View source for HEXA

{{Infobox_gene}}
[[File:HEXA location.png|thumb|HEXA gene is located on the long (q) arm of [[Chromosome 15 (human)|chromosome 15]] at position 24.1.]]
'''Hexosaminidase A (alpha polypeptide)''', also known as '''HEXA''', is an [[enzyme]] that in humans is encoded by the ''HEXA'' [[gene]], located on the [[Chromosome 15 (human)|15th chromosome]].<ref name="pmid3013851">{{cite journal | vauthors = Korneluk RG, Mahuran DJ, Neote K, Klavins MH, O'Dowd BF, Tropak M, Willard HF, Anderson MJ, Lowden JA, Gravel RA | title = Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease | journal = The Journal of Biological Chemistry | volume = 261 | issue = 18 | pages = 8407–13 | date = June 1986 | pmid = 3013851 | doi =  }}</ref><ref name="pmid2952641">{{cite journal | vauthors = Proia RL, Soravia E | title = Organization of the gene encoding the human beta-hexosaminidase alpha-chain | journal = The Journal of Biological Chemistry | volume = 262 | issue = 12 | pages = 5677–81 | date = April 1987 | pmid = 2952641 | doi =  }}</ref>

[[Hexosaminidase#Lysosomal isozymes A.2C B.2C and S|Hexosaminidase A]] and the cofactor [[GM2A|G<sub>M2</sub> activator protein]] catalyze the degradation of the G<sub>M2</sub> [[gangliosides]] and other molecules containing terminal N-acetyl hexosamines.<ref>{{cite journal |vauthors=Knapp S, Vocadlo D, Gao Z, Kirk B, Lou J, Withers SG | title = NAG-thiazoline, an N-acetylbeta-hexosaminidase inhibitor that implicates acetamido participation | journal = J. Am. Chem. Soc. | volume = 118 | issue = 28 | pages = 6804–6805 | year = 1996 | month = | pmid = | pmc = | doi = 10.1021/ja960826u }}</ref>   Hexosaminidase A is a [[heterodimer]] composed of an alpha subunit (this protein) and a [[HEXB|beta]] subunit.  The alpha subunit polypeptide is encoded by the ''HEXA'' gene while the beta subunit is encoded by the ''[[HEXB]]'' gene.  Gene mutations in the gene encoding the beta subunit (HEXB) often result in [[Sandhoff disease]]; whereas, [[mutations]] in the gene encoding the alpha subunit (HEXA, this gene) decrease the [[hydrolysis]] of G<sub>M2</sub> gangliosides, which is the main cause of [[Tay–Sachs disease]].<ref name="pmid12662933">{{cite journal | vauthors = Mark BL, Mahuran DJ, Cherney MM, Zhao D, Knapp S, James MN | title = Crystal structure of human beta-hexosaminidase B: understanding the molecular basis of Sandhoff and Tay-Sachs disease | journal = Journal of Molecular Biology | volume = 327 | issue = 5 | pages = 1093–109 | date = April 2003 | pmid = 12662933 | pmc = 2910754 | doi = 10.1016/S0022-2836(03)00216-X }}</ref>

== Function ==

Even though the alpha and beta subunits of hexosaminidase A can both cleave GalNAc residues, only the alpha subunit is able to [[hydrolyze]] G<sub>M2</sub> gangliosides. The alpha subunit contains a key residue, [[Arginine|Arg]]-424, which is essential for binding the N-acetyl-neuramanic residue of G<sub>M2</sub> gangliosides.   The alpha subunit can hydrolyze G<sub>M2</sub> gangliosides because it contains a loop structure consisting of the amino acids: [[Glycine|Gly]]-280, [[Serine|Ser]]-281, [[Glutamic acid|Glu]]-282, and [[Proline|Pro]]-283.  The loop is absent in the beta subunit, but it serves as an ideal structure for the binding of the G<sub>M2</sub> activator protein (G<sub>M2</sub>AP) in the alpha subunit.  A combination of Arg-424 and the amino acids that cause the formation of the loop allow the alpha subunit to hydrolyze G<sub>M2</sub> gangliosides into G<sub>M3</sub> gangliosides by removing the N-acetylgalactosamine (GalNAc) residue from G<sub>M2</sub> gangliosides.<ref name="Lemieux">{{cite journal | vauthors = Lemieux MJ, Mark BL, Cherney MM, Withers SG, Mahuran DJ, James MN | title = Crystallographic structure of human beta-hexosaminidase A: interpretation of Tay-Sachs mutations and loss of GM2 ganglioside hydrolysis | journal = Journal of Molecular Biology | volume = 359 | issue = 4 | pages = 913–29 | date = June 2006 | pmid = 16698036 | pmc = 2910082 | doi = 10.1016/j.jmb.2006.04.004 }}</ref>

== Gene mutations resulting in Tay&ndash;Sachs disease ==

There are numerous mutations that lead to hexosaminidase A deficiency including gene deletions, nonsense mutations, and missense mutations.  Tay&ndash;Sachs disease occurs when hexosaminidase A loses its ability to function. People with Tay&ndash;Sachs disease are unable to remove the GalNAc residue from the G<sub>M2</sub> ganglioside, and as a result, they end up storing 100 to 1000 times more  G<sub>M2</sub> gangliosides in the brain than the normal person.  Over 100 different mutations have been discovered just in infantile cases of Tay&ndash;Sachs disease alone.<ref name="Nyhan">{{cite book |vauthors=Ozand PT, Nyhan WL, Barshop BA | title = Atlas of metabolic diseases | edition = | publisher = Hodder Arnold | location = London | year = 2005 | origyear = | pages = 539–546 | quote = | isbn = 0-340-80970-1 | chapter = Part Thirteen Lipid Storage Disorders: Tay-Sachs disease/hexosaminidase A deficiency }}</ref>

The most common mutation, which occurs in over 80 percent of Tay&ndash;Sachs patients, results from a four base pair addition (TATC) in exon 11 of the Hex A gene. This insertion leads to an early stop [[codon]], which causes the Hex A deficiency.<ref>{{cite journal | vauthors = Boles DJ, Proia RL | title = The molecular basis of HEXA mRNA deficiency caused by the most common Tay-Sachs disease mutation | journal = American Journal of Human Genetics | volume = 56 | issue = 3 | pages = 716–24 | date = March 1995 | pmid = 7887427 | pmc = 1801160 | doi =  }}</ref>

Children born with Tay&ndash;Sachs usually die between two and six years of age from aspiration and [[pneumonia]]. Tay&ndash;Sachs causes cerebral degeneration and blindness. Patients also experience flaccid extremities and seizures. There is no cure for Tay&ndash;Sachs disease.<ref name=Nyhan/>

== Gene Therapies for Tay-Sachs ==
The HEXA gene is a protein encoding gene that codes for the lysosomal enzyme beta-hexosaminidase. This enzyme, combined with the GM2 activator protein, is responsible for the breakdown of ganglioside GM2 within the lysosome. Defects in the HEXA gene, however, prevent this degradation, leading to a buildup of toxins in brain and spinal cord cells. This fatal genetic disorder is called Tay-Sachs disease. Because the Tay-Sachs gene defect mainly affects neural cells, a patient with the HEXA mutation will experience a quick deterioration of motor and mental function before dying around the age of three or four. [8]

A “knockout” model, which is a mouse that has been genetically modified to observe the effects of inactivation of or damage to certain genes, found that the mice that were administered the HEXA gene experienced many of the same symptoms of Tay-Sachs, with one exception: GM2 buildup was distributed differently in the brains of the mice than in those of a typical human Tay-Sachs patient. [9] This model has allowed scientists to research gene therapies for HEXA defects. One study, done on mice, successfully reestablished beta-hexoaminidase levels and removed the toxic cell buildup by using a non-replicated Herpes simplex vector to code for the missing gene. [10]

== References ==
{{Reflist|33em}}

== Further reading ==
{{refbegin|33em}}
* {{cite journal | last1 = Taniike | first1 = Masako | last2 = Yamanaka | first2 = Shoji | last3 = Proia | first3 = Richard L. | last4 = Langaman | first4 = Clarita | last5 = Bone-Turrentine | first5 = Teresa | last6 = Suzuki | first6 = Kinuko | year = 1995 | title = Neuropathology of mice with targeted disruption of Hexa gene, a model of Tay-Sachs disease | url = | journal = Acta Neuropathologica | volume = 89 | issue = 4| pages = 296–304 | doi=10.1007/s004010050250| pmid = 7610760 }}
* {{cite journal | vauthors = Martino S, Marconi P, Tancini B, Dolcetta D, De Angelis MG, Montanucci P, Bregola G, Sandhoff K, Bordignon C, Emiliani C, Manservigi R, Orlacchio A | title = A direct gene transfer strategy via brain internal capsule reverses the biochemical defect in Tay-Sachs disease | journal = Human Molecular Genetics | volume = 14 | issue = 15 | pages = 2113–23 | date = August 2005 | pmid = 15961412 | doi = 10.1093/hmg/ddi216 }}
* {{cite journal | vauthors = Mahuran DJ | title = The biochemistry of HEXA and HEXB gene mutations causing GM2 gangliosidosis | journal = Biochimica et Biophysica Acta | volume = 1096 | issue = 2 | pages = 87–94 | date = February 1991 | pmid = 1825792 | doi = 10.1016/0925-4439(91)90044-A }}
* {{cite journal | vauthors = Myerowitz R | title = Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene | journal = Human Mutation | volume = 9 | issue = 3 | pages = 195–208 | year = 1997 | pmid = 9090523 | doi = 10.1002/(SICI)1098-1004(1997)9:3<195::AID-HUMU1>3.0.CO;2-7 }}
* {{cite journal | vauthors = Mahuran DJ | title = Biochemical consequences of mutations causing the GM2 gangliosidoses | journal = Biochimica et Biophysica Acta | volume = 1455 | issue = 2–3 | pages = 105–38 | date = October 1999 | pmid = 10571007 | doi = 10.1016/S0925-4439(99)00074-5 }}
* {{cite journal | vauthors = Gilbert F, Kucherlapati R, Creagan RP, Murnane MJ, Darlington GJ, Ruddle FH | title = Tay-Sachs' and Sandhoff's diseases: the assignment of genes for hexosaminidase A and B to individual human chromosomes | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 72 | issue = 1 | pages = 263–7 | date = January 1975 | pmid = 1054503 | pmc = 432284 | doi = 10.1073/pnas.72.1.263 }}
* {{cite journal | vauthors = Trop I, Kaplan F, Brown C, Mahuran D, Hechtman P | title = A glycine250--> aspartate substitution in the alpha-subunit of hexosaminidase A causes juvenile-onset Tay-Sachs disease in a Lebanese-Canadian family | journal = Human Mutation | volume = 1 | issue = 1 | pages = 35–9 | year = 1993 | pmid = 1301189 | doi = 10.1002/humu.1380010106 }}
* {{cite journal | vauthors = Akalin N, Shi HP, Vavougios G, Hechtman P, Lo W, Scriver CR, Mahuran D, Kaplan F | title = Novel Tay-Sachs disease mutations from China | journal = Human Mutation | volume = 1 | issue = 1 | pages = 40–6 | year = 1993 | pmid = 1301190 | doi = 10.1002/humu.1380010107 }}
* {{cite journal | vauthors = Akerman BR, Zielenski J, Triggs-Raine BL, Prence EM, Natowicz MR, Lim-Steele JS, Kaback MM, Mules EH, Thomas GH, Clarke JT | title = A mutation common in non-Jewish Tay-Sachs disease: frequency and RNA studies | journal = Human Mutation | volume = 1 | issue = 4 | pages = 303–9 | year = 1993 | pmid = 1301938 | doi = 10.1002/humu.1380010407 }}
* {{cite journal | vauthors = Fernandes M, Kaplan F, Natowicz M, Prence E, Kolodny E, Kaback M, Hechtman P | title = A new Tay-Sachs disease B1 allele in exon 7 in two compound heterozygotes each with a second novel mutation | journal = Human Molecular Genetics | volume = 1 | issue = 9 | pages = 759–61 | date = December 1992 | pmid = 1302612 | doi = 10.1093/hmg/1.9.759 }}
* {{cite journal | vauthors = McDowell GA, Mules EH, Fabacher P, Shapira E, Blitzer MG | title = The presence of two different infantile Tay-Sachs disease mutations in a Cajun population | journal = American Journal of Human Genetics | volume = 51 | issue = 5 | pages = 1071–7 | date = November 1992 | pmid = 1307230 | pmc = 1682822 | doi =  }}
* {{cite journal | vauthors = Whitley CB, Anderson RA, McIvor RS | title = Heterozygosity for the "DN allele" (G533-greater than A) of the beta-hexosaminidase alpha subunit gene identified by direct DNA sequencing in a family with the B1 variant of GM2-gangliosidosis | journal = Neuropediatrics | volume = 23 | issue = 2 | pages = 96–101 | date = April 1992 | pmid = 1318511 | doi = 10.1055/s-2008-1071320 }}
* {{cite journal | vauthors = Triggs-Raine BL, Mules EH, Kaback MM, Lim-Steele JS, Dowling CE, Akerman BR, Natowicz MR, Grebner EE, Navon R, Welch JP | title = A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening | journal = American Journal of Human Genetics | volume = 51 | issue = 4 | pages = 793–801 | date = October 1992 | pmid = 1384323 | pmc = 1682803 | doi =  }}
* {{cite journal | vauthors = Hechtman P, Boulay B, De Braekeleer M, Andermann E, Melançon S, Larochelle J, Prevost C, Kaplan F | title = The intron 7 donor splice site transition: a second Tay-Sachs disease mutation in French Canada | journal = Human Genetics | volume = 90 | issue = 4 | pages = 402–6 | date = December 1992 | pmid = 1483696 | doi = 10.1007/bf00220467 }}
* {{cite journal | vauthors = Mules EH, Hayflick S, Miller CS, Reynolds LW, Thomas GH | title = Six novel deleterious and three neutral mutations in the gene encoding the alpha-subunit of hexosaminidase A in non-Jewish individuals | journal = American Journal of Human Genetics | volume = 50 | issue = 4 | pages = 834–41 | date = April 1992 | pmid = 1532289 | pmc = 1682641 | doi =  }}
* {{cite journal | vauthors = Weitz G, Proia RL | title = Analysis of the glycosylation and phosphorylation of the alpha-subunit of the lysosomal enzyme, beta-hexosaminidase A, by site-directed mutagenesis | journal = The Journal of Biological Chemistry | volume = 267 | issue = 14 | pages = 10039–44 | date = May 1992 | pmid = 1533633 | doi =  }}
* {{cite journal | vauthors = Navon R, Proia RL | title = Tay-Sachs disease in Moroccan Jews: deletion of a phenylalanine in the alpha-subunit of beta-hexosaminidase | journal = American Journal of Human Genetics | volume = 48 | issue = 2 | pages = 412–9 | date = February 1991 | pmid = 1825014 | pmc = 1683003 | doi =  }}
* {{cite journal | vauthors = Mules EH, Dowling CE, Petersen MB, Kazazian HH, Thomas GH | title = A novel mutation in the invariant AG of the acceptor splice site of intron 4 of the beta-hexosaminidase alpha-subunit gene in two unrelated American black GM2-gangliosidosis (Tay-Sachs disease) patients | journal = American Journal of Human Genetics | volume = 48 | issue = 6 | pages = 1181–5 | date = June 1991 | pmid = 1827945 | pmc = 1683116 | doi =  }}
* {{cite journal | vauthors = Nakai H, Byers MG, Nowak NJ, Shows TB | title = Assignment of beta-hexosaminidase A alpha-subunit to human chromosomal region 15q23----q24 | journal = Cytogenetics and Cell Genetics | volume = 56 | issue = 3–4 | pages = 164 | year = 1991 | pmid = 1829032 | doi = 10.1159/000133077 }}
* {{cite journal | vauthors = Nishimoto J, Tanaka A, Nanba E, Suzuki K | title = Expression of the beta-hexosaminidase alpha subunit gene with the four-base insertion of infantile Jewish Tay-Sachs disease | journal = The Journal of Biological Chemistry | volume = 266 | issue = 22 | pages = 14306–9 | date = August 1991 | pmid = 1830584 | doi =  }}
* {{cite journal | vauthors = dos Santos MR, Tanaka A, sá Miranda MC, Ribeiro MG, Maia M, Suzuki K | title = GM2-gangliosidosis B1 variant: analysis of beta-hexosaminidase alpha gene mutations in 11 patients from a defined region in Portugal | journal = American Journal of Human Genetics | volume = 49 | issue = 4 | pages = 886–90 | date = October 1991 | pmid = 1832817 | pmc = 1683169 | doi =  }}
{{refend}}

== External links ==
{{Commons category|HEXA}}
* {{MeshName|Hexosaminidase A}}
* {{EC number|3.2.1.52}}
* [https://web.archive.org/web/20091201100319/http://www.tay-sachs.org/taysachs.php National Tay-Sach’s Disease Site]

{{PDB Gallery|geneid=3073}}
{{Sugar hydrolases}}
{{Glycolipid/sphingolipid metabolism enzymes}}

[[Category:Genes on human chromosome 15]]