Alternative splicing in multiple sclerosis and other autoimmune diseases.

dc.contributor.author

Evsyukova, Irina

dc.contributor.author

Somarelli, Jason A

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Gregory, Simon G

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Garcia-Blanco, Mariano A

dc.coverage.spatial

United States

dc.date.accessioned

2011-06-21T17:21:59Z

dc.date.issued

2010-07

dc.description.abstract

Alternative splicing is a general mechanism for regulating gene expression that affects the RNA products of more than 90% of human genes. Not surprisingly, alternative splicing is observed among gene products of metazoan immune systems, which have evolved to efficiently recognize pathogens and discriminate between "self" and "non-self", and thus need to be both diverse and flexible. In this review we focus on the specific interface between alternative splicing and autoimmune diseases, which result from a malfunctioning of the immune system and are characterized by the inappropriate reaction to self-antigens. Despite the widespread recognition of alternative splicing as one of the major regulators of gene expression, the connections between alternative splicing and autoimmunity have not been apparent. We summarize recent findings connecting splicing and autoimmune disease, and attempt to find common patterns of splicing regulation that may advance our understanding of autoimmune diseases and open new avenues for therapy.

dc.description.version

Version of Record

dc.identifier

http://www.ncbi.nlm.nih.gov/pubmed/20639696

dc.identifier

12301

dc.identifier.eissn

1555-8584

dc.identifier.uri

https://hdl.handle.net/10161/3963

dc.language

eng

dc.language.iso

en_US

dc.publisher

Informa UK Limited

dc.relation.ispartof

RNA Biol

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Rna Biology

dc.subject

Alternative Splicing

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Animals

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Autoimmune Diseases

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Exons

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Humans

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Multiple Sclerosis

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Receptors, Interleukin-7

dc.title

Alternative splicing in multiple sclerosis and other autoimmune diseases.

dc.title.alternative
dc.type

Journal article

duke.contributor.orcid

Somarelli, Jason A|0000-0003-1510-9343

duke.contributor.orcid

Gregory, Simon G|0000-0002-7805-1743

duke.date.pubdate

2010-8-jul

duke.description.issue

4

duke.description.volume

7

pubs.author-url

http://www.ncbi.nlm.nih.gov/pubmed/20639696

pubs.begin-page

462

pubs.end-page

473

pubs.issue

4

pubs.organisational-group

Basic Science Departments

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Clinical Science Departments

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Duke

pubs.organisational-group

Duke Cancer Institute

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Duke Molecular Physiology Institute

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Institutes and Centers

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Molecular Genetics and Microbiology

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Neurology

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Neurology, MS & Neuroimmunology

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School of Medicine

pubs.publication-status

Published

pubs.volume

7

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