{{short description|Transcription factor gene involved in the urogenital system}} {{cs1 config|name-list-style=vanc}}
{{Infobox_gene}} '''Wilms tumor protein''' (WT33) is a protein that in humans is encoded by the ''WT1'' gene on chromosome 11p.<ref name="pmid2406020">{{cite journal | vauthors = Burgin AB, Parodos K, Lane DJ, Pace NR | title = The excision of intervening sequences from Salmonella 23S ribosomal RNA | journal = Cell | volume = 60 | issue = 3 | pages = 405–14 | date = February 1990 | pmid = 2406020 | doi = 10.1016/0092-8674(90)90592-3 | s2cid = 39909491 }}</ref><ref name="pmid2154335">{{cite journal | vauthors = Call KM, Glaser T, Ito CY, Buckler AJ, Pelletier J, Haber DA, Rose EA, Kral A, Yeger H, Lewis WH | title = Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus | journal = Cell | volume = 60 | issue = 3 | pages = 509–20 | date = February 1990 | pmid = 2154335 | doi = 10.1016/0092-8674(90)90601-A | s2cid = 29092372 }}</ref><ref name="pmid2154702">{{cite journal | vauthors = Gessler M, Poustka A, Cavenee W, Neve RL, Orkin SH, Bruns GA | title = Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping | journal = Nature | volume = 343 | issue = 6260 | pages = 774–8 | date = February 1990 | pmid = 2154702 | doi = 10.1038/343774a0 | bibcode = 1990Natur.343..774G | s2cid = 4235306 | url = https://opus.bibliothek.uni-wuerzburg.de/files/2573/Gessler_Homozygous.pdf }}</ref><ref name="pmid2173145">{{cite journal | vauthors = Huang A, Campbell CE, Bonetta L, McAndrews-Hill MS, Chilton-MacNeill S, Coppes MJ, Law DJ, Feinberg AP, Yeger H, Williams BR | title = Tissue, developmental, and tumor-specific expression of divergent transcripts in Wilms tumor | journal = Science | volume = 250 | issue = 4983 | pages = 991–4 | date = November 1990 | pmid = 2173145 | doi = 10.1126/science.2173145 | bibcode = 1990Sci...250..991H }}</ref>
== Function ==
This gene encodes a transcription factor that contains four zinc finger motifs at the C-terminus and a proline / glutamine-rich DNA-binding domain at the N-terminus. It has an essential role in the normal development of the urogenital system, and it is mutated in a subset of patients with Wilms' tumor, the gene's namesake. Multiple transcript variants, resulting from alternative splicing at two coding exons, have been well characterized. There is also evidence for the use of non-AUG (CUG) translation initiation site upstream of, and in-frame with the first AUG, leading to additional isoforms.<ref>{{cite web | title = Entrez Gene: WT1 Wilms tumor 1| url = https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=7490}}</ref>
== Structure ==
{{Infobox protein family | Symbol = WT1 | Name = WT1 | image = | width = | caption = structure of the wilms tumor suppressor protein zinc finger domain bound to dna | Pfam = PF02165 | Pfam_clan = | InterPro = IPR000976 | SMART = | PROSITE = | MEROPS = | SCOP = | TCDB = | OPM family = | OPM protein = | CAZy = | CDD = | align = left }} The WT1 gene product shows similarity to the zinc fingers of the mammalian growth regulated early growth response protein 1 (EGR1) and (EGR2) proteins.<ref name="pmid17634147">{{cite journal | vauthors = Han Y, San-Marina S, Yang L, Khoury H, Minden MD | title = The zinc finger domain of Wilms' tumor 1 suppressor gene (WT1) behaves as a dominant negative, leading to abrogation of WT1 oncogenic potential in breast cancer cells | journal = Breast Cancer Research | volume = 9 | issue = 4 | pages = R43 | year = 2007 | pmid = 17634147 | pmc = 2206716 | doi = 10.1186/bcr1743 | doi-access = free }}</ref> {{clear|left}}
== Clinical significance ==
''Mutations of Wilms' tumor suppressor gene1'' (WT1) are associated with embryonic malignancy of the kidney, affecting around 1-9 in 100,000 infants.<ref>{{Cite web|url=https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=654|title=Orphanet: Nephroblastoma |website=www.orpha.net|access-date=2019-05-06}}</ref> It occurs in both sporadic and hereditary forms. Inactivation of WT1 causes Wilms tumour, and Denys-Drash syndrome (DDS), leading to nephropathy and genital abnormalities. The WT1 protein has been found to bind a host of cellular factors, e.g. p53, a known tumor suppressor.<ref name="pmid2154702" /><ref name="pmid8393820">{{cite journal | vauthors = Rauscher FJ | title = The WT1 Wilms' tumor gene product: a developmentally regulated transcription factor in the kidney that functions as a tumor suppressor | journal = FASEB Journal | volume = 7 | issue = 10 | pages = 896–903 | date = July 1993 | pmid = 8393820 | doi = 10.1096/fasebj.7.10.8393820| doi-access = free | s2cid = 221754031 }}</ref><ref name="pmid1671709">{{cite journal | vauthors = Buckler AJ, Pelletier J, Haber DA, Glaser T, Housman DE | title = Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development | journal = Molecular and Cellular Biology | volume = 11 | issue = 3 | pages = 1707–12 | date = March 1991 | pmid = 1671709 | pmc = 369476 | doi = 10.1128/mcb.11.3.1707 }}</ref><ref name="pmid1317572">{{cite journal | vauthors = Little MH, Prosser J, Condie A, Smith PJ, Van Heyningen V, Hastie ND | title = Zinc finger point mutations within the WT1 gene in Wilms tumor patients | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 89 | issue = 11 | pages = 4791–5 | date = June 1992 | pmid = 1317572 | pmc = 49173 | doi = 10.1073/pnas.89.11.4791 | bibcode = 1992PNAS...89.4791L | doi-access = free }}</ref> Despite the name, WT1 mutation is found in only about 5-10% of Wilms Tumor cases.<ref>{{cite journal | vauthors = Davidoff AM | title = Wilms tumor | journal = Advances in Pediatrics | volume = 59 | issue = 1 | pages = 247–267 | year = 2012 | pmid = 22789581 | pmc = 3589819 | doi = 10.1016/j.yapd.2012.04.001 }}</ref> Some other genes associated with this disease are BRCA2 and GPC3.
WT1 is mutated in a mutually exclusive manner with TET2, IDH1, and IDH2 in acute myeloid leukemia.<ref name="pmid25482556">{{cite journal | vauthors = Rampal R, Alkalin A, Madzo J, Vasanthakumar A, Pronier E, Patel J, Li Y, Ahn J, Abdel-Wahab O, Shih A, Lu C, Ward PS, Tsai JJ, Hricik T, Tosello V, Tallman JE, Zhao X, Daniels D, Dai Q, Ciminio L, Aifantis I, He C, Fuks F, Tallman MS, Ferrando A, Nimer S, Paietta E, Thompson CB, Licht JD, Mason CE, Godley LA, Melnick A, Figueroa ME, Levine RL | title = DNA hydroxymethylation profiling reveals that WT1 mutations result in loss of TET2 function in acute myeloid leukemia | journal = Cell Reports | volume = 9 | issue = 5 | pages = 1841–1855 | date = December 2014 | pmid = 25482556 | pmc = 4267494 | doi = 10.1016/j.celrep.2014.11.004 }}</ref> TET2 can be recruited by WT1 to its target genes and activates WT1-target genes by converting 5mC into 5hmC residues at the genes' promoters,<ref name="pmid25601757">{{cite journal | vauthors = Wang Y, Xiao M, Chen X, Chen L, Xu Y, Lv L, Wang P, Yang H, Ma S, Lin H, Jiao B, Ren R, Ye D, Guan KL, Xiong Y | title = WT1 recruits TET2 to regulate its target gene expression and suppress leukemia cell proliferation | journal = Molecular Cell | volume = 57 | issue = 4 | pages = 662–673 | date = February 2015 | pmid = 25601757 | pmc = 4336627 | doi = 10.1016/j.molcel.2014.12.023 }}</ref> representing an important feature of a new regulatory WIT pathway linked to the development of AML.<ref name="pmid25699704">{{cite journal | vauthors = Sardina JL, Graf T | title = A new path to leukemia with WIT | journal = Molecular Cell | volume = 57 | issue = 4 | pages = 573–574 | date = February 2015 | pmid = 25699704 | doi = 10.1016/j.molcel.2015.02.005 | doi-access = free }}</ref>
The serine protease HtrA2 binds to WT1 and it cleaves WT1 at multiple sites following the treatment with cytotoxic drugs.<ref name="pmid20122396">{{cite journal | vauthors = Essafi A, Hastie ND | title = WT1 the oncogene: a tale of death and HtrA | journal = Molecular Cell | volume = 37 | issue = 2 | pages = 153–5 | date = January 2010 | pmid = 20122396 | doi = 10.1016/j.molcel.2010.01.010 | doi-access = free }}</ref><ref name="pmid20122399">{{cite journal | vauthors = Hartkamp J, Carpenter B, Roberts SG | title = The Wilms' tumor suppressor protein WT1 is processed by the serine protease HtrA2/Omi | journal = Molecular Cell | volume = 37 | issue = 2 | pages = 159–71 | date = January 2010 | pmid = 20122399 | pmc = 2815029 | doi = 10.1016/j.molcel.2009.12.023 }}</ref>
Using immunohistochemistry, WT1 protein can be demonstrated in the cell nuclei of 75% of mesotheliomas and in 93% of ovarian serous carcinomas, as well as in benign mesothelium and fallopian tube epithelium. This allows these tumours to be distinguished from other, similar, cancers, such as adenocarcinoma. Antibodies to the WT1 protein, however, also frequently cross-react with cytoplasmic proteins in a variety of benign and malignant cells, so that only nuclear staining can be considered diagnostic.<ref name=Leong>{{cite book | vauthors = Leong AS, Cooper K, Leong FJ | year = 2003 | title = Manual of Diagnostic Cytology | edition = 2 | publisher = Greenwich Medical Media, Ltd. | pages = 447–448 | isbn = 978-1-84110-100-2 }}</ref>
Mutation in WT1 causes predisposition to hernias.<ref name="urlA genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia - PubMed">{{cite journal | vauthors = Jorgenson E, Makki N, Shen L, Chen DC, Tian C, Eckalbar WL, Hinds D, Ahituv N, Avins A | title = A genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia | journal = Nature Communications | volume = 6 | article-number = 10130 | date = December 2015 | pmid = 26686553 | pmc = 4703831 | doi = 10.1038/ncomms10130 | bibcode = 2015NatCo...610130J }}</ref>
===As a drug target===
A vaccine that induces an acquired immune response against WT1 is in clinical trials for various cancers.<ref name=Sellas2016-05>{{Cite web |url=http://sellaslifesciences.com/2016/05/sellas-life-sciences-announces-positive-wt1-cancer-vaccine-galinpepimut-s-clinical-results-at-the-13th-international-conference-of-the-international-mesothelioma-interest-group-imig/ |title=SELLAS Life Sciences Announces Positive WT1 Cancer Vaccine (galinpepimut-S) Clinical Results at the 13th International Conference of the International Mesothelioma Interest Group (iMig) |access-date=2016-05-08 |archive-date=2016-06-04 |archive-url=https://web.archive.org/web/20160604123918/http://sellaslifesciences.com/2016/05/sellas-life-sciences-announces-positive-wt1-cancer-vaccine-galinpepimut-s-clinical-results-at-the-13th-international-conference-of-the-international-mesothelioma-interest-group-imig/ }}</ref><ref name=mymeso2016>{{usurped|1=[https://web.archive.org/web/20160603153713/http://www.mymeso.org/2016/04/08/pleural-mesothelioma-wt1-vaccine-is-renamed-galinpepimut-s/ Pleural mesothelioma WT1 vaccine is renamed "galinpepimut-S"]}}</ref><ref name=Oka2006>{{cite journal | vauthors = Oka Y, Tsuboi A, Kawakami M, Elisseeva OA, Nakajima H, Udaka K, Kawase I, Oji Y, Sugiyama H | title = Development of WT1 peptide cancer vaccine against hematopoietic malignancies and solid cancers | journal = Current Medicinal Chemistry | volume = 13 | issue = 20 | pages = 2345–52 | pmid = 16918359 | year = 2006 | doi = 10.2174/092986706777935104 }}</ref> T cell therapies (TCR-T) are also being tested in clinical trials for leukemia.<ref>{{cite journal | vauthors = Chapuis AG, Egan DN, Bar M, Schmitt TM, McAfee MS, Paulson KG, Voillet V, Gottardo R, Ragnarsson GB, Bleakley M, Yeung CC, Muhlhauser P, Nguyen HN, Kropp LA, Castelli L, Wagener F, Hunter D, Lindberg M, Cohen K, Seese A, McElrath MJ, Duerkopp N, Gooley TA, Greenberg PD | display-authors = 6 | title = T cell receptor gene therapy targeting WT1 prevents acute myeloid leukemia relapse post-transplant | journal = Nature Medicine | volume = 25 | issue = 7 | pages = 1064–1072 | date = July 2019 | pmid = 31235963 | pmc = 6982533 | doi = 10.1038/s41591-019-0472-9 | doi-access = free }}</ref><ref>{{cite journal | vauthors = Tawara I, Kageyama S, Miyahara Y, Fujiwara H, Nishida T, Akatsuka Y, Ikeda H, Tanimoto K, Terakura S, Murata M, Inaguma Y, Masuya M, Inoue N, Kidokoro T, Okamoto S, Tomura D, Chono H, Nukaya I, Mineno J, Naoe T, Emi N, Yasukawa M, Katayama N, Shiku H | display-authors = 6 | title = Safety and persistence of WT1-specific T-cell receptor gene-transduced lymphocytes in patients with AML and MDS | journal = Blood | volume = 130 | issue = 18 | pages = 1985–1994 | date = November 2017 | pmid = 28860210 | doi = 10.1182/blood-2017-06-791202 | doi-access = free }}</ref>
=== Disease monitoring === WT1 gene is overexpressed in case of hematological malignancies. This fact is widely used for disease monitoring - evaluations of treatment success, as well as relapse or remission post-treatment checks. Preferably quantitative polymerase chain reaction (qPCR) is used to establish the levels of WT1 expression. The rising level of WT1 expression is significantly connected with disease progression and relapse of the proliferative disorder.<ref>{{cite journal | vauthors = Candoni A, Toffoletti E, Gallina R, Simeone E, Chiozzotto M, Volpetti S, Fanin R | title = Monitoring of minimal residual disease by quantitative WT1 gene expression following reduced intensity conditioning allogeneic stem cell transplantation in acute myeloid leukemia | journal = Clinical Transplantation | volume = 25 | issue = 2 | pages = 308–16 | date = March 2011 | pmid = 20412098 | doi = 10.1111/j.1399-0012.2010.01251.x | s2cid = 6677442 | doi-access = free | hdl = 11380/1294142 | hdl-access = free }}</ref> WT1 as a marker is used as a "golden standard" for monitoring of acute myeloid leukemia, however other hematological malignancies such as chronic myeloid leukemia or myeloproliferative syndrome can manifest with overexpressed WT1 and for in specific cases WT1 monitoring can be used even in patients diagnosed with those types of cancer.<ref name="Sugiyama">{{cite journal | vauthors = Sugiyama H | title = WT1 (Wilms' tumor gene 1): biology and cancer immunotherapy | journal = Japanese Journal of Clinical Oncology | volume = 40 | issue = 5 | pages = 377–87 | date = May 2010 | pmid = 20395243 | doi = 10.1093/jjco/hyp194 | doi-access = free }}</ref>
== Interactions ==
WT1 has been shown to interact with TET2,<ref name="pmid25601757"/> U2AF2,<ref name="pmid9784496">{{cite journal | vauthors = Davies RC, Calvio C, Bratt E, Larsson SH, Lamond AI, Hastie ND | title = WT1 interacts with the splicing factor U2AF65 in an isoform-dependent manner and can be incorporated into spliceosomes | journal = Genes & Development | volume = 12 | issue = 20 | pages = 3217–25 | date = October 1998 | pmid = 9784496 | pmc = 317218 | doi = 10.1101/gad.12.20.3217 }}</ref> PAWR,<ref name="pmid8943350">{{cite journal | vauthors = Johnstone RW, See RH, Sells SF, Wang J, Muthukkumar S, Englert C, Haber DA, Licht JD, Sugrue SP, Roberts T, Rangnekar VM, Shi Y | title = A novel repressor, par-4, modulates transcription and growth suppression functions of the Wilms' tumor suppressor WT1 | journal = Molecular and Cellular Biology | volume = 16 | issue = 12 | pages = 6945–56 | date = December 1996 | pmid = 8943350 | pmc = 231698 | doi = 10.1128/mcb.16.12.6945 }}</ref> UBE2I<ref name="pmid8798754">{{cite journal | vauthors = Wang ZY, Qiu QQ, Seufert W, Taguchi T, Testa JR, Whitmore SA, Callen DF, Welsh D, Shenk T, Deuel TF | title = Molecular cloning of the cDNA and chromosome localization of the gene for human ubiquitin-conjugating enzyme 9 | journal = The Journal of Biological Chemistry | volume = 271 | issue = 40 | pages = 24811–6 | date = October 1996 | pmid = 8798754 | doi = 10.1074/jbc.271.40.24811 | doi-access = free }}</ref> and WTAP.<ref name="pmid11001926">{{cite journal | vauthors = Little NA, Hastie ND, Davies RC | title = Identification of WTAP, a novel Wilms' tumour 1-associating protein | journal = Human Molecular Genetics | volume = 9 | issue = 15 | pages = 2231–9 | date = September 2000 | pmid = 11001926 | doi = 10.1093/oxfordjournals.hmg.a018914 | doi-access = free }}</ref> In combination with Cited2 activates WT1 the Steroidogenic factor 1<ref name=pmid17537799>{{cite journal | vauthors = Val P, Martinez-Barbera JP, Swain A | title = Adrenal development is initiated by Cited2 and Wt1 through modulation of Sf-1 dosage | journal = Development | volume = 134 | issue = 12 | pages = 2349–58 | date = June 2007 | pmid = 17537799 | doi = 10.1242/dev.004390 | doi-access = free }}</ref>
== RNA editing ==
There is some evidence for RNA editing of human WT1 mRNA. As with alternative splicing of the gene RNA editing increases the number of isoforms of this protein.<ref name="pmid7926762">{{cite journal | vauthors = Sharma PM, Bowman M, Madden SL, Rauscher FJ, Sukumar S | title = RNA editing in the Wilms' tumor susceptibility gene, WT1 | journal = Genes & Development | volume = 8 | issue = 6 | pages = 720–31 | date = March 1994 | pmid = 7926762 | doi = 10.1101/gad.8.6.720 | doi-access = free }}</ref><ref name="pmid12665546">{{cite journal | vauthors = Wagner KD, Wagner N, Schedl A | title = The complex life of WT1 | journal = Journal of Cell Science | volume = 116 | issue = Pt 9 | pages = 1653–8 | date = May 2003 | pmid = 12665546 | doi = 10.1242/jcs.00405 | doi-access = free }}</ref>
Editing is tissue specific and developmentally regulated. Editing shown to be restricted in testis and kidney in the rat.<ref name="pmid7926762"/> Editing of this gene product has been found to occur in mice and rats as well as humans.<ref name="pmid7926762"/><ref name="pmid11065340">{{cite journal | vauthors = Mrowka C, Schedl A | title = Wilms' tumor suppressor gene WT1: from structure to renal pathophysiologic features | journal = Journal of the American Society of Nephrology | volume = 11 | pages = S106–15 | date = November 2000 | issue = Suppl 16 | doi = 10.1681/ASN.V11suppl_2s106 | pmid = 11065340 | url = http://jasn.asnjournals.org/cgi/pmidlookup?view=long&pmid=11065340 | doi-access = free | url-access = subscription }}</ref>
=== Editing type ===
The editing site is found at nucleotide position 839 found in exon 6 of the gene. It causes a codon change from a Proline codon (CCC) to a Leucine codon (CUC).<ref name="pmid7926762"/>
The type of editing is a uridine to cytidine (U to C) base change. The editing reaction is thought to be an amidation of uridine which converts it to a cytidine. The relevance of this editing is unknown as is the enzyme responsible for this editing. The region where editing occurs like that of other editing sites, e.g., ApoB mRNA editing is conserved. Mice, rats and humans have conserved sequences flanking the editing site consisting of 10 nucleotides before the editing site and four after the site.<ref name="pmid7926762"/>
=== Effects of editing ===
RNA editing results in an alternative amino acid being translated.<ref name="pmid7926762"/> The changes in amino acid occur in a region identified as a domain involved in transcription activation function.<ref name="pmid8486616">{{cite journal | vauthors = Wang ZY, Qiu QQ, Deuel TF | title = The Wilms' tumor gene product WT1 activates or suppresses transcription through separate functional domains | journal = The Journal of Biological Chemistry | volume = 268 | issue = 13 | pages = 9172–5 | date = May 1993 | doi = 10.1016/S0021-9258(18)98329-8 | pmid = 8486616 | url = http://www.jbc.org/cgi/pmidlookup?view=long&pmid=8486616 | doi-access = free }}</ref>
Editing has been shown to decrease repressive regulation of transcription of growth promoting genes ''in vitro'' compared to the non edited protein. Although the physiological role of editing has yet to be determined, suggestions have been made that editing may play a role in the pathogenesis of Wilms tumour.<ref name="pmid11065340"/>
== Experimental models == WT1 gene can be found as well in the genome of mice. The mouse model with a WT1 knock-out shows symptoms corresponding to human pathophysiology. The mice were observed to have defects of urogenital tract similar to cases patients when WT1 signalling has been malfunctioning.<ref name="Sugiyama" /> The mouse had absent kidneys as their development failed during embryonic stages. This suggests that WT1 is unconditionally required for a proper kidney formation and development.<ref name="Ozdemir Hohenstein">{{cite journal | vauthors = Ozdemir DD, Hohenstein P | title = Wt1 in the kidney--a tale in mouse models | journal = Pediatric Nephrology | volume = 29 | issue = 4 | pages = 687–93 | date = April 2014 | pmid = 24240471 | doi = 10.1007/s00467-013-2673-7 | s2cid = 2019375 }}</ref>
Apart from that, the WT1 knock-out mice lacked several types of glands, such as gonads or adrenal glands. The effect of the knock-out was as well visible on heart and blood circulation - several abnormalities concerning heart and diaphragm, as well as troubles with swelling and lymph circulation were described. Due to those defects, the mouse died before it was even born.<ref name="Ozdemir Hohenstein" />
Mouse model is used to study some specific disorder connected with WT1 expression, too, such as acute myeloid leukemia.<ref name="pmid10942395">{{cite journal | vauthors = Gaiger A, Reese V, Disis ML, Cheever MA | title = Immunity to WT1 in the animal model and in patients with acute myeloid leukemia | journal = Blood | volume = 96 | issue = 4 | pages = 1480–9 | date = August 2000 | pmid = 10942395 | doi = 10.1182/blood.V96.4.1480| doi-access = free }}</ref> To examine the expression levels and localisation of WT1, a mouse model using WT1-GFP (green fluorescent protein) knock-in has been made. This model showed, that WT1 is significantly overexpressed in leukemic cells compared to none or minor expression in normal untransformed cells from bone marrow, either hematopoietic stem cells or hematopoietic progenitors and precursors.<ref>{{cite journal | vauthors = Hosen N, Shirakata T, Nishida S, Yanagihara M, Tsuboi A, Kawakami M, Oji Y, Oka Y, Okabe M, Tan B, Sugiyama H, Weissman IL | title = The Wilms' tumor gene WT1-GFP knock-in mouse reveals the dynamic regulation of WT1 expression in normal and leukemic hematopoiesis | journal = Leukemia | volume = 21 | issue = 8 | pages = 1783–91 | date = August 2007 | pmid = 17525726 | doi = 10.1038/sj.leu.2404752 | doi-access = free }}</ref>
== References == {{Reflist}}
== Further reading == {{refbegin|30em}} * {{cite journal | vauthors = Haber DA, Buckler AJ | title = WT1: a novel tumor suppressor gene inactivated in Wilms' tumor | journal = The New Biologist | volume = 4 | issue = 2 | pages = 97–106 | date = February 1992 | pmid = 1313285 }} * {{cite journal | vauthors = Rauscher FJ | title = The WT1 Wilms tumor gene product: a developmentally regulated transcription factor in the kidney that functions as a tumor suppressor | journal = FASEB Journal | volume = 7 | issue = 10 | pages = 896–903 | date = July 1993 | pmid = 8393820 | doi = 10.1096/fasebj.7.10.8393820| doi-access = free | s2cid = 221754031 }} * {{cite journal | vauthors = Lee SB, Haber DA | title = Wilms tumor and the WT1 gene | journal = Experimental Cell Research | volume = 264 | issue = 1 | pages = 74–99 | date = March 2001 | pmid = 11237525 | doi = 10.1006/excr.2000.5131 }} * {{cite journal | vauthors = Scharnhorst V, van der Eb AJ, Jochemsen AG | title = WT1 proteins: functions in growth and differentiation | journal = Gene | volume = 273 | issue = 2 | pages = 141–61 | date = August 2001 | pmid = 11595161 | doi = 10.1016/S0378-1119(01)00593-5 | s2cid = 43456904 }} * {{cite journal | vauthors = Lim HN, Hughes IA, Hawkins JR | title = Clinical and molecular evidence for the role of androgens and WT1 in testis descent | journal = Molecular and Cellular Endocrinology | volume = 185 | issue = 1–2 | pages = 43–50 | date = December 2001 | pmid = 11738793 | doi = 10.1016/S0303-7207(01)00631-1 | s2cid = 44309863 }} * {{cite journal | vauthors = Heathcott RW, Morison IM, Gubler MC, Corbett R, Reeve AE | title = A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X | journal = Human Mutation | volume = 19 | issue = 4 | page = 462 | date = April 2002 | pmid = 11933209 | doi = 10.1002/humu.9031 | s2cid = 39999285 | doi-access = free }} * {{cite journal | vauthors = Wagner KD, Wagner N, Schedl A | title = The complex life of WT1 | journal = Journal of Cell Science | volume = 116 | issue = Pt 9 | pages = 1653–8 | date = May 2003 | pmid = 12665546 | doi = 10.1242/jcs.00405 | doi-access = free }} * {{cite journal | vauthors = Amini Nik S, Hohenstein P, Jadidizadeh A, Van Dam K, Bastidas A, Berry RL, Patek CE, Van der Schueren B, Cassiman JJ, Tejpar S | title = Upregulation of Wilms' tumor gene 1 (WT1) in desmoid tumors | journal = International Journal of Cancer | volume = 114 | issue = 2 | pages = 202–8 | date = March 2005 | pmid = 15540161 | doi = 10.1002/ijc.20717 | s2cid = 26931961 | doi-access = free }} * {{cite journal | vauthors = Niaudet P, Gubler MC | title = WT1 and glomerular diseases | journal = Pediatric Nephrology | volume = 21 | issue = 11 | pages = 1653–60 | date = November 2006 | pmid = 16927106 | doi = 10.1007/s00467-006-0208-1 | s2cid = 39936917 }} * {{cite journal | vauthors = Coosemans A, Nik SA, Caluwaerts S, Lambin S, Verbist G, Van Bree R, Schelfhout V, de Jonge E, Dalle I, Jacomen G, Cassiman JJ, Moerman P, Vergote I, Amant F | title = Upregulation of Wilms' tumour gene 1 (WT1) in uterine sarcomas | journal = European Journal of Cancer | volume = 43 | issue = 10 | pages = 1630–7 | date = July 2007 | pmid = 17531467 | doi = 10.1016/j.ejca.2007.04.008 | url = https://lirias.kuleuven.be/handle/123456789/157575 | url-access = subscription }} * {{cite journal | vauthors = Hohenstein P, Hastie ND | title = The many facets of the Wilms' tumour gene, WT1 | journal = Human Molecular Genetics | volume = 15 Spec No 2 | pages = R196–201 | date = October 2006 | pmid = 16987884 | doi = 10.1093/hmg/ddl196 | s2cid = 6523548 | doi-access = free }} {{refend}}
== External links == * [https://www.ncbi.nlm.nih.gov/books/NBK1360/ GeneReviews/NCBI/NIH/UW entry on Aniridia] * [https://omim.org/search?index=entry&start=1&limit=10&search=106210+194070+194072+607102+607108+106210+194070+194072+607102+607108&sort=score+desc&field=number OMIM entries on Aniridia] * [https://www.ncbi.nlm.nih.gov/books/NBK1294/ GeneReviews/NIH/NCBI/UW entry on Wilms Tumor Overview] * {{PDBe-KB2|P19544|Wilms tumor protein}}
{{PDB Gallery|geneid=7490}} {{Tumor suppressor genes}} {{Transcription factors|g2}}