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'''T-cell leukemia homeobox protein 3''' is a [[protein]] that in humans is encoded by the ''TLX3'' [[gene]].<ref name="pmid11435718">{{cite journal | vauthors = Lee-Kirsch MA, Engel K, Paditz E, Rosen-Wolff A, Lee YA, Gahr M | title = Assignment of the human homeobox 11-like 2 gene (HOX11L2) to chromosome 5q34→q35 by radiation hybrid mapping | journal = Cytogenet Cell Genet | volume = 92 | issue = 3–4 | pages = 358 |date=Jul 2001 | pmid = 11435718 | pmc = | doi =10.1159/000056933 }}</ref><ref name="pmid11435716">{{cite journal | vauthors = Cinti R, Fava M, Sancandi M, Matera I, Ravazzolo R, Ceccherini I | title = Assignment of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome bands 11A4-A5 by in situ hybridization | journal = Cytogenet Cell Genet | volume = 92 | issue = 3–4 | pages = 354–5 |date=Jul 2001 | pmid = 11435716 | pmc = | doi =10.1159/000056931 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: TLX3 T-cell leukemia homeobox 3| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=30012| accessdate = }}</ref> | |||
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| summary_text = RNX (HOX11L2, TLX3) belongs to a family of orphan homeobox genes that encode DNA-binding nuclear transcription factors. Members of the HOX11 gene family are characterized by a threonine-47 replacing cytosine in the highly conserved homeodomain (Dear et al., 1993).[supplied by OMIM]<ref name="entrez" | | summary_text = RNX (HOX11L2, TLX3) belongs to a family of orphan homeobox genes that encode DNA-binding nuclear transcription factors. Members of the HOX11 gene family are characterized by a threonine-47 replacing cytosine in the highly conserved homeodomain (Dear et al., 1993).[supplied by OMIM]<ref name="entrez"/> | ||
}} | }} | ||
==References== | ==References== | ||
{{reflist | {{reflist}} | ||
==Further reading== | ==Further reading== | ||
{{refbegin | 2}} | {{refbegin | 2}} | ||
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| citations = | | citations = | ||
*{{cite journal | | *{{cite journal | vauthors=Dear TN, Sanchez-Garcia I, Rabbitts TH |title=The HOX11 gene encodes a DNA-binding nuclear transcription factor belonging to a distinct family of homeobox genes |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=90 |issue= 10 |pages= 4431–5 |year= 1993 |pmid= 8099440 |doi=10.1073/pnas.90.10.4431 | pmc=46525 }} | ||
*{{cite journal |vauthors=Bernard OA, Busson-LeConiat M, Ballerini P, etal |title=A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia |journal=Leukemia |volume=15 |issue= 10 |pages= 1495–504 |year= 2002 |pmid= 11587205 |doi=10.1038/sj.leu.2402249 }} | |||
*{{cite journal |vauthors=Ballerini P, Blaise A, Busson-Le Coniat M, etal |title=HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis |journal=Blood |volume=100 |issue= 3 |pages= 991–7 |year= 2002 |pmid= 12130513 |doi= 10.1182/blood-2001-11-0093 }} | |||
*{{cite journal | *{{cite journal |vauthors=Matera I, Bachetti T, Cinti R, etal |title=Mutational analysis of the RNX gene in congenital central hypoventilation syndrome |journal=Am. J. Med. Genet. |volume=113 |issue= 2 |pages= 178–82 |year= 2003 |pmid= 12407709 |doi= 10.1002/ajmg.10746 }} | ||
*{{cite journal | *{{cite journal |vauthors=Mauvieux L, Leymarie V, Helias C, etal |title=High incidence of Hox11L2 expression in children with T-ALL |journal=Leukemia |volume=16 |issue= 12 |pages= 2417–22 |year= 2003 |pmid= 12454747 |doi= 10.1038/sj.leu.2402709 }} | ||
*{{cite journal | *{{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 }} | ||
*{{cite journal | *{{cite journal |vauthors=Berger R, Dastugue N, Busson M, etal |title=t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Français de Cytogénétique Hématologique (GFCH) |journal=Leukemia |volume=17 |issue= 9 |pages= 1851–7 |year= 2003 |pmid= 12970786 |doi= 10.1038/sj.leu.2403061 }} | ||
*{{cite journal | *{{cite journal |vauthors=Cavé H, Suciu S, Preudhomme C, etal |title=Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: results of EORTC studies 58881 and 58951 |journal=Blood |volume=103 |issue= 2 |pages= 442–50 |year= 2004 |pmid= 14504110 |doi= 10.1182/blood-2003-05-1495 }} | ||
*{{cite journal | *{{cite journal |vauthors=Su XY, Busson M, Della Valle V, etal |title=Various types of rearrangements target TLX3 locus in T-cell acute lymphoblastic leukemia |journal=Genes Chromosomes Cancer |volume=41 |issue= 3 |pages= 243–9 |year= 2004 |pmid= 15334547 |doi= 10.1002/gcc.20088 }} | ||
*{{cite journal | *{{cite journal |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC) |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 }} | ||
*{{cite journal | *{{cite journal |vauthors=Ballerini P, Busson M, Fasola S, etal |title=NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significance |journal=Leukemia |volume=19 |issue= 3 |pages= 468–70 |year= 2005 |pmid= 15674415 |doi= 10.1038/sj.leu.2403654 }} | ||
*{{cite journal | *{{cite journal |vauthors=Gottardo NG, Jacoby PA, Sather HN, etal |title=Significance of HOX11L2/TLX3 expression in children with T-cell acute lymphoblastic leukemia treated on Children's Cancer Group protocols |journal=Leukemia |volume=19 |issue= 9 |pages= 1705–8 |year= 2005 |pmid= 15990867 |doi= 10.1038/sj.leu.2403834 }} | ||
*{{cite journal | *{{cite journal |vauthors=Borghini S, Vargiolu M, Di Duca M, etal |title=Nuclear factor Y drives basal transcription of the human TLX3, a gene overexpressed in T-cell acute lymphocytic leukemia |journal=Mol. Cancer Res. |volume=4 |issue= 9 |pages= 635–43 |year= 2006 |pmid= 16966433 |doi= 10.1158/1541-7786.MCR-05-0250 }} | ||
*{{cite journal | *{{cite journal |vauthors=Nagel S, Scherr M, Kel A, etal |title=Activation of TLX3 and NKX2-5 in t(5;14)(q35;q32) T-cell acute lymphoblastic leukemia by remote 3'-BCL11B enhancers and coregulation by PU.1 and HMGA1 |journal=Cancer Res. |volume=67 |issue= 4 |pages= 1461–71 |year= 2007 |pmid= 17308084 |doi= 10.1158/0008-5472.CAN-06-2615 }} | ||
*{{cite journal | |||
*{{cite journal | |||
}} | }} | ||
{{refend}} | {{refend}} | ||
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Latest revision as of 11:56, 15 September 2017
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T-cell leukemia homeobox protein 3 is a protein that in humans is encoded by the TLX3 gene.[1][2][3]
RNX (HOX11L2, TLX3) belongs to a family of orphan homeobox genes that encode DNA-binding nuclear transcription factors. Members of the HOX11 gene family are characterized by a threonine-47 replacing cytosine in the highly conserved homeodomain (Dear et al., 1993).[supplied by OMIM][3]
References
- ↑ Lee-Kirsch MA, Engel K, Paditz E, Rosen-Wolff A, Lee YA, Gahr M (Jul 2001). "Assignment of the human homeobox 11-like 2 gene (HOX11L2) to chromosome 5q34→q35 by radiation hybrid mapping". Cytogenet Cell Genet. 92 (3–4): 358. doi:10.1159/000056933. PMID 11435718.
- ↑ Cinti R, Fava M, Sancandi M, Matera I, Ravazzolo R, Ceccherini I (Jul 2001). "Assignment of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome bands 11A4-A5 by in situ hybridization". Cytogenet Cell Genet. 92 (3–4): 354–5. doi:10.1159/000056931. PMID 11435716.
- ↑ 3.0 3.1 "Entrez Gene: TLX3 T-cell leukemia homeobox 3".
Further reading
- Dear TN, Sanchez-Garcia I, Rabbitts TH (1993). "The HOX11 gene encodes a DNA-binding nuclear transcription factor belonging to a distinct family of homeobox genes". Proc. Natl. Acad. Sci. U.S.A. 90 (10): 4431–5. doi:10.1073/pnas.90.10.4431. PMC 46525. PMID 8099440.
- Bernard OA, Busson-LeConiat M, Ballerini P, et al. (2002). "A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia". Leukemia. 15 (10): 1495–504. doi:10.1038/sj.leu.2402249. PMID 11587205.
- Ballerini P, Blaise A, Busson-Le Coniat M, et al. (2002). "HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis". Blood. 100 (3): 991–7. doi:10.1182/blood-2001-11-0093. PMID 12130513.
- Matera I, Bachetti T, Cinti R, et al. (2003). "Mutational analysis of the RNX gene in congenital central hypoventilation syndrome". Am. J. Med. Genet. 113 (2): 178–82. doi:10.1002/ajmg.10746. PMID 12407709.
- Mauvieux L, Leymarie V, Helias C, et al. (2003). "High incidence of Hox11L2 expression in children with T-ALL". Leukemia. 16 (12): 2417–22. doi:10.1038/sj.leu.2402709. PMID 12454747.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Berger R, Dastugue N, Busson M, et al. (2003). "t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Français de Cytogénétique Hématologique (GFCH)". Leukemia. 17 (9): 1851–7. doi:10.1038/sj.leu.2403061. PMID 12970786.
- Cavé H, Suciu S, Preudhomme C, et al. (2004). "Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: results of EORTC studies 58881 and 58951". Blood. 103 (2): 442–50. doi:10.1182/blood-2003-05-1495. PMID 14504110.
- Su XY, Busson M, Della Valle V, et al. (2004). "Various types of rearrangements target TLX3 locus in T-cell acute lymphoblastic leukemia". Genes Chromosomes Cancer. 41 (3): 243–9. doi:10.1002/gcc.20088. PMID 15334547.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Ballerini P, Busson M, Fasola S, et al. (2005). "NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significance". Leukemia. 19 (3): 468–70. doi:10.1038/sj.leu.2403654. PMID 15674415.
- Gottardo NG, Jacoby PA, Sather HN, et al. (2005). "Significance of HOX11L2/TLX3 expression in children with T-cell acute lymphoblastic leukemia treated on Children's Cancer Group protocols". Leukemia. 19 (9): 1705–8. doi:10.1038/sj.leu.2403834. PMID 15990867.
- Borghini S, Vargiolu M, Di Duca M, et al. (2006). "Nuclear factor Y drives basal transcription of the human TLX3, a gene overexpressed in T-cell acute lymphocytic leukemia". Mol. Cancer Res. 4 (9): 635–43. doi:10.1158/1541-7786.MCR-05-0250. PMID 16966433.
- Nagel S, Scherr M, Kel A, et al. (2007). "Activation of TLX3 and NKX2-5 in t(5;14)(q35;q32) T-cell acute lymphoblastic leukemia by remote 3'-BCL11B enhancers and coregulation by PU.1 and HMGA1". Cancer Res. 67 (4): 1461–71. doi:10.1158/0008-5472.CAN-06-2615. PMID 17308084.
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