Evidence map›Paper›PMID 41593673›Full record

ArticleGenome biology2026

Circularization of 23S rRNA but not 16S rRNA within archaeal ribosomes.

Ling-Dong Shi, Petar I Penev, Amos J Nissley, Dipti D Nayak, Rohan Sachdeva, Jamie H D Cate, Jillian F Banfield

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Article in Genome biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Archaeal RNA processing and regulation: expanding the functional landscape.Microbiology and molecular biology reviews : MMBR · 2025
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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Ling-Dong ShiInnovative Genomics Institute, University of California, Berkeley, CA, USA. lingdong_shi@berkeley.edu.
Petar I PenevInnovative Genomics Institute, University of California, Berkeley, CA, USA.
Amos J NissleyDepartment of Chemistry, University of California, Berkeley, CA, USA.
Dipti D NayakDepartment of Molecular and Cell Biology, University of California, Berkeley, CA, USA.
Rohan SachdevaInnovative Genomics Institute, University of California, Berkeley, CA, USA.
Jamie H D CateInnovative Genomics Institute, University of California, Berkeley, CA, USA.
Jillian F BanfieldInnovative Genomics Institute, University of California, Berkeley, CA, USA. jbanfield@berkeley.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProcessing of archaeal 16S and 23S rRNAs is believed to involve excision of individual rRNAs from polycistronic precursors, circularization of excised rRNAs, and re-linearization before the incorporation into ribosomes. However, all the knowledge is derived from several isolated species, leaving open the possibility that different processes may occur in other archaeal groups.

resultsHere, we investigate rRNAs from diverse and mostly uncultivated archaea. Sequencing of total cellular RNA from eight phylum-level lineages indicates that archaeal circular 23S rRNA transcript abundances vastly exceed those of linear counterparts, and linear versions are often undetectable. As the majority of rRNAs derive from mature ribosomes, the data suggest that ribosomes contain circular 23S rRNAs. Thus, we directly sequence RNA extracted from isolated ribosomes of a model archaeon, Methanosarcina acetivorans, and confirm that the 23S rRNAs in the ribosomes are circular. Structural modeling places the 5' and 3' ends of the linear precursors of archaeal 23S rRNAs in close proximity to form a GNRA tetraloop (in which N is A, C, G, or U and R is A or G), consistent with their existence as circular molecules. We also confirm the existence of circular 16S rRNA intermediates in transcriptomes of most archaea, yet a circular form is not evident in some distinct archaeal groups, suggesting that certain archaea do not circularize 16S rRNA during processing.

conclusionsOur findings uncover unexpected variations in the processing required to generate mature rRNAs and the conformation of functional molecules in archaeal ribosomes.

Indexed as

ArchaeaRibosomesRNA, ArchaealRNA, Ribosomal, 16SRNA, Ribosomal, 23SNucleic Acid ConformationRNA, ArchaealRNA, Ribosomal, 16SRNA, Ribosomal, 23SArchaeaCircular 23S rRNAMetatranscriptomicsMethanosarcinarRNA processing

Identifiers

PMID41593673
PMCPMC12918454

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.