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SREBP-1, A BASIC-HELIX-LOOP-HELIX-LEUCINE ZIPPER PROTEIN THAT CONTROLS TRANSCRIPTION OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE
被引:565
|作者:
YOKOYAMA, C
[1
]
WANG, XD
[1
]
BRIGGS, MR
[1
]
ADMON, A
[1
]
WU, J
[1
]
HUA, XX
[1
]
GOLDSTEIN, JL
[1
]
BROWN, MS
[1
]
机构:
[1] UNIV CALIF BERKELEY,DEPT MOLEC & CELL BIOL,HOWARD HUGHES MED INST,BERKELEY,CA 94720
来源:
关键词:
D O I:
10.1016/S0092-8674(05)80095-9
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:
Sterol regulatory element 1 (SRE-1), a decamer (5'-ATC-ACCCCAC-3') flanking the low density lipoprotein (LDL) receptor gene, activates transcription in sterol-depleted cells and is silenced by sterols. We report the cDNA cloning of human SREBP-1, a protein that binds SRE-1, activates transcription, and thereby mediates the final regulatory step in LDL metabolism. SREBP-1 contains a basic-helix-loop-helix-leucine zipper (bHLH-ZIP) motif, but it differs from other bHLH-ZIP proteins in its larger size (I 147 amino acids) and target sequence. Instead of an inverted repeat (CANNTG), the target for all known bHLH-ZIP proteins, SRE-1 contains a direct repeat of CAC. Overexpression of SREBP-1 activates transcription of reporter genes containing SRE-1 in the absence (15-fold) and presence (90-fold) of sterols, abolishing sterol regulation. We suggest that SREBP-1 is regulated by an unknown factor that is overwhelmed when SREBP-1 is overexpressed. Understanding the regulation of SREBP-1 may be crucial for understanding the control of plasma cholesterol in humans.
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页码:187 / 197
页数:11
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