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A disease-linked lncRNA mutation in RNase MRP inhibits ribosome synthesis

A disease-linked lncRNA mutation in RNase MRP inhibits ribosome synthesis

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_6d72bec339554c86a887521d12ef03cb

A disease-linked lncRNA mutation in RNase MRP inhibits ribosome synthesis

About this item

Full title

A disease-linked lncRNA mutation in RNase MRP inhibits ribosome synthesis

Publisher

London: Nature Publishing Group UK

Journal title

Nature communications, 2022-02, Vol.13 (1), p.649-14, Article 649

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

RMRP
encodes a non-coding RNA forming the core of the RNase MRP ribonucleoprotein complex. Mutations cause Cartilage Hair Hypoplasia (CHH), characterized by skeletal abnormalities and impaired T cell activation. Yeast RNase MRP cleaves a specific site in the pre-ribosomal RNA (pre-rRNA) during ribosome synthesis. CRISPR-mediated disruption of

Alternative Titles

Full title

A disease-linked lncRNA mutation in RNase MRP inhibits ribosome synthesis

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_6d72bec339554c86a887521d12ef03cb

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_6d72bec339554c86a887521d12ef03cb

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/s41467-022-28295-8

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