FAM71E1 explained

FAM71E1, also known as Family With Sequence Similarity 71 Member E1, is a protein that in humans is encoded by the FAM71E1 gene. It is thought to be ubiquitously expressed at low levels throughout the body, and it is conserved in vertebrates, particularly mammals and some reptiles. The protein is localized to the nucleus and can be exported to the cytoplasm.

Gene

Location

The gene is located on the minus strand at 19q13.33 and spans from 50,466,643 to 50,476,753. It is 10,070 bp long.

Gene Neighborhood

In humans, the gene is flanked by the following genes:[1] [2]

Promoter

The promoter of FAM71E1 is located on the minus strand from 50,476,094 to 50,477,946 . It is 1,853 bp long.[7]

Expression

The gene seems to be ubiquitously expressed at low levels throughout the body [8] [9] [10] but has prominent expression in the adult human testis,[11] followed by lower expression levels in the sperm, oocyte, and brain.[12] [13] [14] [15] [16] Age does not have an effect on its expression in the skeletal muscle of males or females.[17] Its expression is elevated prior to the differentiation of embryonic stem cells into pancreatic islet-like cells.[18]

Transcript

Isoforms

The FAM71E1 gene produces two isoforms from alternative splicing. Isoform 1 is 1281 bp long, and isoform 2 is slightly shorter at 1233 bp long.[19] Both transcript variants have 5 exons, 4 of which are coding exons. The third intron for the isoform 2 transcript is longer than the one found in isoform 1.

Regulation

The FAM71E1 transcript is regulated by micro-RNAs, such as miR-149, miR-7, miR-125b, miR-125a-5p, miR192-5p, and miR-215.[20]

Protein

Properties

The protein from isoform 1 is 247 amino acids long with a molecular weight of 27.6 kDa. It has a charge of 5.0 and an isoelectric point of 8.9.[21] It has a domain of unknown function (DUF3699), which is conserved in eukaryotes and has no known pairwise interactions with other domains.[22] The structure of the protein has 3 alpha helices and 5 beta strands.

Localization

The protein is predicted to localize to the nucleus and thought to be mainly associated with the nucleoli fibrillar center.[23] It can also be exported to the cytoplasm.

Homologs

Paralogs

The FAM71E1 gene is fast evolving. It has the following 8 paralogs: FAM71A, FAM71B, FAM71C, FAM71D, FAM71E2, FAM71F1, FAM71F2, and AC020922.1. FAM71D, FAM71E2 and AC0209221.1 are found in Amniotes and their last common ancestor with FAM71E1 was likely in the ancestor of the Sauria taxon, which includes reptiles and birds. The remaining paralogs are found in mammals and are expressed in organisms from the evolutionary descendants of the lobe-finned fish (Sarcopterygii). Their last common ancestor with FAM71E1 was Coelacanth (Latimeria chalumnae).[24]

Paralog
Accession number Sequence length (aa) Sequence Identity (%) Sequence Similarity (%)
FAM71E1NM_001308429247100100
FAM71CNP_699195.124120.128.0
FAM71F1NP_115988.134416.324.2
FAM71F2NP_001012457.330915.423.8
FAM71DNP_775797.242212.016.5
AC020922.1Unavailable47211.116.3
FAM71ANP_705834.259410.814.5
FAM71BNP_570969.260510.213.9
FAM71E2NP_001138874.19226.89.0

Orthologs

Orthologs of FAM71E1 can be found only in vertebrates, primarily in placental mammals in the Boreoeutheria group and occasionally in a few reptilian species. Reptiles and marsupials are included in the distant homologs, while orthologs in placental animals such as rodents and primates are more closely related to FAM71E1. The gene history contains 27 duplication events and 1 splitting event.

Genus and species
Common Name Accession number Length (aa) Identity (%) Similarity (%)
Homo sapiensHumanNP_001295358247100100
Pan troglodytesChimpanzeeXP_009434364 2479897
Microcebus murinus Gray mouse lemur XP_012609669.1 2337982
Mus musculus House mouseNP_082445.1 2126872
Equus caballus HorseXP_023505998.1 1927679
Bos taurus CattleXP_010813399 2277579
Panthera pardus LeopardXP_019281103 2177176
Trichechus manatus latirostris Florida manatee XP_004381904 2197376
Phascolarctos cinereus KoalaXP_020827525 2316875
Python bivittatus Burmese pythonXP_007423163 1675064
Anolis carolinensisGreen anoleXP_0168501311313748

Clinical Significance

Mutations

There are no disease-causing mutations associated with this gene,[25] and it is tolerant towards loss-of-function variants.[26]

Disease Associations

FAM71E1 has reduced expression in Type 2 diabetes patients and is likely not involved in the disease's pathophysiology.[27] Its expression is also altered in Parkinson's disease[28] and several cancers, such as non-triple negative ductal carcinoma in situ,[29] breast cancer,[30] pancreatic adenocarcinoma, and colorectal carcinoma. It is a gene of interest in predicting susceptibility to pneumonia.[31]

Notes and References

  1. Web site: Human Gene FAM71E1 (ENST00000600100.5) Description and Page Index. genome.ucsc.edu. 2018-02-20.
  2. Web site: FAM71E1 family with sequence similarity 71 member E1 [Homo sapiens (human) ] ]. NCBI Gene .
  3. Web site: SPIB Gene. www.genecards.org. 2018-05-06.
  4. Web site: MYBPC2 Gene. www.genecards.org. 2018-05-06.
  5. Web site: EMC10 Gene. www.genecards.org. 2018-05-06.
  6. Web site: JOSD2 Gene. www.genecards.org. 2018-05-06.
  7. Web site: Genomatix - NGS Data Analysis & Personalized Medicine. www.genomatix.de. 2018-05-07. 2021-12-02. https://web.archive.org/web/20211202010908/https://www.genomatix.de/. dead.
  8. Web site: FAM71E1- Multiple normal tissues. www.ncbi.nlm.nih.gov. 2018-05-06.
  9. Web site: FAM71E1- Normal tissues of diverse types (SHBW). www.ncbi.nlm.nih.gov. 2018-05-06.
  10. Web site: AceView: Gene:FAM71E1, a comprehensive annotation of human, mouse and worm genes with mRNAs or ESTsAceView.. Danielle. Thierry-Mieg. Jean. Thierry-Mieg. www.ncbi.nlm.nih.gov. 2018-02-20.
  11. Kwon JT, Ham S, Jeon S, Kim Y, Oh S, Cho C . Expression of uncharacterized male germ cell-specific genes and discovery of novel sperm-tail proteins in mice . PLOS ONE . 12 . 7 . e0182038 . 2017-07-25 . 28742876 . 5526581 . 10.1371/journal.pone.0182038 . 2017PLoSO..1282038K . free .
  12. Web site: Gene: FAM71E1 - ENSG00000142530. bgee.org. en. 2018-05-06.
  13. Web site: Expression Atlas entry on FAM71E1. www.ebi.ac.uk. en. 2018-05-06.
  14. Web site: Genevisible entry on FAM71E1. Genevisible.
  15. Web site: Tissue expression of FAM71E1 - Summary - The Human Protein Atlas. www.proteinatlas.org. 2018-05-06.
  16. Web site: EST Profile - Hs.448941. www.ncbi.nlm.nih.gov. 2018-05-06.
  17. Web site: FAM71E1- Age effect on the skeletal muscle. www.ncbi.nlm.nih.gov. 2018-05-07.
  18. Web site: FAM71E1- Pancreatic islet-like cell clusters derived from T3 embryonic stem cells. www.ncbi.nlm.nih.gov. 2018-05-07.
  19. Web site: Homo sapiens family with sequence similarity 71 member E1 (FAM71E1), t - Nucleotide - NCBI. www.ncbi.nlm.nih.gov. 2018-02-20.
  20. Web site: miRNA entry on FAM71E1. 34.236.212.39. 2018-05-07. 2018-05-07. https://web.archive.org/web/20180507221416/http://34.236.212.39/microrna/getMrna.do?gene=112703&utr=316&organism=9606. dead.
  21. Web site: Transcript Summary on FAM71E1 . Vega .
  22. Web site: Results for pfam12480. bioinf.umbc.edu. 2018-05-07.
  23. Web site: CALIPHO Bioinformatics. www.nextprot.org. SIB Swiss Institute of Bioinformatics.
  24. Web site: Ensembl entry on FAM71E1 Gene Tree.
  25. Web site: Kann Laboratory- Domain Mapping of Disease Mutations entry on FAM71E1.
  26. Web site: ExAC entry on FAM71E1. exac.broadinstitute.org. 2018-05-06.
  27. Web site: FAM71E1- Type 2 diabetes and role of hepatokines. www.ncbi.nlm.nih.gov .
  28. Momcilovic O, Sivapatham R, Oron TR, Meyer M, Mooney S, Rao MS, Zeng X . Derivation, Characterization, and Neural Differentiation of Integration-Free Induced Pluripotent Stem Cell Lines from Parkinson's Disease Patients Carrying SNCA, LRRK2, PARK2, and GBA Mutations . PLOS ONE . 11 . 5 . e0154890 . May 2016 . 27191603 . 4871453 . 10.1371/journal.pone.0154890 . 2016PLoSO..1154890M . free .
  29. Brown. John . vanc . 2016. Immunohistochemical and genomic analysis of ductal carcinoma in situ of the human breast . Ph.D. . King's College London .
  30. Nisha. Kanwar . vanc . Ph.D. . March 2017 . Early Genomic Events Associated with Dissemination of Breast Cancer Cells . University of Toronto . 1807/77456 .
  31. Hayden LP, Cho MH, McDonald MN, Crapo JD, Beaty TH, Silverman EK, Hersh CP . Susceptibility to Childhood Pneumonia: A Genome-Wide Analysis . EN . American Journal of Respiratory Cell and Molecular Biology . 56 . 1 . 20–28 . January 2017 . 27508494 . 5248961 . 10.1165/rcmb.2016-0101oc .