Fam78b

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

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RefSeq (protein)

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Family with Sequence Similarity 78-Member B (FAM78B) is a protein of unknown function in humans that is encoded by the FAM78B gene (1q24.1). It has orthologous genes and predicted proteins in vertebrates and several invertebrates, but not in arthropods. It has a nuclear localization signal in the protein sequence and a miRNA target region of the mRNA sequence.

Evolutionary analysis

Homology

FAM78B has one paralog, FAM78A, and is conserved throughout many species. Orthologs can be found throughout all vertebrates excluding arthropods. FAM78B is also found in several invertebrates including the pacific oyster and liver fluke. FAM78A, it’s paralog, is also found to be conserved in more invertebrates such as the tunicates, worms, and leeches, and make up the distant homologs of FAM78B. The table below contains a list of FAM78B orthologs with percent identity values and time since divergence values relative to the human FAM78B gene or protein.[1]

File:FAM78B-Evolutionary-History-Graph1.png
Evolutionary History of FAM78B comparing percent identity versus time (millions of years)
Genus and species Common name Date of divergence from

human lineage (millions of years ago)

Accession number Sequence length (bp or aa) Protein/mRNA identity (%) Query cover (%)
Crassostrea gigas Pacific oyster 782.7 EKC28338.1 267 48 79
Clonorchis sinensis Liver fluke 792.4 GAA32739.1 295 33 84
Xiphophorus maculatus Platyfish 400.1 XP_005802428.1 285 80 100
Takifugu rubripes Pufferfish 400.1 XP_003975800.1 261 80 100
Danio rerio Zebrafish 400.1 XP_001338241.2 285 80 100
Lepisosteus oculatus Spotted gar 400.1 XP_006635127.1 261 90 100
Xenopus (Silurana) tropicalis Western clawed frog 371.2 XP_002933818.1 263 93 100
Alligator mississippiensis Alligator 296 XP_006276782.1 261 92 100
Anolis carolinensis Anole lizard 296 XP_003219922.1 261 90 100
Gallus gallus Chicken 296 XP_001232254.1 261 90 100
Pseudopodoces humilis Groundpecker 296 XP_005528713.1 261 90 100
Columba livia Rock dove 296 XP_005499081.1 238 86 93
Pelodiscus sinensis Soft shell turtle 296 XP_006128883.1 216 94 72
Trichechus manatus latirostris Manatee 98.7 XP_004385839.1 242 78 100
Camelus ferus Camel 94.2 XP_006194022.1 261 99 100
Mus musculus Mouse 92.3 NP_780670.2 262 98 100
Microtus ochrogaster Prairie vole 92.3 XP_005370139.1 261 99 100
Loxodonta africana Elephant 98.7 XP_003415081.1 999 99 98
Macaca fascicularis Crab eating macaque 42.6 EHH50788.1 233 89 100
Pan paniscus Bonobo 42.6 XP_003824811.1 243 88 100

Structure

Gene

The FAM78B gene is located on the sense (negative) strand of chromosome 1 at location 1q24.1 and spans the chromosomal locus 166039271-166135909, covering a total of 96,638 base pairs along the chromosome, the FAM78B gene has 2 exons in its transcript mRNA of 1,481 bp.[2] FAM78B in humans is separated into two exons that have 95,243 bp of introns between them.[3] The gene is highly conserved in vertebrates (excluding arthropods) and the pacific clam and liver fluke.

mRNA

There is one isoform that has been identified in humans and is composed of two exons that composes a mRNA of 1481 bp.[4]

Protein

The FAM78B protein has a calculated molecular weight of 30 kDa, has a higher relative abundance of tryptophan (W), has a more greatly conserved c-terminal region, is composed of both alpha helix and beta strand, and resides in the nucleus of the cell after transcription [5]

General properties

The protein FAM78B consists of 254 amino acids with a predicted molecular weight of 30 kDal. The protein has an isoelectric point of 9.6. FAM78B has a highly conserved C terminus among its orthologs and is histidine poor.[6] The highest conserved amino acids are ISDSDG from aa 104-110, WLVA from aa 171-175, VDP---L--R from aa 199-208, and the C’ terminus, but especially NADQVLMW from aa 240-247.

Conservation

The amino acid sequence for FAM78B is highly conserved in mammals, having around 86% to 100% sequence similarity. Birds, frogs, mammals, and lizards also have a high degree of similarity to the human FAM78B sequence with similarities between 76% and 83%. Fish have between 56% and 66% sequence similarity. The C terminal end is the most highly conserved across ortholog-containing species from mammals to the pacific sea clam. [4]

Regulation

mRNA level

There is one miRNA binding site targeted by miR-24 for sequence CUGAGCCA in Homo sapiens located on the 3' end of the mRNA at 88-95 after the stop codon (bp 167,091,390-167,091,397 on chromosome 1). Stem loop from 155-172 of the 3' end of the mRNA matches with the miRNA site.[7]

Protein level

Conserved nuclear localization signal (RPKR) from aa 248-252.

Expression

FAM78B is generally ubiquitously expressed [8] and is highly expressed in regions of the brain.[9]

Clinical relevance

FAM78B is statistically significantly correlated to chronic kidney disease when there is one of three different single nucleotide polymorphisms (SNPs) including two located in the intron (rs2116519 and rs4074897) and one located in the 5’ UTR (rs987131).

References

  1. "SDSC Biology Workbench".
  2. "NCBI Gene". Retrieved 2014-04. Check date values in: |accessdate= (help)
  3. "USCS BLAT". Retrieved 2014-04. Check date values in: |accessdate= (help)
  4. "NCBI Nucleotide". Retrieved April 2014. Check date values in: |accessdate= (help)
  5. Nakai and Horton. "PSORTII". Retrieved April 2014. Check date values in: |accessdate= (help)
  6. "SAPS Biology Workbench". Retrieved 2014-04. Check date values in: |accessdate= (help)[permanent dead link]
  7. "mFold". Retrieved 2014-04. Check date values in: |accessdate= (help)
  8. "Gene Atlas".
  9. "NCBI Geo Profiles".

Further reading

  • Yamada Y, Nishida T, Ichihara S, Kato K, Fujimaki T, Oguri M, Horibe H, Yoshida T, Watanabe S, Satoh K, Aoyagi Y, Fukuda M, Sawabe M (June 2013). "Identification of chromosome 3q28 and ALPK1 as susceptibility loci for chronic kidney disease in Japanese individuals by a genome-wide association study". Journal of Medical Genetics. 50 (6): 410–8. doi:10.1136/jmedgenet-2013-101518. PMID 23539754.

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