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Ribosomal RNA 2′-O-methylation dynamics impact cell fate decisions

Häfner, Sophia J. (author)
University of Copenhagen
Jansson, Martin D. (author)
University of Copenhagen
Altinel, Kübra (author)
University of Copenhagen
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Andersen, Kasper L. (author)
University of Copenhagen
Abay-Nørgaard, Zehra (author)
University of Copenhagen
Ménard, Patrice (author)
University of Copenhagen
Fontenas, Martin (author)
University of Copenhagen
Sørensen, Daniel M. (author)
University of Copenhagen
Gay, David M. (author)
University of Copenhagen
Arendrup, Frederic S. (author)
University of Copenhagen
Tehler, Disa (author)
University of Copenhagen
Krogh, Nicolai (author)
University of Copenhagen
Nielsen, Henrik (author)
University of Copenhagen
Kraushar, Matthew L. (author)
Max Planck Institute for Molecular Genetics
Kirkeby, Agnete (author)
Lund University,Lunds universitet,Human neural utvecklingsbiologi,Forskargrupper vid Lunds universitet,WCMM- Wallenberg center för molekylär medicinsk forskning,Medicinska fakulteten,Human Neural Developmental Biology,Lund University Research Groups,WCMM-Wallenberg Centre for Molecular Medicine,Faculty of Medicine,University of Copenhagen
Lund, Anders H. (author)
University of Copenhagen
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 (creator_code:org_t)
2023
2023
English.
In: Developmental Cell. - 1534-5807. ; 58:17, s. 9-1609
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Translational regulation impacts both pluripotency maintenance and cell differentiation. To what degree the ribosome exerts control over this process remains unanswered. Accumulating evidence has demonstrated heterogeneity in ribosome composition in various organisms. 2′-O-methylation (2′-O-me) of rRNA represents an important source of heterogeneity, where site-specific alteration of methylation levels can modulate translation. Here, we examine changes in rRNA 2′-O-me during mouse brain development and tri-lineage differentiation of human embryonic stem cells (hESCs). We find distinct alterations between brain regions, as well as clear dynamics during cortex development and germ layer differentiation. We identify a methylation site impacting neuronal differentiation. Modulation of its methylation levels affects ribosome association of the fragile X mental retardation protein (FMRP) and is accompanied by an altered translation of WNT pathway-related mRNAs. Together, these data identify ribosome heterogeneity through rRNA 2′-O-me during early development and differentiation and suggest a direct role for ribosomes in regulating translation during cell fate acquisition.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Keyword

2′-O-methylation
brain development
cell fate
development
differentiation
human embryonic stem cells
neurogenesis
ribosome
RNA modifications
translation
translation programs

Publication and Content Type

art (subject category)
ref (subject category)

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