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Minor intron splicing revisited: identification of new minor intron-containing genes and tissue-dependent retention and alternative splicing of minor introns

BACKGROUND: Mutations in minor spliceosome components such as U12 snRNA (cerebellar ataxia) and U4atac snRNA (microcephalic osteodysplastic primordial dwarfism type 1 (MOPD1)) result in tissue-specific symptoms. Given that the minor spliceosome is ubiquitously expressed, we hypothesized that these r...

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Foilsithe in:BMC Genomics
Main Authors: Olthof, Anouk M., Hyatt, Katery C., Kanadia, Rahul N.
Formáid: Artigo
Teanga:Inglês
Foilsithe: BioMed Central 2019
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6717393/
https://ncbi.nlm.nih.gov/pubmed/31470809
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-019-6046-x
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