Wikipedia

GATA3

GATA3 is a transcription factor that in humans is encoded by the GATA3 gene. Studies in animal models and humans indicate that it controls the expression of a wide range of biologically and clinically important genes.[5][6][7]

GATA3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesGATA3, HDR, HDRS, GATA binding protein 3
External IDsOMIM: 131320; MGI: 95663; HomoloGene: 1550; GeneCards: GATA3; OMA:GATA3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

2625

14462

Ensembl

ENSG00000107485

ENSMUSG00000015619

UniProt

P23771

P23772

RefSeq (mRNA)

NM_001002295
NM_002051

NM_008091
NM_001355110
NM_001355111
NM_001355112

RefSeq (protein)

NP_001002295
NP_002042

NP_032117
NP_001342039
NP_001342040
NP_001342041

Location (UCSC)Chr 10: 8.05 – 8.08 MbChr 2: 9.86 – 9.89 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

The GATA3 transcription factor is critical for the embryonic development of various tissues as well as for inflammatory and humoral immune responses and the proper functioning of the endothelium of blood vessels. GATA3 plays central role in allergy and immunity against worm infections.[8][9] GATA3 haploinsufficiency (i.e. loss of one or the two inherited GATA3 genes) results in a congenital disorder termed the Barakat syndrome.[10][11][12]

Current clinical and laboratory research is focusing on determining the benefits of directly or indirectly blocking the action of GATA3 in inflammatory and allergic diseases such as asthma.[10] It is also proposed to be a clinically important marker for various types of cancer, particularly those of the breast. However, the role, if any, of GATA3 in the development of these cancers is under study and remains unclear.[13]

Gene

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The GATA3 gene is located close to the end of the short arm of chromosome 10 at position p14. It consists of 8 exons, and codes for two variants viz., GATA3, variant 1, and GATA3, variant 2.[14] Expression of GATA3 may be regulated in part or at times by the antisense RNA, GATA3-AS1, whose gene is located close to the GATA3 gene on the short arm of chromosome 10 at position p14.[15] Various types of mutations including point mutations as well as small- and large-scale deletional mutations cause an autosomal dominant genetic disorder, the Barakat syndrome (also termed hypoparathyroidism, deafness, and renal dysplasia syndrome). The location of GATA3 borders that of other critical sites on chromosome 10, particularly a site located at 10p14-p13. Mutations in this site cause the congenital disorder DiGeorge syndrome/velocardiofacial syndrome complex 2 (or DiGeorge syndrome 2).[16] Large-scale deletions in GATA3 may span into the DiGeorge syndrome 2 area and thereby cause a complex syndrome with features of the Barakat syndrome combined with some of those of the DiGeorge syndrome 2.[12][17] Knockout of both GATA3 genes in mice is fatal: these animals die at embryonic days 11 and 12 due to internal bleeding. They also exhibit gross deformities in the brain and spine as well as aberrations in fetal liver hematopoiesis.[18]

Protein

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GATA3 variant 1 is a linear protein consisting of 444 amino acids. GATA3 variant 2 protein is an identically structured isoform of, but 1 amino acid shorter than, GATA3 variant 1. Differences, if any, in the functions of these two variants have not been reported.[19] With respect to the best studied variant, variant 1, but presumably also variant 2, one of the zinc finger structural motifs, ZNF2, is located at the protein's C-terminus and binds to specific gene promoter DNA sequences to regulate the expression of the genes controlled by these promoters. The other zinc finger, ZNF1, is at the protein's N-terminus and interacts with various nuclear factors, including Zinc finger protein 1 (i.e. ZFPM1, also termed Friends of GATA1 [i.e. FOG-1]) and ZFPM2 (i.e. FOG-2), that modulate GATA3's gene-stimulating actions.[20]

Pathophysiology

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The GATA3 transcription factor regulates the expression of genes involved in the development of various tissues as well as genes involved in physiological as well as pathological humoral inflammatory and allergic responses.[12][10]

Function

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GATA3 belongs to the GATA family of transcription factors. Gene-deletion studies in mice indicate that Gata3 (mouse gene equivalent to GATA3) is critical for the embryonic development and/or function of various cell types (e.g. fat cells, neural crest cells, lymphocytes) and tissues (e.g. kidney, liver, brain, spinal cord, mammary gland).[11] Studies in humans implicate GATA3 in the following:

  • 1) GATA3 is required for the development of the parathyroid gland, sensory components of the auditory system, and the kidney in animals and humans.[12] It may also contribute to the development of the vagina and uterus in humans.[11]
  • 2) In humans, GATA3 is required for the development and/or function of innate lymphoid cells (ILCs), particularly Group 2 ILCs as well as for the development of T helper cells,(Th cells), particularly Th2 cells. Group 2 ILCs and Th2 cells, and thereby GATA3, are critical for the development of allergic and humoral immune responses in humans. Comparable studies in animals implicate GATA3 in the development of lymphocytes that mediate allergic and humoral immunity as well as allergic and humoral immune responses.[21][11]
  • 3) GATA3 promotes the secretion of IL-4, IL-5, and IL-13 from Th2 cells in humans and has similar actions on comparable mouse lymphocytes. All three of these interleukins serve to promote allergic responses,[22]
  • 4) GATA3 induces the maturation of precursor cells into breast epithelial cells and maintains these cells in their mature state in mice and possibly humans.[23][24]
  • 5) In mice, GATA3 is responsible for the normal development of various tissues including the skin, fat cells, the thymus, and the nervous system.[25][11]

Clinical significance

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Mutations

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Inactivating mutations in one of the two parental GATA3 genes cause the congenital disorder of hypoparathyroidism with sensorineural deafness and kidney malformations, i.e. the Barakat syndrome. This rare syndrome may occur in families or as a new mutation in an individual from a family with no history of the disorder. Mutations in GATA3 cause variable degrees of hypoparathyroidism, deafness, and kidney disease birth defects because of 1) individual differences in the penetrance of the mutation, 2) a sporadic, and as yet unexplained, association with malformation of uterus and vagina, and 3) mutations which extend beyond the GATA3 gene into chromosomal areas where mutations are responsible for developing other types of abnormalities which are characteristics of the DeGeorge syndrome 2. The Barakat syndrome is due to a haploinsufficiency in GATA3 levels, i.e. levels of the transcription factor that are insufficient for the normal development of the cited tissues during embryogenesis.[11][12][17]

Allergy

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Mouse studies indicate that inhibiting the expression of GATA3 using antisense RNA methods suppresses allergic inflammation. The protein is overexpressed in the afflicted tissues of individuals with various forms of allergy including asthma, rhinitis, nasal polyps, and atopic eczema. This suggests that it may have a role in promoting these disorders.[26] In a phase IIA clinical study of individuals suffering allergen-induced asthma, inhalation of Deoxyribozyme ST010, which specifically inactivates GATA3 messenger RNA, for 28 days reduced early and late immune lung responses to inhaled allergen. The clinical benefit of inhibiting GATA3 in this disorder is thought to be due to interfering with the function of Group 2 ILCs and Th2 cells by, for example, reducing their production of IL-4, IL-13, and especially IL-5. Reduction in these eosinophil-stimulating interleukins, it is postulated, reduces this cells ability to promote allergic reactivity and responses.[10][27] For similar reasons, this treatment might also prove to be clinical useful for treating other allergic disorders.[26]

Tumors

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Breast tumors

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Development
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GATA3 is one of the three genes mutated in >10% of breast cancers (Cancer Genome Atlas).[28] Studies in mice indicate that the gene is critical for the normal development of breast tissue and directly regulates luminal cell (i.e. cells lining mammary ducts) differentiation in experimentally induced breast cancer.[18][29] Analytic studies of human breast cancer tissues suggest that GATA3 is required for specific type of low risk breast cancer (i.e. luminal A), is integral to the expression of estrogen receptor alpha, and (in estrogen receptor negative/androgen receptor positive cancers) androgen receptor signaling.[30][31][32] These studies suggest that GATA3 is involved in the development of at least certain types of breast cancer in humans. However, there is disagreement on this, with some studies suggesting that the expression of the GATA3 acts to inhibit and other studies suggesting that it acts to promote the development, growth, and/or spread of this cancer. Further studies are needed to elucidate the role, if any, of GATA3 in the development of breast cancer.[18]

Marker
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Immuocytochemical analysis of GATA3 protein in breast cells is a valuable marker for diagnosing primary breast cancer, being tested as positive in up to 94% of cases. It is especially valuable for estrogen receptor positive breast cancers but is less sensitive (435-66% elevated), although still more valuable than many other markers, for diagnosing triple-negative breast cancers. This analysis is widely used as a clinically valuable marker for breast cancer.[33][34]

Other tumor types

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Similar to breast tumors, the role of GATA3 in the genesis of other tumor types is unclear but detection of its transcription factor product may be diagnostically useful. Immuocytochemical analysis of GATA3 protein is considered a valuable marker for certain types of urinary bladder and urethral cancers as well as for parathyroid gland tumors (cancerous or benign), Single series reports suggest that this analysis might also be of value for diagnosing salivary gland tumors, salivary duct carcinomas, mammary analog secretory carcinomas, benign ovarian Brenner tumors, benign Walthard cell rests, and paragangliomas.[35][13]

Interactions

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GATA3 has been shown to interact with the following transcription factor regulators: ZFPM1 and ZFPM2;[20] LMO1;[36][37] and FOXA1.[38] These regulators may promote or inhibit GATA3 in stimulating the expression of its _target genes.

See also

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References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000107485 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000015619 – 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. ^ Joulin V, Bories D, Eléouet JF, Labastie MC, Chrétien S, Mattéi MG, et al. (Jul 1991). "A T-cell specific TCR delta DNA binding protein is a member of the human GATA family". The EMBO Journal. 10 (7): 1809–16. doi:10.1002/j.1460-2075.1991.tb07706.x. PMC 452855. PMID 2050118.
  6. ^ Yamashita M, Ukai-Tadenuma M, Miyamoto T, Sugaya K, Hosokawa H, Hasegawa A, et al. (Jun 2004). "Essential role of GATA3 for the maintenance of type 2 helper T (Th2) cytokine production and chromatin remodeling at the Th2 cytokine gene loci". The Journal of Biological Chemistry. 279 (26): 26983–90. doi:10.1074/jbc.M403688200. PMID 15087456.
  7. ^ "GATA3 GATA binding protein 3". Entrez Gene. National Center for Biotechnology Information (NCBI), U.S. National Institutes of Health.
  8. ^ Zheng W, Flavell RA (May 1997). "The Transcription Factor GATA-3 Is Necessary and Sufficient for Th2 Cytokine Gene Expression in CD4 T Cells". Cell. 89 (4): 587–596. doi:10.1016/s0092-8674(00)80240-8. PMID 9160750. S2CID 18342599.
  9. ^ Zheng WP, Flavell RA (June 2016). "Pillars Article: The Transcription Factor GATA-3 Is Necessary and Sufficient for Th2 Cytokine Gene Expression in CD4 T Cells. Cell. 1997. 89: 587-596". Journal of Immunology. 196 (11): 4426–4435. PMID 27207805.
  10. ^ a b c d Barnes PJ (July 2018). "_targeting cytokines to treat asthma and chronic obstructive pulmonary disease". Nature Reviews. Immunology. 18 (7): 454–466. doi:10.1038/s41577-018-0006-6. PMID 29626211. S2CID 4647119.
  11. ^ a b c d e f "GATA-Binding Protein; GATA3". Online Mendelian Inheritance in Man (OMIM). Entry 131320.
  12. ^ a b c d e Belge H, Dahan K, Cambier JF, Benoit V, Morelle J, Bloch J, et al. (May 2017). "Clinical and mutational spectrum of hypoparathyroidism, deafness and renal dysplasia syndrome". Nephrology, Dialysis, Transplantation. 32 (5): 830–837. doi:10.1093/ndt/gfw271. PMID 27387476.
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  14. ^ "Homo sapiens GATA binding protein 3 (GATA3)". RefSeqGene on Chromosome - Nucleotide. National Center for Biotechnology Information (NCBI), U.S. National Institutes of Health. 2019-05-21.
  15. ^ "GATA3-AS1 GATA3 antisense RNA 1 [Homo sapiens (human)". Entrez Gene. National Center for Biotechnology Information (NCBI), U.S. National Institutes of Health.
  16. ^ "DiGeorge syndrome/velocardiofacial syndrome complex 2 - Conditions". Genetics Testing Registry (GTR). National Center for Biotechnology Information (NCBI), U.S. National Institutes of Health.
  17. ^ a b Lindstrand A, Malmgren H, Verri A, Benetti E, Eriksson M, Nordgren A, et al. (May 2010). "Molecular and clinical characterization of patients with overlapping 10p deletions". American Journal of Medical Genetics. Part A. 152A (5): 1233–43. doi:10.1002/ajmg.a.33366. PMID 20425828. S2CID 22213304.
  18. ^ a b c Du F, Yuan P, Wang T, Zhao J, Zhao Z, Luo Y, et al. (November 2015). "The Significance and Therapeutic Potential of GATA3 Expression and Mutation in Breast Cancer: A Systematic Review". Medicinal Research Reviews. 35 (6): 1300–15. doi:10.1002/med.21362. PMID 26313026. S2CID 11668034.
  19. ^ "Homo sapiens GATA binding protein 3 (GATA3), transcript variant 2, mRN - Nucleotide". National Center for Biotechnology Information (NCBI), U.S. National Institutes of Health. 2019-05-19.
  20. ^ a b "trans-acting T-cell-specific transcription factor GATA-3 isoform 1 [Ho - Protein - NCBI". National Center for Biotechnology Information (NCBI), U.S. National Institutes of Health.
  21. ^ Zhu J (2017). "GATA3 Regulates the Development and Functions of Innate Lymphoid Cell Subsets at Multiple Stages". Frontiers in Immunology. 8: 1571. doi:10.3389/fimmu.2017.01571. PMC 5694433. PMID 29184556.
  22. ^ Yagi R, Zhu J, Paul WE (Jul 2011). "An updated view on transcription factor GATA3-mediated regulation of Th1 and Th2 cell differentiation Z". International Immunology. 23 (7): 415–20. doi:10.1093/intimm/dxr029. PMC 3123974. PMID 21632975.
  23. ^ Kouros-Mehr H, Slorach EM, Sternlicht MD, Werb Z (Dec 2006). "GATA-3 maintains the differentiation of the luminal cell fate in the mammary gland". Cell. 127 (5): 1041–55. doi:10.1016/j.cell.2006.09.048. PMC 2646406. PMID 17129787.
  24. ^ Asch-Kendrick R, Cimino-Mathews A (February 2016). "The role of GATA3 in breast carcinomas: a review". Human Pathology. 48: 37–47. doi:10.1016/j.humpath.2015.09.035. PMID 26772397.
  25. ^ Ho IC, Pai SY (February 2007). "GATA-3 - not just for Th2 cells anymore". Cellular & Molecular Immunology. 4 (1): 15–29. PMID 17349208.
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  27. ^ Garn H, Renz H (January 2017). "GATA-3-specific DNAzyme - A novel approach for stratified asthma therapy". European Journal of Immunology. 47 (1): 22–30. doi:10.1002/eji.201646450. PMID 27910098.
  28. ^ Koboldt DC, Fulton RS, McLellan MD (Oct 2012). "Comprehensive molecular portraits of human breast tumours". Nature. 490 (7418): 61–70. Bibcode:2012Natur.490...61T. doi:10.1038/nature11412. PMC 3465532. PMID 23000897.
  29. ^ Kouros-Mehr H, Bechis SK, Slorach EM, Littlepage LE, Egeblad M, Ewald AJ, et al. (Feb 2008). "GATA-3 links tumor differentiation and dissemination in a luminal breast cancer model". Cancer Cell. 13 (2): 141–52. doi:10.1016/j.ccr.2008.01.011. PMC 2262951. PMID 18242514.
  30. ^ Wilson BJ, Giguère V (2008). "Meta-analysis of human cancer microarrays reveals GATA3 is integral to the estrogen receptor alpha pathway". Molecular Cancer. 7: 49. doi:10.1186/1476-4598-7-49. PMC 2430971. PMID 18533032.
  31. ^ Dydensborg AB, Rose AA, Wilson BJ, Grote D, Paquet M, Giguère V, et al. (Jul 2009). "GATA3 inhibits breast cancer growth and pulmonary breast cancer metastasis". Oncogene. 28 (29): 2634–42. doi:10.1038/onc.2009.126. PMID 19483726. S2CID 2923763.
  32. ^ Sanga S, Broom BM, Cristini V, Edgerton ME (2009). "Gene expression meta-analysis supports existence of molecular apocrine breast cancer with a role for androgen receptor and implies interactions with ErbB family". BMC Medical Genomics. 2: 59. doi:10.1186/1755-8794-2-59. PMC 2753593. PMID 19747394.
  33. ^ Liu H, Shi J, Wilkerson ML, Lin F (July 2012). "Immunohistochemical evaluation of GATA3 expression in tumors and normal tissues: a useful immunomarker for breast and urothelial carcinomas". American Journal of Clinical Pathology. 138 (1): 57–64. doi:10.1309/AJCP5UAFMSA9ZQBZ. PMID 22706858.
  34. ^ Peng Y, Butt YM, Chen B, Zhang X, Tang P (August 2017). "Update on Immunohistochemical Analysis in Breast Lesions". Archives of Pathology & Laboratory Medicine. 141 (8): 1033–1051. doi:10.5858/arpa.2016-0482-RA. PMID 28574279.
  35. ^ Inamura K (April 2018). "Bladder Cancer: New Insights into Its Molecular Pathology". Cancers. 10 (4): 100. doi:10.3390/cancers10040100. PMC 5923355. PMID 29614760.
  36. ^ Ono Y, Fukuhara N, Yoshie O (Dec 1998). "TAL1 and LIM-only proteins synergistically induce retinaldehyde dehydrogenase 2 expression in T-cell acute lymphoblastic leukemia by acting as cofactors for GATA3". Molecular and Cellular Biology. 18 (12): 6939–50. doi:10.1128/MCB.18.12.6939. PMC 109277. PMID 9819382.
  37. ^ Ono Y, Fukuhara N, Yoshie O (Feb 1997). "Transcriptional activity of TAL1 in T cell acute lymphoblastic leukemia (T-ALL) requires RBTN1 or -2 and induces TALLA1, a highly specific tumor marker of T-ALL". The Journal of Biological Chemistry. 272 (7): 4576–81. doi:10.1074/jbc.272.7.4576. PMID 9020185.
  38. ^ Albergaria A, Paredes J, Sousa B, Milanezi F, Carneiro V, Bastos J, et al. (2009). "Expression of FOXA1 and GATA-3 in breast cancer: the prognostic significance in hormone receptor-negative tumours". Breast Cancer Research. 11 (3): R40. doi:10.1186/bcr2327. PMC 2716509. PMID 19549328.
Attribution

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


Further reading

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