MBNL1 associates with YB-1 in cytoplasmic stress granules (Q24310407)

GOA release 2020-03-11

DEAD-box helicase 1

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GOA release 2020-03-11

Y-box binding protein 1

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GOA release 2020-03-11

author name string

Hayato Onishi

1

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Yoshihiro Kino

2

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Tomoko Morita

3

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Eugene Futai

4

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Noboru Sasagawa

5

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Shoichi Ishiura

Journal of Neuroscience Research

6

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language of work or name

English

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publication date

July 2008

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published in

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volume

86

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issue

9

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page(s)

1994-2002

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cites work

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Expression and polysome association of YB-1 in various tissues at different stages in the lifespan of mice.

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The pleiotropic functions of the Y-box-binding protein, YB-1.

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The muscleblind gene participates in the organization of Z-bands and epidermal attachments of Drosophila muscles and is regulated by Dmef2.

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The DEAD-box protein family of RNA helicases

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RNA splicing mediated by YB-1 is inhibited by TLS/CHOP in human myxoid liposarcoma cells

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Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2).

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The Microprocessor complex mediates the genesis of microRNAs

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RNA-dependent integrin alpha3 protein localization regulated by the Muscleblind-like protein MLP1

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Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.

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Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy

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Alternative splicing regulation by interaction of phosphatase PP2Cgamma with nucleic acid-binding protein YB-1

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Muscleblind proteins regulate alternative splicing

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Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.

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Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy

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Cell stress modulates the function of splicing regulatory protein RBM4 in translation control

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Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts

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Physical and functional interaction between two pluripotent proteins, the Y-box DNA/RNA-binding factor, YB-1, and the multivalent zinc finger factor, CTCF

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Splicing factor SRp30c interaction with Y-box protein-1 confers nuclear YB-1 shuttling and alternative splice site selection

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Mammalian Smaug is a translational repressor that forms cytoplasmic foci similar to stress granules

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A novel Ded1-like RNA helicase interacts with the Y-box protein ctYB-1 in nuclear mRNP particles and in polysomes.

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Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues

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Evidence that ternary complex (eIF2-GTP-tRNA(i)(Met))-deficient preinitiation complexes are core constituents of mammalian stress granules

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Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy

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The RNA binding protein YB-1 binds A/C-rich exon enhancers and stimulates splicing of the CD44 alternative exon v4.

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Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2.

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Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells.

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Cis and trans effects of the myotonic dystrophy (DM) mutation in a cell culture model

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Muscleblind protein, MBNL1/EXP, binds specifically to CHHG repeats

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Myotonic dystrophy associated expanded CUG repeat muscleblind positive ribonuclear foci are not toxic to Drosophila.

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In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts

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The Muscleblind family of proteins: an emerging class of regulators of developmentally programmed alternative splicing

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Muscleblind isoforms are functionally distinct and regulate alpha-actinin splicing.

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Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

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Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

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Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat

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Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.

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LINE-1 ORF1 protein localizes in stress granules with other RNA-binding proteins, including components of RNA interference RNA-induced silencing complex

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DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model

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Probing the mRNA processing body using protein macroarrays and "autoantigenomics".

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Differential regulation of the serotonin transporter gene by lithium is mediated by transcription factors, CCCTC binding protein and Y-box binding protein 1, through the polymorphic intron 2 variable number tandem repeat

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YB-1 and CTCF differentially regulate the 5-HTT polymorphic intron 2 enhancer which predisposes to a variety of neurological disorders

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7 January 2021

Fragile X mental retardation protein shifts between polyribosomes and stress granules after neuronal injury by arsenite stress or in vivo hippocampal electrode insertion

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7 January 2021

Identifiers

DOI

10.1002/JNR.21655

1 reference

Consolidated OpenCitations Corpus – April 2017

4732724

4732724

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference