Interaction of the CCAAT displacement protein with shared regulatory elements required for transcription of paired histone genes.
about
Identification of HiNF-P, a key activator of cell cycle-controlled histone H4 genes at the onset of S phaseHiNF-P directly links the cyclin E/CDK2/p220NPAT pathway to histone H4 gene regulation at the G1/S phase cell cycle transition.Molecular regulation of beta-lactam biosynthesis in filamentous fungiCCAAT displacement protein/cut homolog recruits G9a histone lysine methyltransferase to repress transcriptionRegulation of the homeodomain CCAAT displacement/cut protein function by histone acetyltransferases p300/CREB-binding protein (CBP)-associated factor and CBPPhosphorylation of the CCAAT displacement protein (CDP)/Cux transcription factor by cyclin A-Cdk1 modulates its DNA binding activity in G(2)Smad1 and Smad8 function similarly in mammalian central nervous system development.Genetic ablation of the CDP/Cux protein C terminus results in hair cycle defects and reduced male fertilityRegulation of the pancreatic islet-specific gene BETA2 (neuroD) by neurogenin 3.Identification of a second conserved element within the coding sequence of a mouse H3 histone gene that interacts with nuclear factors and is necessary for normal expressionC/EBP epsilon mediates myeloid differentiation and is regulated by the CCAAT displacement protein (CDP/cut).p110 CUX1 cooperates with E2F transcription factors in the transcriptional activation of cell cycle-regulated genes.Chemotherapy for the brain: the antitumor antibiotic mithramycin prolongs survival in a mouse model of Huntington's disease.CDP/cut is the DNA-binding subunit of histone gene transcription factor HiNF-D: a mechanism for gene regulation at the G1/S phase cell cycle transition point independent of transcription factor E2FCCAAT displacement activity involves CUT repeats 1 and 2, not the CUT homeodomain.YY1 binds five cis-elements and trans-activates the myeloid cell-restricted gp91(phox) promoter.Expression of N-terminally truncated isoforms of CDP/CUX is increased in human uterine leiomyomas.The N-terminal region of the CCAAT displacement protein (CDP)/Cux transcription factor functions as an autoinhibitory domain that modulates DNA binding.A novel colonic repressor element regulates intestinal gene expression by interacting with Cux/CDPIdentification of a major cis-acting DNA element controlling the bidirectionally transcribed penicillin biosynthesis genes acvA (pcbAB) and ipnA (pcbC) of Aspergillus nidulansRegulation of murine Tap1 and Lmp2 genes in macrophages by interferon gamma is mediated by STAT1 and IRF-1.Different requirements for signal transducer and activator of transcription 1alpha and interferon regulatory factor 1 in the regulation of low molecular mass polypeptide 2 and transporter associated with antigen processing 1 gene expression.The CCAAT binding factor can mediate interactions between CONSTANS-like proteins and DNA.
P2860
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P2860
Interaction of the CCAAT displacement protein with shared regulatory elements required for transcription of paired histone genes.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Interaction of the CCAAT displ ...... ption of paired histone genes.
@ast
Interaction of the CCAAT displ ...... ption of paired histone genes.
@en
type
label
Interaction of the CCAAT displ ...... ption of paired histone genes.
@ast
Interaction of the CCAAT displ ...... ption of paired histone genes.
@en
prefLabel
Interaction of the CCAAT displ ...... ption of paired histone genes.
@ast
Interaction of the CCAAT displ ...... ption of paired histone genes.
@en
P2860
P356
P1476
Interaction of the CCAAT displ ...... ption of paired histone genes.
@en
P2093
H M el-Hodiri
P2860
P304
P356
10.1128/MCB.15.7.3587
P407
P577
1995-07-01T00:00:00Z