Cargando…

Aberrant splicing in maize rough endosperm3 reveals a conserved role for U12 splicing in eukaryotic multicellular development

RNA splicing of U12-type introns functions in human cell differentiation, but it is not known whether this class of introns has a similar role in plants. The maize ROUGH ENDOSPERM3 (RGH3) protein is orthologous to the human splicing factor, ZRSR2. ZRSR2 mutations are associated with myelodysplastic...

Descripción completa

Detalles Bibliográficos
Autores principales: Gault, Christine M., Martin, Federico, Mei, Wenbin, Bai, Fang, Black, Joseph B., Barbazuk, W. Brad, Settles, A. Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358371/
https://www.ncbi.nlm.nih.gov/pubmed/28242684
http://dx.doi.org/10.1073/pnas.1616173114
_version_ 1782516220259467264
author Gault, Christine M.
Martin, Federico
Mei, Wenbin
Bai, Fang
Black, Joseph B.
Barbazuk, W. Brad
Settles, A. Mark
author_facet Gault, Christine M.
Martin, Federico
Mei, Wenbin
Bai, Fang
Black, Joseph B.
Barbazuk, W. Brad
Settles, A. Mark
author_sort Gault, Christine M.
collection PubMed
description RNA splicing of U12-type introns functions in human cell differentiation, but it is not known whether this class of introns has a similar role in plants. The maize ROUGH ENDOSPERM3 (RGH3) protein is orthologous to the human splicing factor, ZRSR2. ZRSR2 mutations are associated with myelodysplastic syndrome (MDS) and cause U12 splicing defects. Maize rgh3 mutants have aberrant endosperm cell differentiation and proliferation. We found that most U12-type introns are retained or misspliced in rgh3. Genes affected in rgh3 and ZRSR2 mutants identify cell cycle and protein glycosylation as common pathways disrupted. Transcripts with retained U12-type introns can be found in polysomes, suggesting that splicing efficiency can alter protein isoforms. The rgh3 mutant protein disrupts colocalization with a known ZRSR2-interacting protein, U2AF2. These results indicate conserved function for RGH3/ZRSR2 in U12 splicing and a deeply conserved role for the minor spliceosome to promote cell differentiation from stem cells to terminal fates.
format Online
Article
Text
id pubmed-5358371
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-53583712017-03-24 Aberrant splicing in maize rough endosperm3 reveals a conserved role for U12 splicing in eukaryotic multicellular development Gault, Christine M. Martin, Federico Mei, Wenbin Bai, Fang Black, Joseph B. Barbazuk, W. Brad Settles, A. Mark Proc Natl Acad Sci U S A PNAS Plus RNA splicing of U12-type introns functions in human cell differentiation, but it is not known whether this class of introns has a similar role in plants. The maize ROUGH ENDOSPERM3 (RGH3) protein is orthologous to the human splicing factor, ZRSR2. ZRSR2 mutations are associated with myelodysplastic syndrome (MDS) and cause U12 splicing defects. Maize rgh3 mutants have aberrant endosperm cell differentiation and proliferation. We found that most U12-type introns are retained or misspliced in rgh3. Genes affected in rgh3 and ZRSR2 mutants identify cell cycle and protein glycosylation as common pathways disrupted. Transcripts with retained U12-type introns can be found in polysomes, suggesting that splicing efficiency can alter protein isoforms. The rgh3 mutant protein disrupts colocalization with a known ZRSR2-interacting protein, U2AF2. These results indicate conserved function for RGH3/ZRSR2 in U12 splicing and a deeply conserved role for the minor spliceosome to promote cell differentiation from stem cells to terminal fates. National Academy of Sciences 2017-03-14 2017-02-27 /pmc/articles/PMC5358371/ /pubmed/28242684 http://dx.doi.org/10.1073/pnas.1616173114 Text en Freely available online through the PNAS open access option.
spellingShingle PNAS Plus
Gault, Christine M.
Martin, Federico
Mei, Wenbin
Bai, Fang
Black, Joseph B.
Barbazuk, W. Brad
Settles, A. Mark
Aberrant splicing in maize rough endosperm3 reveals a conserved role for U12 splicing in eukaryotic multicellular development
title Aberrant splicing in maize rough endosperm3 reveals a conserved role for U12 splicing in eukaryotic multicellular development
title_full Aberrant splicing in maize rough endosperm3 reveals a conserved role for U12 splicing in eukaryotic multicellular development
title_fullStr Aberrant splicing in maize rough endosperm3 reveals a conserved role for U12 splicing in eukaryotic multicellular development
title_full_unstemmed Aberrant splicing in maize rough endosperm3 reveals a conserved role for U12 splicing in eukaryotic multicellular development
title_short Aberrant splicing in maize rough endosperm3 reveals a conserved role for U12 splicing in eukaryotic multicellular development
title_sort aberrant splicing in maize rough endosperm3 reveals a conserved role for u12 splicing in eukaryotic multicellular development
topic PNAS Plus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358371/
https://www.ncbi.nlm.nih.gov/pubmed/28242684
http://dx.doi.org/10.1073/pnas.1616173114
work_keys_str_mv AT gaultchristinem aberrantsplicinginmaizeroughendosperm3revealsaconservedroleforu12splicingineukaryoticmulticellulardevelopment
AT martinfederico aberrantsplicinginmaizeroughendosperm3revealsaconservedroleforu12splicingineukaryoticmulticellulardevelopment
AT meiwenbin aberrantsplicinginmaizeroughendosperm3revealsaconservedroleforu12splicingineukaryoticmulticellulardevelopment
AT baifang aberrantsplicinginmaizeroughendosperm3revealsaconservedroleforu12splicingineukaryoticmulticellulardevelopment
AT blackjosephb aberrantsplicinginmaizeroughendosperm3revealsaconservedroleforu12splicingineukaryoticmulticellulardevelopment
AT barbazukwbrad aberrantsplicinginmaizeroughendosperm3revealsaconservedroleforu12splicingineukaryoticmulticellulardevelopment
AT settlesamark aberrantsplicinginmaizeroughendosperm3revealsaconservedroleforu12splicingineukaryoticmulticellulardevelopment