HBE1

Hemoglobin subunit epsilon is a protein that in humans is encoded by the HBE1 gene.[5]

HBE1
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1A9W
Identifiers
Aliases	HBE1, HBE, hemoglobin subunit epsilon 1
External IDs	OMIM: 142100 MGI: 96024 HomoloGene: 110794 GeneCards: HBE1
Gene location (Human) Chr. Chromosome 11 (human)[1] Band 11p15.4 Start 5,268,345 bp[1] End 5,505,652 bp[1]
Gene location (Mouse) Chr. Chromosome 7 (mouse)[2] Band 7 E3|7 54.85 cM Start 103,841,637 bp[2] End 103,843,164 bp[2]
Gene ontology Molecular function • hemoglobin alpha binding • metal ion binding • heme binding • iron ion binding • oxygen binding • oxygen carrier activity • GO:0001948 protein binding • peroxidase activity • haptoglobin binding • organic acid binding Cellular component • cytosol • blood microparticle • hemoglobin complex • haptoglobin-hemoglobin complex Biological process • protein heterooligomerization • blood coagulation • oxygen transport • response to organic cyclic compound • transport • hydrogen peroxide catabolic process • cellular oxidant detoxification Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	3046	15132
Ensembl	ENSG00000213931	ENSMUSG00000052217
UniProt	P02100	P04444
RefSeq (mRNA)	NM_005330	NM_008219
RefSeq (protein)	NP_005321 NP_005321.1	NP_032245
Location (UCSC)	Chr 11: 5.27 – 5.51 Mb	Chr 7: 103.84 – 103.84 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

Function

The epsilon globin gene (HBE) is normally expressed in the embryonic yolk sac: two epsilon chains together with two zeta chains (an alpha-like globin) constitute the embryonic hemoglobin Hb Gower I; two epsilon chains together with two alpha chains form the embryonic Hb Gower II. Both of these embryonic hemoglobins are normally supplanted by fetal, and later, adult hemoglobin. The five beta-like globin genes are found within a 45 kb cluster on chromosome 11 in the following order: 5' - epsilon – gamma-G – gamma-A – delta – beta - 3'.[6]

See also

• Hemoglobin
• Human β-globin locus
• Hemoglobin alpha chains (two genes, same sequence):
  • HBA1
  • HBA2

References

1. GRCh38: Ensembl release 89: ENSG00000213931 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000052217 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. Higgs DR, Vickers MA, Wilkie AO, Pretorius IM, Jarman AP, Weatherall DJ (May 1989). "A review of the molecular genetics of the human alpha-globin gene cluster". Blood. 73 (5): 1081–104. doi:10.1182/blood.V73.5.1081.1081. PMID 2649166.
6. "Entrez Gene: HBE1 hemoglobin, epsilon 1".

Further reading

• Clegg JB (1982). "Embryonic hemoglobin: sequence of the epsilon and zeta chains". Tex. Rep. Biol. Med. 40: 23–8. PMID 6172865.
• Giardina B, Messana I, Scatena R, Castagnola M (1995). "The multiple functions of hemoglobin". Crit. Rev. Biochem. Mol. Biol. 30 (3): 165–96. doi:10.3109/10409239509085142. PMID 7555018.
• Chang JC, Kan YW (1979). "beta 0 thalassemia, a nonsense mutation in man". Proc. Natl. Acad. Sci. U.S.A. 76 (6): 2886–9. doi:10.1073/pnas.76.6.2886. PMC 383714. PMID 88735.
• Proudfoot NJ, Baralle FE (1980). "Molecular cloning of human epsilon-globin gene". Proc. Natl. Acad. Sci. U.S.A. 76 (11): 5435–9. doi:10.1073/pnas.76.11.5435. PMC 411663. PMID 160554.
• Proudfoot NJ, Brownlee GG (1976). "3' non-coding region sequences in eukaryotic messenger RNA". Nature. 263 (5574): 211–4. doi:10.1038/263211a0. PMID 822353.
• Marotta CA, Forget BG, Cohne-Solal M, et al. (1977). "Human beta-globin messenger RNA. I. Nucleotide sequences derived from complementary RNA". J. Biol. Chem. 252 (14): 5019–31. PMID 873928.
• Gelinas R, Endlich B, Pfeiffer C, et al. (1985). "G to A substitution in the distal CCAAT box of the A gamma-globin gene in Greek hereditary persistence of fetal haemoglobin". Nature. 313 (6000): 323–5. doi:10.1038/313323a0. PMID 2578619.
• Collins FS, Metherall JE, Yamakawa M, et al. (1985). "A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobin". Nature. 313 (6000): 325–6. doi:10.1038/313325a0. PMID 2578620.
• Lang KM, Spritz RA (1985). "Cloning specific complete polyadenylylated 3'-terminal cDNA segments". Gene. 33 (2): 191–6. doi:10.1016/0378-1119(85)90093-9. PMID 2581851.
• Ley TJ, Maloney KA, Gordon JI, Schwartz AL (1989). "Globin gene expression in erythroid human fetal liver cells". J. Clin. Invest. 83 (3): 1032–8. doi:10.1172/JCI113944. PMC 303780. PMID 2921315.
• Chabot B, Black DL, LeMaster DM, Steitz JA (1986). "The 3' splice site of pre-messenger RNA is recognized by a small nuclear ribonucleoprotein". Science. 230 (4732): 1344–9. doi:10.1126/science.2933810. PMID 2933810.
• Engelke DR, Hoener PA, Collins FS (1988). "Direct sequencing of enzymatically amplified human genomic DNA". Proc. Natl. Acad. Sci. U.S.A. 85 (2): 544–8. doi:10.1073/pnas.85.2.544. PMC 279587. PMID 3267215.
• Fei YJ, Stoming TA, Efremov GD, et al. (1988). "Beta-thalassemia due to a T----A mutation within the ATA box". Biochem. Biophys. Res. Commun. 153 (2): 741–7. doi:10.1016/S0006-291X(88)81157-4. PMID 3382401.
• Prchal JT, Cashman DP, Kan YW (1986). "Hemoglobin Long Island is caused by a single mutation (adenine to cytosine) resulting in a failure to cleave amino-terminal methionine". Proc. Natl. Acad. Sci. U.S.A. 83 (1): 24–7. doi:10.1073/pnas.83.1.24. PMC 322783. PMID 3455755.
• van Santen VL, Spritz RA (1985). "mRNA precursor splicing in vivo: sequence requirements determined by deletion analysis of an intervening sequence". Proc. Natl. Acad. Sci. U.S.A. 82 (9): 2885–9. doi:10.1073/pnas.82.9.2885. PMC 397671. PMID 3857622.
• Ruskin B, Greene JM, Green MR (1985). "Cryptic branch point activation allows accurate in vitro splicing of human beta-globin intron mutants". Cell. 41 (3): 833–44. doi:10.1016/S0092-8674(85)80064-7. PMID 3879973.
• Tuan D, Solomon W, Li Q, London IM (1985). "The "beta-like-globin" gene domain in human erythroid cells". Proc. Natl. Acad. Sci. U.S.A. 82 (19): 6384–8. doi:10.1073/pnas.82.19.6384. PMC 390720. PMID 3879975.
• Orkin SH, Antonarakis SE, Kazazian HH (1984). "Base substitution at position -88 in a beta-thalassemic globin gene. Further evidence for the role of distal promoter element ACACCC". J. Biol. Chem. 259 (14): 8679–81. PMID 6086605.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.