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Volumn 74, Issue 2, 2008, Pages 145-147

HNF1β and defective nephrogenesis: A role for interacting partners?

Author keywords

[No Author keywords available]

Indexed keywords

HEPATOCYTE NUCLEAR FACTOR 1BETA; SUPPRESSOR OF CYTOKINE SIGNALING 3;

EID: 46249121022     PISSN: 00852538     EISSN: 15231755     Source Type: Journal    
DOI: 10.1038/ki.2008.250     Document Type: Note
Times cited : (7)

References (21)
  • 1
    • 0025775278 scopus 로고
    • vHNF1 is a homeoprotein that activates transcription and forms heterodimers with HNF1
    • Rey-Campos J, Chouard T, Yaniv M et al. vHNF1 is a homeoprotein that activates transcription and forms heterodimers with HNF1. EMBO J 1991; 10: 1445-1457.
    • (1991) EMBO J , vol.10 , pp. 1445-1457
    • Rey-Campos, J.1    Chouard, T.2    Yaniv, M.3
  • 2
    • 0025853775 scopus 로고
    • LFB3, a heterodimer-forming homeoprotein of the LFB1 family, is expressed in specialized epithelia
    • De Simone V, De Magistris L, Lazzaro D et al. LFB3, a heterodimer-forming homeoprotein of the LFB1 family, is expressed in specialized epithelia. EMBO J 1991; 10: 1435-1443.
    • (1991) EMBO J , vol.10 , pp. 1435-1443
    • De Simone, V.1    De Magistris, L.2    Lazzaro, D.3
  • 3
    • 0032727268 scopus 로고    scopus 로고
    • Variant hepatocyte nuclear factor 1 is required for visceral endoderm specification
    • Barbacci E, Reber M, Ott MO et al. Variant hepatocyte nuclear factor 1 is required for visceral endoderm specification. Development 1999; 126: 4795-4805.
    • (1999) Development , vol.126 , pp. 4795-4805
    • Barbacci, E.1    Reber, M.2    Ott, M.O.3
  • 4
    • 0344771681 scopus 로고    scopus 로고
    • Essential role for the homeoprotein vHNF1/HNF1beta in visceral endoderm differentiation
    • Coffinier C, Thepot D, Babinet C et al. Essential role for the homeoprotein vHNF1/HNF1beta in visceral endoderm differentiation. Development 1999; 126: 4785-4794.
    • (1999) Development , vol.126 , pp. 4785-4794
    • Coffinier, C.1    Thepot, D.2    Babinet, C.3
  • 5
    • 0036336513 scopus 로고    scopus 로고
    • Bile system morphogenesis defects and liver dysfunction upon targeted deletion of HNF1beta
    • Coffinier C, Gresh L, Fiette L et al. Bile system morphogenesis defects and liver dysfunction upon targeted deletion of HNF1beta. Development 2002; 129: 1829-1838.
    • (2002) Development , vol.129 , pp. 1829-1838
    • Coffinier, C.1    Gresh, L.2    Fiette, L.3
  • 6
    • 2342508500 scopus 로고    scopus 로고
    • A transcriptional network in polycystic kidney disease
    • Gresh L, Fischer E, Reimann A et al. A transcriptional network in polycystic kidney disease. EMBO J 2004; 23: 1657-1668.
    • (2004) EMBO J , vol.23 , pp. 1657-1668
    • Gresh, L.1    Fischer, E.2    Reimann, A.3
  • 7
    • 2142659368 scopus 로고    scopus 로고
    • Mutation of hepatocyte nuclear factor-1beta inhibits Pkhd1 gene expression and produces renal cysts in mice
    • Hiesberger T, Bai Y, Shao X et al. Mutation of hepatocyte nuclear factor-1beta inhibits Pkhd1 gene expression and produces renal cysts in mice. J Clin Invest 2004; 113: 814-825.
    • (2004) J Clin Invest , vol.113 , pp. 814-825
    • Hiesberger, T.1    Bai, Y.2    Shao, X.3
  • 8
    • 29444450890 scopus 로고    scopus 로고
    • Defective planar cell polarity in polycystic kidney disease
    • Fischer E, Legue E, Doyen A et al. Defective planar cell polarity in polycystic kidney disease. Nat Genet 2006; 38: 21-23.
    • (2006) Nat Genet , vol.38 , pp. 21-23
    • Fischer, E.1    Legue, E.2    Doyen, A.3
  • 9
    • 44349116202 scopus 로고    scopus 로고
    • Acute kidney injury and aberrant planar cell polarity induce cyst formation in mice lacking renal cilia
    • publication, 9 February, doi:10.1093/hmg/ddn045
    • Patel V, Li L, Cobo-Stark P et al. Acute kidney injury and aberrant planar cell polarity induce cyst formation in mice lacking renal cilia. Hum Mol Genet advance online publication, 9 February 2008, doi:10.1093/hmg/ddn045.
    • (2008) Hum Mol Genet advance online
    • Patel, V.1    Li, L.2    Cobo-Stark, P.3
  • 10
    • 0037884961 scopus 로고    scopus 로고
    • Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease
    • Lin F, Hiesberger T, Cordes K et al. Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease. Proc Natl Acad Sci USA 2003; 100: 5286-5291.
    • (2003) Proc Natl Acad Sci USA , vol.100 , pp. 5286-5291
    • Lin, F.1    Hiesberger, T.2    Cordes, K.3
  • 11
    • 38049144145 scopus 로고    scopus 로고
    • Mutations of HNF-1beta inhibit epithelial morphogenesis through dysregulation of SOCS-3
    • Ma Z, Gong Y, Patel V et al. Mutations of HNF-1beta inhibit epithelial morphogenesis through dysregulation of SOCS-3. Proc Natl Acad Sci USA 2007; 104: 20386-20391.
    • (2007) Proc Natl Acad Sci USA , vol.104 , pp. 20386-20391
    • Ma, Z.1    Gong, Y.2    Patel, V.3
  • 12
    • 0031453186 scopus 로고    scopus 로고
    • Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY
    • Horikawa Y, Iwasaki N, Hara M et al. Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY. Nat Genet 1997; 17: 384-385.
    • (1997) Nat Genet , vol.17 , pp. 384-385
    • Horikawa, Y.1    Iwasaki, N.2    Hara, M.3
  • 13
    • 30944440898 scopus 로고    scopus 로고
    • Roles of HNF-1beta in kidney development and congenital cystic diseases
    • Igarashi P, Shao X, McNally BT et al. Roles of HNF-1beta in kidney development and congenital cystic diseases. Kidney Int 2005; 68: 1944-1947.
    • (2005) Kidney Int , vol.68 , pp. 1944-1947
    • Igarashi, P.1    Shao, X.2    McNally, B.T.3
  • 14
    • 33947237697 scopus 로고    scopus 로고
    • Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys
    • Decramer S, Parant O, Beaufils S et al. Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys. J Am Soc Nephrol 2007; 18: 923-933.
    • (2007) J Am Soc Nephrol , vol.18 , pp. 923-933
    • Decramer, S.1    Parant, O.2    Beaufils, S.3
  • 15
    • 33645454942 scopus 로고    scopus 로고
    • Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort
    • Ulinski T, Lescure S, Beaufils S et al. Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort. J Am Soc Nephrol 2006; 17: 497-503.
    • (2006) J Am Soc Nephrol , vol.17 , pp. 497-503
    • Ulinski, T.1    Lescure, S.2    Beaufils, S.3
  • 16
    • 35348827304 scopus 로고    scopus 로고
    • Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy
    • Mefford HC, Clauin S, Sharp AJ et al. Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy. Am J Hum Genet 2007; 81: 1057-1069.
    • (2007) Am J Hum Genet , vol.81 , pp. 1057-1069
    • Mefford, H.C.1    Clauin, S.2    Sharp, A.J.3
  • 17
    • 0037133954 scopus 로고    scopus 로고
    • PKD1 induces p21(waf1) and regulation of the cell cycle via direct activation of the JAK-STAT signaling pathway in a process requiring PKD2
    • Bhunia AK, Piontek K, Boletta A et al. PKD1 induces p21(waf1) and regulation of the cell cycle via direct activation of the JAK-STAT signaling pathway in a process requiring PKD2. Cell 2002; 109: 157-168.
    • (2002) Cell , vol.109 , pp. 157-168
    • Bhunia, A.K.1    Piontek, K.2    Boletta, A.3
  • 18
    • 0033544962 scopus 로고    scopus 로고
    • Anatomy of a homeoprotein revealed by the analysis of human MODY3 mutations
    • Vaxillaire M, Abderrahmani A, Boutin P et al. Anatomy of a homeoprotein revealed by the analysis of human MODY3 mutations. J Biol Chem 1999; 274: 35639-35646.
    • (1999) J Biol Chem , vol.274 , pp. 35639-35646
    • Vaxillaire, M.1    Abderrahmani, A.2    Boutin, P.3
  • 19
    • 19944407088 scopus 로고    scopus 로고
    • HNF1beta/TCF2 mutations impair transactivation potential through altered co-regulator recruitment
    • Barbacci E, Chalkiadaki A, Masdeu C et al. HNF1beta/TCF2 mutations impair transactivation potential through altered co-regulator recruitment. Hum Mol Genet 2004; 13: 3139-3149.
    • (2004) Hum Mol Genet , vol.13 , pp. 3139-3149
    • Barbacci, E.1    Chalkiadaki, A.2    Masdeu, C.3
  • 20
    • 0035901512 scopus 로고    scopus 로고
    • Transcription factor-dependent regulation of CBP and P/CAF histone acetyltransferase activity
    • Soutoglou E, Viollet B, Vaxillaire M et al. Transcription factor-dependent regulation of CBP and P/CAF histone acetyltransferase activity. EMBO J 2001; 20: 1984-1992.
    • (2001) EMBO J , vol.20 , pp. 1984-1992
    • Soutoglou, E.1    Viollet, B.2    Vaxillaire, M.3
  • 21
    • 46249122875 scopus 로고    scopus 로고
    • Transcription factor HNF1β and novel partners affect nephrogenesis
    • Dudziak K, Mottalebi N, Senkel S et al. Transcription factor HNF1β and novel partners affect nephrogenesis. Kidney Int 2008; 74: 210-217.
    • (2008) Kidney Int , vol.74 , pp. 210-217
    • Dudziak, K.1    Mottalebi, N.2    Senkel, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.