Hepatocyte nuclear factor 4α enhances the hepatocyte nuclear factor 1α-mediated activation of transcription

被引:56
作者
Eeckhoute, J [1 ]
Formstecher, P [1 ]
Laine, B [1 ]
机构
[1] Fac Med H Warembourg, Biol Cellulaire Lab, INSERM, U459, F-59045 Lille, France
关键词
D O I
10.1093/nar/gkh581
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatocyte Nuclear Factor 1alpha (HNF1alpha) and Hepatocyte Nuclear Factor 4alpha (HNF4alpha) are two liver-enriched transcription factors coexpressed in specific tissues where they play a crucial role through their involvement in a complex cross-regulatory network. HNF1alpha down regulates HNF4alpha-mediated activation of transcription via a direct protein-protein interaction. Here we show that HNF4alpha enhances the transcriptional activity of HNF1alpha in a DNA binding independent manner, thus indicating that it behaves as a HNF1alpha coactivator. Using mutations in the ligand binding domain (LBD) of HNF4alpha, we confirmed the involvement of the Activation Function 2 module and demonstrated the requirement of the integrity of the LBD for the interaction with HNF1alpha. Moreover, we show that HNF4alpha cooperates with p300 to achieve the highest HNF1alpha-mediated transcription rates. Our findings highlight a new way by which HNF4alpha can regulate gene expression and extend our knowledge of the complexity of the transcriptional network involving HNF4alpha and HNF1alpha.
引用
收藏
页码:2586 / 2593
页数:8
相关论文
共 43 条
  • [1] Hepatocyte nuclear factor-1α recruits the transcriptional co-activator p300 on the GLUT2 gene promoter
    Ban, N
    Yamada, Y
    Someya, Y
    Miyawaki, K
    Ihara, Y
    Hosokawa, M
    Toyokuni, S
    Tsuda, K
    Seino, Y
    [J]. DIABETES, 2002, 51 (05) : 1409 - 1418
  • [2] DEVELOPMENTAL REGULATION AND TISSUE DISTRIBUTION OF THE LIVER TRANSCRIPTION FACTOR LFB1 (HNF1) IN XENOPUS-LAEVIS
    BARTKOWSKI, S
    ZAPP, D
    WEBER, H
    EBERLE, G
    ZOIDL, C
    SENKEL, S
    KLEINHITPASS, L
    RYFFEL, GU
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (01) : 421 - 431
  • [3] Analysis of protein dimerization and ligand binding of orphan receptor HNF4α
    Bogan, AA
    Dallas-Yang, Q
    Ruse, MD
    Maeda, Y
    Jiang, GQ
    Nepomuceno, L
    Scanlan, TS
    Cohen, FE
    Sladek, FM
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2000, 302 (04) : 831 - 851
  • [4] Liver-enriched transcription factors and hepatocyte differentiation
    Cereghini, S
    [J]. FASEB JOURNAL, 1996, 10 (02) : 267 - 282
  • [5] PROPERTIES OF INITIATOR-ASSOCIATED TRANSCRIPTION MEDIATED BY GAL4-VP16
    CHANG, CB
    GRALLA, JD
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (12) : 7469 - 7475
  • [6] COGNET M, 1991, J BIOL CHEM, V266, P7368
  • [7] Crystal structure of the HNF4α ligand binding domain in complex with endogenous fatty acid ligand
    Dhe-Paganon, S
    Duda, K
    Iwamoto, M
    Chi, YI
    Shoelson, SE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (41) : 37973 - 37976
  • [8] Regulation of a transcription factor network required for differentiation and metabolism
    Duncan, SA
    Navas, MA
    Dufort, D
    Rossant, J
    Stoffel, M
    [J]. SCIENCE, 1998, 281 (5377) : 692 - 695
  • [9] Critical role of charged residues in helix 7 of the ligand binding domain in Hepatocyte Nuclear Factor 4α dimerisation and transcriptional activity
    Eeckhoute, J
    Oxombre, B
    Formstecher, P
    Lefebvre, P
    Laine, B
    [J]. NUCLEIC ACIDS RESEARCH, 2003, 31 (22) : 6640 - 6650
  • [10] Hepatocyte nuclear factor 4α Isoforms originated from the P1 promoter are expressed in human pancreatic β-cells and exhibit stronger transcriptional potentials than P2 promoter-driven isoforms
    Eeckhoute, J
    Moerman, E
    Bouckenooghe, T
    Lukoviak, B
    Pattou, F
    Formstecher, P
    Kerr-Conte, J
    Vandewalle, B
    Laine, B
    [J]. ENDOCRINOLOGY, 2003, 144 (05) : 1686 - 1694