EPAS1 Gene

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1		Vivi Li	+ 416 word(s)	416	2020-12-15 07:51:48

This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/epas1

Endothelial PAS domain protein 1

genes

1. Normal Function

The EPAS1 gene, often known as HIF2A, provides instructions for making a protein called hypoxia-inducible factor 2-alpha (HIF-2α). This protein is one part (subunit) of a larger protein complex called HIF, which plays a critical role in the body's ability to adapt to changing oxygen levels. HIF controls several important genes involved in cell division, the formation of new blood vessels, and the production of red blood cells. It is the major regulator of a hormone called erythropoietin, which controls red blood cell production.

HIF-2α is constantly produced in the body. When adequate oxygen is available, other proteins target HIF-2α to be broken down (degraded) so it does not build up. However, when oxygen levels are lower than normal (hypoxia), HIF-2α is degraded at a slower rate. Consequently, more HIF is available to stimulate the formation of new blood vessels and the production of red blood cells. These activities help maximize the amount of oxygen that can be delivered to the body's organs and tissues.

Studies suggest that the EPAS1 gene is involved in the body's adaptation to high altitude. At higher altitudes, such as in mountainous regions, air pressure is lower and less oxygen enters the body through the lungs. Over time, the body compensates for the lower oxygen levels by changing breathing patterns and producing more red blood cells and blood vessels.

2. Health Conditions Related to Genetic Changes

2.1 Familial Erythrocytosis

At least five mutations in the EPAS1 gene have been found to cause familial erythrocytosis, an inherited condition characterized by an increased number of red blood cells and an elevated risk of abnormal blood clots. When familial erythrocytosis results from EPAS1 gene mutations, it is often designated ECYT4.

Mutations in the EPAS1 gene change single protein building blocks (amino acids) in the HIF-2α protein. These changes prevent HIF-2α from interacting normally with the proteins that target it for degradation. As a result, HIF-2α is not degraded efficiently, and HIF accumulates in cells even when adequate oxygen is available. The presence of extra HIF leads to the production of red blood cells when no more are needed, resulting in an excess of these cells in the bloodstream.

3. Other Names for This Gene

basic-helix-loop-helix-PAS protein MOP2
bHLHe73
class E basic helix-loop-helix protein 73
ECYT4
endothelial PAS domain-containing protein 1
EPAS-1
EPAS1_HUMAN
HIF-1-alpha-like factor
HIF-1alpha-like factor
HIF-2-alpha
HIF2-alpha
HIF2A
HLF
hypoxia-inducible factor 2 alpha
hypoxia-inducible factor 2-alpha
member of PAS protein 2
MOP2
PAS domain-containing protein 2
PASD2

References

Beall CM, Cavalleri GL, Deng L, Elston RC, Gao Y, Knight J, Li C, Li JC, LiangY, McCormack M, Montgomery HE, Pan H, Robbins PA, Shianna KV, Tam SC, Tsering N, Veeramah KR, Wang W, Wangdui P, Weale ME, Xu Y, Xu Z, Yang L, Zaman MJ, Zeng C,Zhang L, Zhang X, Zhaxi P, Zheng YT. Natural selection on EPAS1 (HIF2alpha)associated with low hemoglobin concentration in Tibetan highlanders. Proc NatlAcad Sci U S A. 2010 Jun 22;107(25):11459-64. doi: 10.1073/pnas.1002443107.
Furlow PW, Percy MJ, Sutherland S, Bierl C, McMullin MF, Master SR, Lappin TR,Lee FS. Erythrocytosis-associated HIF-2alpha mutations demonstrate a criticalrole for residues C-terminal to the hydroxylacceptor proline. J Biol Chem. 2009Apr 3;284(14):9050-8. doi: 10.1074/jbc.M808737200.
Lee FS, Percy MJ. The HIF pathway and erythrocytosis. Annu Rev Pathol.2011;6:165-92. doi: 10.1146/annurev-pathol-011110-130321. Review.
McMullin MF. HIF pathway mutations and erythrocytosis. Expert Rev Hematol.2010 Feb;3(1):93-101. doi: 10.1586/ehm.09.68. Review.
Percy MJ, Chung YJ, Harrison C, Mercieca J, Hoffbrand AV, Dinardo CL, SantosPC, Fonseca GH, Gualandro SF, Pereira AC, Lappin TR, McMullin MF, Lee FS. Two newmutations in the HIF2A gene associated with erythrocytosis. Am J Hematol. 2012Apr;87(4):439-42. doi: 10.1002/ajh.23123.
Percy MJ, Rumi E. Genetic origins and clinical phenotype of familial andacquired erythrocytosis and thrombocytosis. Am J Hematol. 2009 Jan;84(1):46-54.doi: 10.1002/ajh.21313. Review.
Percy MJ. Familial erythrocytosis arising from a gain-of-function mutation in the HIF2A gene of the oxygen sensing pathway. Ulster Med J. 2008 May;77(2):86-8. Review.
Perrotta S, Della Ragione F. The HIF2A gene in familial erythrocytosis. N EnglJ Med. 2008 May 1;358(18):1966; author reply 1966-7.
Simonson TS, McClain DA, Jorde LB, Prchal JT. Genetic determinants of Tibetan high-altitude adaptation. Hum Genet. 2012 Apr;131(4):527-33. doi:10.1007/s00439-011-1109-3.
van Wijk R, Sutherland S, Van Wesel AC, Huizinga EG, Percy MJ, Bierings M, LeeFS. Erythrocytosis associated with a novel missense mutation in the HIF2A gene.Haematologica. 2010 May;95(5):829-32. doi: 10.3324/haematol.2009.017582.

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Subjects: Genetics & Heredity

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Vivi Li

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Entry Collection: MedlinePlus

Update Date: 24 Dec 2020

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