FAM203B

Family with Sequence Similarity 203, Member B (FAM203B) is a protein encoded by the FAM203B gene (8q24.3) in humans.[1][2] While FAM203B is only found in humans and possibly non-human primates, its paralog, FAM203A,[3] is highly conserved.[4] The FAM203B protein contains two conserved domains of unknown function, DUF383 and DUF384,[4] and no transmembrane domains.[5] This protein has no known function yet, although the homolog of FAM203A in Caenorhabditis elegans (Y54H5A.2) is thought to help regulate the actin cytoskeleton.[6]

HGH1
Identifiers
AliasesHGH1, BRP16, BRP16L, C8orf30A, C8orf30B, FAM203A, FAM203B, HGH1 homolog
External IDsMGI: 1930628 HomoloGene: 48742 GeneCards: HGH1
Gene location (Human)
Chr.Chromosome 8 (human)[7]
Band8q24.3Start144,137,769 bp[7]
End144,140,843 bp[7]
Orthologs
SpeciesHumanMouse
Entrez

51236

59053

Ensembl

ENSG00000235173

ENSMUSG00000022554

UniProt

Q9BTY7

Q8C3I8

RefSeq (mRNA)

NM_016458

NM_021555

RefSeq (protein)

NP_057542

NP_067530

Location (UCSC)Chr 8: 144.14 – 144.14 MbChr 15: 76.37 – 76.37 Mb
PubMed search[9][10]
Wikidata
View/Edit HumanView/Edit Mouse

Gene

FAM203B is located on the positive DNA strand of the long arm of chromosome 8 at locus 24.3 (8q24.3) from 76,368,898 - 76,371,411 in the human genome. The gene product contains 2,402 bp of mRNA with 6 predicted exons in the human gene.[2][11] There are no known isoforms.


FAM203B mRNA tissue expression levels.[12]

Gene Neighborhood

The pseudogene TSSK5P2 is located on the negative strand opposite FAM203B (145,440,975 - 145,443,775),[13] while LOC377711 is located immediately downstream on the positive strand (145,448,755 - 145,485,896).[14] FAM203A, MROH1, and SCXB are located upstream of FAM203B.[11][15]

Gene Expression

Expression Profile: mRNA expression has been localized in many tissue types (immune, nervous, muscle, internal, secretory, and reproductive) in similar quantities and may therefore be ubiquitous.[12]

Promoter: The predicted promoter region of FAM203B is located between 145,437,380 and 145,438,015 on Chromosome 8 and has a length of 636 bp.[16]


Protein

The function of FAM203B is not currently understood. The FAM203B protein has 390 amino acids,[1] a molecular weight of 42.1 kdal,[5] and an isoelectric point of 4.56.[17]

Structure

FAM203B contains two domains of unknown function: DUF383 (residues 110-288) and DUF384 (residues 292-349).[1] The protein is alanine-, proline-, and leucine-rich, but poor in serine, asparagine, threonine, isoleucine, lysine, and phenylalanine. The following internal repeats can be found in the primary sequence: LPFL (26-29, 245-248), ELAP (70-73), GRAL (54-57, 111-114), and LAADPGL (88-94, 99-105). There are no positive, negative, mixed charge, or hydrophobic clusters; no transmembrane domains; and no clusters of amino acid multiplets.[5] The secondary structure prediction generated by the Phyre 2.0 bioinformatic server shows only α-helices, almost all of which have high confidence values. The overall confidence value of the model is 99.5%.[18]

Post-Translational Modifications

There are at least six predicted phosphorylation sites in FAM203B: S17, S153, Y167, T223, S259, and S320.[19] The FAM203B protein is also predicted to locate to the cytoplasm.[20]

Protein Interactions

There are many possible transcription factor binding sites in the FAM203B promoter. Below is a table of the best possibilities, which have high confidence values, evolutionary conservation, and/or multiple possible binding sites in the promoter.[16]

Table of Possible Transcription Factor Binding Sites in Predicted FAM203B Promoter:[16]

Transcription FactorStartEndStrandSequence
Winged-helix transcription factor IL-2 enhancer binding factor, forkhead box K2622-gacaggacAACAcaggg
Hypermethylated in Cancer 14961+ccgTGCCagcctg
Zinc finger transcription factor ZBP-8994116+tggccactCCCCcattcagccct
Kidney-enriched kruppel-like factor, KLF15142158+gagccGGGGcgcgggcc
Transcription factor II B recognition element149155-ccgCGCC
Glial cells missing homolog 1, chorion-specific transcription factor GCMα159173+tcagaCCCTcagggc
Transcription factor AP-2α161175-gggcCCTGagggtct
Smad4 transcription factor involved in TGFβ signaling245255-gtaGTCTcggc
Nuclear factor 1278298-gatTTGGccgcctgccgcgtc
ZF5 POZ domain zinc finger, zinc finger protein 161295309+aatCGCGccgggcct
Smad3 transcription factor involved in TGFβ signaling365375-ggcGTCTggcc
Myeloid zinc finger protein MZF1384394-gcGGGGagtta
X-linked zinc finger protein397407+gcGGCCtggcc
Myeloid zinc finger protein MZF1406416-gaGGGGagggg
Core promoter-binding protein with 5 kruppel-type zinc fingers423445+ccggtcCCGCcccttgagcccag
X gene core promoter element 1424434-ggGCGGgaccg
Zinc finger and BTB domain-containing 7A479501-cgcaaCCCCgcccaccagaggag
Kruppel-like factor 7483499+tctggtgGGCGgggttg
Erythroid kruppel-like factor533549+ggcaccggtcGGGTggc
Hypermethylated in cancer 1541553-tgcTGCCacccga

There are several other proteins that may interact directly with the FAM203B protein including C1orf112, HEATR3, MRTO4, BYSL, GINS1, DKC1, TXNDC12, PWP2, IMP4, and NIP7.[21]

Predicted protein interactions with FAM203B, STRING 9.05.[21]

Homology and Evolution

FAM203A: Paralog

FAM203A is 99% identical to FAM203B with only one amino acid difference (E264Q) due to a point mutation (G857C).[1][15][22] This indicates that the duplication event that produced FAM203B 242,266 bp downstream[11] from FAM203A occurred very recently in evolutionary history. The FAM203A protein is highly conserved and has orthologs in primates, rodents, ungulates, marsupials, amphibians, fish, fungi, plants, and at least one monotreme, one reptile, and one hemichordate.[4][23]

Orthologs and Homologs

Table of FAM203B Paralog and Homologs:

Scientific NameCommon NameDivergence from Humans (MYA)[24]NCBI Protein AccessionGene NameProtein LengthSequence Similarity
Homo sapiensHuman0.0NP_057542FAM203A390100%
Macaca mulattaRhesus macaque29.2XM_001090013BRP16L39694%
Pan troglodytesChimpanzee6.3XP_520011FAM203A39598%
Mus musculusMouse92.3NP_067530FAM203A39386%
Sus scrofaWild boar94.2XP_003125495FAM203A-like40685%
Monodelphis domesticaGray short-tailed opossum162.6XP_003340757FAM203A-like48378%
Columba liviaRock dove296.0EMC87403BRP16 (partial)19464%
Danio rerioZebrafish400.1NP_001002522FAM203A37770%
Xenopus tropicalisWestern clawed frog371.2AAI60980LOC10014541237770%
Xenopus tropicalisWestern clawed frog371.2NP_001007916FAM203A35968%
Strongylocentrotus purpuratusPurple sea urchin742.9XP_793139FAM203A-like37262%
Anolis carolinensisCarolina anole301.7XP_003228921BRP16L28657%
Saccoglossus kowglevskiAcorn worm661.2XP_002739897BRP16L36261%
Danio rerioZebrafish400.1XP_002665502BRP16L18157%
Saccharomyces cerevisiaeBudding yeast1369.0NP_011703Hgh1p39452%
Arabidopsis thalianaThale cress1369.0NP_172882Armadillo/beta-catenin-like repeats-containing33949%

There is one ortholog of FAM203B, brain protein 16-like (BRP16L) in Macaca mulatta,[4][23] although no other primates appear to have orthologous proteins. There are two possible explanations for this anomaly: (1) DNA of other primates has not been sequenced thoroughly in the genomic region of the FAM203B ortholog, or (2) FAM203B is the result of a gene duplication event unique to humans, meaning that BRP16L in M. mulatta resulted from an earlier duplication event unique to that species. The second explanation is supported by the following evidence:

  1. Like M. mulatta, Danio rerio has both a FAM203A gene and a BRP16L gene. The large amount of time since the divergence of the M. mulatta and D. rerio lineages suggests that these BRP16L genes are the result of separate duplication events.
  2. The BRP16L protein in D. rerio has a significant 3’ truncation compared to the M. mulatta protein, further supporting the hypothesis that these proteins evolved separately.[22][25][26]
  3. If the BRP16L genes in "M mulatta" and "D. rerio" are the result of separate duplication events, then it is also possible that FAM203B and BRP16L in "M. mulatta" are the result of separate duplication events.
  4. BRP16 (brain protein 16) is an alias of FAM203A, and BRP16L (brain protein 16-like) is an alias of FAM203B. A gene named BRP16L simply means that the gene is related to FAM203A but not necessarily to FAM203B.
  5. FAM203A and FAM203B are located in the telomeric region of chromosome 8, an area of chromosomes that frequently experiences recombination events.

However, because FAM203A and FAM203B are so similar, it is difficult to determine whether proteins are orthologs or just simply homologs.

Unrooted phylogenetic tree showing the evolutionary relationships among FAM203B and its homologs.[22]

Phylogeny

The phylogenetic tree of FAM203B and its homologs matches with the overall divergence of the respective lineages.[22][24]

Conserved Domains, Motifs, and Residues

  1. ARM (armadillo/beta-catenin-like repeats-containing): Found in two homologs (FAM203A in Danio rerio and At1g14300 in Arabidopsis thaliana) and overlaps slightly with the beginning of the DUF383 domain. Related to the HEAT domain, consists of a 40-amino-acid tandemly repeated sequence motif, and is thought to mediate protein-protein interactions. Several eukaryotic genes contain ARM domains including armadillo in Drosophila melanogaster, beta-catenin, plakoglobin, and adenomatous polyposis coli in mammals.[4]
  2. DUF383: Domain of unknown function 383
  3. DUF384: Domain of unknown function 383
A schematic representation of the conserved domains in the FAM203B protein.

Every ortholog and homolog of FAM203B has a DUF383 domain and a DUF384 domain (except Anolis carolinensis, which is missing DUF384 due to a large 3' truncation[23][27]). There is significant variation among mammals, marsupials, and monotremes as to where the DUF383 domain begins, whereas this variation is smaller in reptiles, amphibians, fish, invertebrates, plants, and fungi. Additionally, the DUF383 domain ends at the same location for all homologs, while the DUF384 domain starts and ends at roughly the same location in all homologs. There is high homology in the DUF384 domain (292..349) and in the DUF383 domain (154..288), and several amino acids are completely conserved in vertebrates, invertebrates, plants, and fungi, which include Arg190, Gly219, Asn226, Lys273, and Lys338. Other highly conserved amino acids include Asn87, Lys88, Arg216, and Phe229.[4][22]

References

  1. 1 2 3 4 "Predicted: protein FAM203B [Homo sapiens]". NCBI Protein. Retrieved 5 February 2013.
  2. 1 2 "Predicted: Homo sapiens family with sequence similarity 203, member B (FAM203B, mRNA". NCBI Nucleotide. Retrieved 5 February 2013.
  3. ↑ "FAM203 family". NextProt Beta. Retrieved 5 February 2013.
  4. 1 2 3 4 5 6 "HomoloGene: 48742, gene conserved in Eukaryota". NCBI HomoloGene. Retrieved 18 January 2013.
  5. 1 2 3 Brendel, Volker. "SAPS (Statistical Analysis of PS)".
  6. ↑ Fievet BT, Rodriguez J, Naganathan S, Lee C, Zeiser E, Ishidate T, Shirayama M, Grill S, Ahringer J (January 2013). "Systematic genetic interaction screens uncover cell polarity regulators and functional redundancy". Nature Cell Biology. 15 (1): 103–12. doi:10.1038/ncb2639. PMC 3836181. PMID 23242217.
  7. 1 2 3 GRCh38: Ensembl release 89: ENSG00000235173 - Ensembl, May 2017
  8. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000022554 - Ensembl, May 2017
  9. ↑ "Human PubMed Reference:".
  10. ↑ "Mouse PubMed Reference:".
  11. 1 2 3 "FAM203B family with sequence similarity 203, member B [Homo sapiens (human)]". NCBI Gene. Retrieved 5 February 2013.
  12. 1 2 "FAM203B Gene". Weizmann Institute of Science. Retrieved 9 May 2013.
  13. ↑ "TSSK5P2 testis-specific serine kinase 5 pseudogene 2 [Homo sapiens (human)]". NCBI Gene. Retrieved 10 May 2013.
  14. ↑ "LOC377711 HEAT repeat-containing protein 7A-like [Homo sapiens (human)]". NCBI Gene. Retrieved 10 May 2013.
  15. 1 2 "FAM203A family with sequence similarity 203, member A [Homo sapiens (human)]". NCBI Gene. Retrieved 10 May 2013.
  16. 1 2 3 "Genomatix El Dorado". Retrieved 7 April 2013.
  17. ↑ Toldo, Luca. "PI (Isoelectric Point Determination)".
  18. ↑ Kelley LA, Sternberg MJ (2009). "Protein structure prediction on the Web: a case study using the Phyre server". Nature Protocols. 4 (3): 363–71. doi:10.1038/nprot.2009.2. PMID 19247286.
  19. ↑ Blom N, Gammeltoft S, Brunak S (December 1999). "Sequence and structure-based prediction of eukaryotic protein phosphorylation sites". Journal of Molecular Biology. 294 (5): 1351–62. doi:10.1006/jmbi.1999.3310. PMID 10600390.
  20. ↑ Horton, Paul. "PSORT II".
  21. 1 2 "C8orf30B Predicted Functional Partners". STRING: functional protein association networks. Retrieved 9 May 2013.
  22. 1 2 3 4 5 Higgins DG, Bleasby AJ, Fuchs R (April 1992). "CLUSTAL V: improved software for multiple sequence alignment". Computer Applications in the Biosciences. 8 (2): 189–91. doi:10.1093/bioinformatics/8.2.189. PMID 1591615.
  23. 1 2 3 "BLAST: Basic Local Alignment Search Tool". NCBI BLAST. Retrieved 5 February 2013.
  24. 1 2 Hedges SB, Dudley J, Kumar S (December 2006). "TimeTree: a public knowledge-base of divergence times among organisms". Bioinformatics. 22 (23): 2971–2. doi:10.1093/bioinformatics/btl505. PMID 17021158.
  25. ↑ "Predicted: brain protein 16-like [Macaca mulatta]". NCBI Protein. Retrieved 5 February 2013.
  26. ↑ "Predicted: brain protein 16-like [Danio rerio]". NCBI Protein. Retrieved 5 February 2013.
  27. ↑ "Predicted: brain protein 16-like [Anolis carolinensis]". NCBI Protein. Retrieved 10 May 2013.
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