Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation function.
about
Emerin caps the pointed end of actin filaments: evidence for an actin cortical network at the nuclear inner membraneThe vaccinia-related kinases phosphorylate the N' terminus of BAF, regulating its interaction with DNA and its retention in the nucleusZinc-finger domains of the transcriptional repressor KLF15 bind multiple sites in rhodopsin and IRBP promoters including the CRS-1 and G-rich repressor elementsBarrier-to-autointegration factor BAF binds p55 Gag and matrix and is a host component of human immunodeficiency virus type 1 virionsMultiple roles for emerin: implications for Emery-Dreifuss muscular dystrophyBarrier to Autointegration Factor (BANF1): interwoven roles in nuclear structure, genome integrity, innate immunity, stress responses and progeriaTranscriptional repressor germ cell-less (GCL) and barrier to autointegration factor (BAF) compete for binding to emerin in vitroThe nuclear envelope at a glanceThe photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genesBarrier to autointegration factor blocks premature cell fusion and maintains adult muscle integrity in C. elegans.Barrier-to-autointegration factor proteome reveals chromatin-regulatory partners.Kruppel-like factor 15, a zinc-finger transcriptional regulator, represses the rhodopsin and interphotoreceptor retinoid-binding protein promotersAn emerin "proteome": purification of distinct emerin-containing complexes from HeLa cells suggests molecular basis for diverse roles including gene regulation, mRNA splicing, signaling, mechanosensing, and nuclear architecture.FIZ1 is part of the regulatory protein complex on active photoreceptor-specific gene promoters in vivo.Genome-wide analysis links emerin to neuromuscular junction activity in Caenorhabditis elegans.Nuclear envelope and lamin B2 function in the central nervous system.Barrier-to-autointegration factor is required to segregate and enclose chromosomes within the nuclear envelope and assemble the nuclear laminaMutation discovered in a feline model of human congenital retinal blinding disease.No interaction of barrier-to-autointegration factor (BAF) with HIV-1 MA, cone-rod homeobox (Crx) or MAN1-C in absence of DNASystems analysis of the prostate tumor suppressor NKX3.1 supports roles in DNA repair and luminal cell differentiation.New role for EMD (emerin), a key inner nuclear membrane protein, as an enhancer of autophagosome formation in the C16-ceramide autophagy pathwayDirect binding of nuclear membrane protein MAN1 to emerin in vitro and two modes of binding to barrier-to-autointegration factor.Barrier-to-autointegration factor phosphorylation on Ser-4 regulates emerin binding to lamin A in vitro and emerin localization in vivo.Lmo7 is an emerin-binding protein that regulates the transcription of emerin and many other muscle-relevant genes.Nucleoplasmic lamins and their interaction partners, LAP2alpha, Rb, and BAF, in transcriptional regulation.Mouse retinal development: a dark horse model for systems biology researchMechanistically distinct mouse models for CRX-associated retinopathy.Barrier to auto integration factor becomes dephosphorylated during HSV-1 Infection and Can Act as a host defense by impairing viral DNA replication and gene expressionEmerin in health and disease.Néstor-Guillermo Progeria Syndrome: a biochemical insight into Barrier-to-Autointegration Factor 1, alanine 12 threonine mutationMolecular characterization of the host defense activity of the barrier to autointegration factor against vaccinia virus.Barrier-to-Autointegration Factor 1 (BAF/BANF1) Promotes Association of the SETD1A Histone Methyltransferase with Herpes Simplex Virus Immediate-Early Gene Promoters.Nuclear lamins: key regulators of nuclear structure and activitiesBarrier-to-Autointegration Factor influences specific histone modificationsEarly aberrations in chromatin dynamics in embryos produced under in vitro conditions.Transcriptional factors involved in photoreceptor differentiation.Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution.Crx activates opsin transcription by recruiting HAT-containing co-activators and promoting histone acetylation.Regulation of photoreceptor gene expression by Crx-associated transcription factor networkDepletion of the protein kinase VRK1 disrupts nuclear envelope morphology and leads to BAF retention on mitotic chromosomes
P2860
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P2860
Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation function.
description
2002 nî lūn-bûn
@nan
2002 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Barrier to autointegration fac ...... its transactivation function.
@ast
Barrier to autointegration fac ...... its transactivation function.
@en
type
label
Barrier to autointegration fac ...... its transactivation function.
@ast
Barrier to autointegration fac ...... its transactivation function.
@en
prefLabel
Barrier to autointegration fac ...... its transactivation function.
@ast
Barrier to autointegration fac ...... its transactivation function.
@en
P2093
P2860
P356
P1476
Barrier to autointegration fac ...... its transactivation function.
@en
P2093
Ching-Hwa Sung
Eliot L Berson
Guang-Hua Peng
Prabodh K Swain
Shiming Chen
Thaddeus P Dryja
Xuejiao Wang
P2860
P304
43288-43300
P356
10.1074/JBC.M207952200
P407
P577
2002-09-04T00:00:00Z