Myotonic dystrophy protein kinase is critical for nuclear envelope integrity (Q24338683)

Dystrophia myotonica-protein kinase

GOA release 2020-03-11

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GOA release 2020-03-11

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Erin B Harmon

1

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Michelle L Harmon

2

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Tricia D Larsen

3

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Jie Yang

4

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Joseph W Glasford

5

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M Benjamin Perryman

Journal of Biological Chemistry

6

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language of work or name

English

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publication date

18 November 2011

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published in

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volume

286

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page(s)

40296-306

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issue

46

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cites work

Myotonic dystrophy protein kinase is expressed in embryonic myocytes and is required for myotube formation

1 reference

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Myotonic dystrophy protein kinase phosphorylates phospholamban and regulates calcium uptake in cardiomyocyte sarcoplasmic reticulum

19 March 2017

1 reference

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Emerin binding to Btf, a death-promoting transcriptional repressor, is disrupted by a missense mutation that causes Emery-Dreifuss muscular dystrophy

19 March 2017

1 reference

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In vivo and in vitro interaction between human transcription factor MOK2 and nuclear lamin A/C.

19 March 2017

1 reference

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Myotonic dystrophy protein kinase domains mediate localization, oligomerization, novel catalytic activity, and autoinhibition

19 March 2017

1 reference

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Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy

19 March 2017

1 reference

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Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C

19 March 2017

1 reference

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Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum

19 March 2017

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Transcriptional repressor germ cell-less (GCL) and barrier to autointegration factor (BAF) compete for binding to emerin in vitro

19 March 2017

1 reference

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A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies

19 March 2017

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Distinct changes in intranuclear lamin A/C organization during myoblast differentiation

19 March 2017

1 reference

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

19 March 2017

1 reference

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RNA CUG repeats sequester CUGBP1 and alter protein levels and activity of CUGBP1

19 March 2017

1 reference

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

19 March 2017

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A muscleblind knockout model for myotonic dystrophy

19 March 2017

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Emerin and the nuclear lamina in muscle and cardiac disease.

19 March 2017

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Nuclear lamins: major factors in the structural organization and function of the nucleus and chromatin

27 September 2017

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Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

RNA toxicity in myotonic muscular dystrophy induces NKX2-5 expression

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Nuclear envelope defects in muscular dystrophy.

27 September 2017

1 reference

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Myotonic dystrophy: emerging mechanisms for DM1 and DM2.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Transgenic mice expressing CUG-BP1 reproduce splicing mis-regulation observed in myotonic dystrophy.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Sequestration of pRb by cyclin D3 causes intranuclear reorganization of lamin A/C during muscle cell differentiation.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

The nuclear envelope and human disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Transgenic mouse models for myotonic dystrophy type 1 (DM1)

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Changes in myotonic dystrophy protein kinase levels and muscle development in congenital myotonic dystrophy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Myotonic dystrophy protein kinase monoclonal antibody generation from a coiled-coil template

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Loss of emerin at the nuclear envelope disrupts the Rb1/E2F and MyoD pathways during muscle regeneration.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Overexpression of Human Myotonic Dystrophy Protein Kinase in Schizosaccharomyces pombe Induces an Abnormal Polarized and Swollen Cell Morphology

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

The nuclear lamin protein family in higher vertebrates. Identification of quantitatively minor lamin proteins by monoclonal antibodies.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220565

Overexpression of CUG triplet repeat-binding protein, CUGBP1, in mice inhibits myogenesis.

30 May 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.241455

Remodelling of the nuclear lamina and nucleoskeleton is required for skeletal muscle differentiation in vitro.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.241455

Insect lipoprotein follows a transferrin-like recycling pathway that is mediated by the insect LDL receptor homologue

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.241455

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.241455

Decreased mechanical stiffness in LMNA-/- cells is caused by defective nucleo-cytoskeletal integrity: implications for the development of laminopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.241455

Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblasts

21 January 2018

1 reference

12 December 2020

Complex formation between lamin A and the retinoblastoma gene product: identification of the domain on lamin A required for its interaction

1 reference

12 December 2020

Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation

1 reference

12 December 2020

Effect of Myotonic Dystrophy Trinucleotide Repeat Expansion on DMPK Transcription and Processing

1 reference

12 December 2020