 a | 97% | 98% |
| Nomascus leucogenys | Northern white-cheeked gibbon | XP_003258632.1 | 562 a | 97% | 98% |
| Macaca fascicularis | Crab-eating macaque | EHH53615.1 | 563 a | 96% | 98% |
| Pongo abelii | Sumatran orangutan | XP_002814719.1 | 563 a | 98% | 96% |
| Equus caballus | Horse | XP_001498667.1 | 562 a | 88% | 93% |
| Loxodonta africana | African bush elephant | XP_003411349.1 | 558 a | 85% | 91% |
| Heterocephalus glaber | Naked mole rat | EHB16215.1 | 561 a | 86% | 90% |
| Cavia porcellus | Guinea pig | XP_003471670.1 | 569 a | 86% | 90% |
| Bos taurus | Cow | XP_588946.3 | 563 a | 84% | 90% |
| Sus scrofa | Wild boar | XP_003128969.1 | 562 a | 84% | 90% |
| Ailuropoda melanoleuca | Giant panda | XP_002928170.1 | 570 a | 83% | 89% |
| Canis lupus familiaris | Dog | XP_536261.3 | 560 a | 83% | 88% |
| Rattus norvegicus | Rat | XP_573600.2 | 567 a | 78% | 83% |
| Mus musculus | Mouse | BAB30694.1 | 569 a | 77% | 83% |
| Monodelphis domestica | Gray short-tailed opossum | XP_001374188.1 | 562 a | 72% | 81% |
| Meleagris gallopavo | Wild turkey | XP_003205919.1 | 563 a | 64% | 76% |
| Gallus gallus | Chicken | XP_423859.3 | 561 a | 64% | 75% |
| Taeniopygia guttata | Zebra finch | XP_002189709.1 | 565 a | 61% | 75% |
| Anolis carolinensis | Carolina anole | XP_003226293.1 | 539 a | 61% | 75% |
| Danio rerio | Zebra fish | NP_001082947.1 | 546 a | 57% | 72% |
| Xenopus (silurana) tropicalis | Western clawed frog | XP_002938704.1 | 424 a | 66% | 79% |
Expression
NOXP20 is over-expressed in the brain,[6] microarray data [7] using the Allen Brain Atlas provides evidence of that expression. Data from NCBI GEO Profile [8] shows that although FAM114A1 is expressed in the brain, its expression goes beyond the nervous tissue to include most of the tissue types in the human body. GEO Profiles also show that FAM114A1 is more expressed in mesenchyme stem cells than in undifferentiated stem cells. Further experiments [8] have shown that there are certain factors that affect the expression of FAM114A1. One example is the direct relation between the over-expression of CLDN-1 and the over-expression of FAM114A1.
Protein
NOXP20 is made up of 563 amino acids and weighs 60742 Da with an iso-electric point of 4.415999. Little is known about the details of this protein, however, there is a good deal of scientific predictions for the protein's structure and function. Like any other protein, this protein undergoes post-translational modifications. The modification that has been proven to be true is phosphorylation on two of the protein's amino acids 196 and 199.
Structure
There are several tools available to predict the secondary structure of a protein. One tool that combines the results of few of them is PELE on SDSC Biology WorkBench.[9] According to this tool, the protein's secondary structure is mostly alpha helices and coils with some beta strands around the structure.
Interactions
There is not proof of any interactions that the FAM114A1 protein has with other proteins in the human body. However, an interaction between FAM114A1 and CDGSH iron sulfur domain 2 was detected in mice.[10] There is 77% identity and 83% similarity between the amino acids of NOXP20 in the two species (Homo sapiens and Mus musculus). Due to the close relation between the two species we can assume that NOXP20 has the same interaction in humans.
Function
The exact function of NOXP20 is still not well understood. However, there has been evidence that the protein carries a caspase recruiting domain on it.[6] Knowing that caspase is involved in apoptosis, this information leads us to believe that NOXP20 could have a role in apoptosis and regulation of cell proliferation.
References
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000029185 – Ensembl, May 2017
- ^ "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.
- ^ a b "FAM114A1 family with sequence similarity 114, member A1 [Homo sapiens]". NCBI. Retrieved 22 April 2012.
- ^ "GeneCards". Genecards. Retrieved 28 April 2012.
- ^ a b Boucquey M, De Plaen E, Locker M, Poliard A, Mouillet-Richard S, Boon T, Kellermann O (Oct 2006). "Noxp20 and Noxp70, two new markers of early neuronal differentiation, detected in teratocarcinoma-derived neuroectodermic precursor cells". Journal of Neurochemistry. 99 (2): 657–69. doi:10.1111/j.1471-4159.2006.04093.x. PMID 17029606.
- ^ "Micro-Array Data". Allen Institute for Brain Science. Retrieved 28 April 2012.
- ^ a b "Geo Profiles". NCBI. Retrieved 28 April 2012.
- ^ "Biology Workbench". SDSC Biology WorkBench. Retrieved 28 April 2012.
- ^ "String". STRING9.0. Retrieved 28 April 2012.
Further reading
- Boucquey M, De Plaen E, Locker M, Poliard A, Mouillet-Richard S, Boon T, Kellermann O (Oct 2006). "Noxp20 and Noxp70, two new markers of early neuronal differentiation, detected in teratocarcinoma-derived neuroectodermic precursor cells". Journal of Neurochemistry. 99 (2): 657–69. doi:10.1111/j.1471-4159.2006.04093.x. PMID 17029606.