4.8 Article

Ribosome heterogeneity in Drosophila melanogaster gonads through paralog-switching

期刊

NUCLEIC ACIDS RESEARCH
卷 50, 期 4, 页码 2240-2257

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OXFORD UNIV PRESS
DOI: 10.1093/nar/gkab606

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资金

  1. Royal Society [RSG\R1\180102]
  2. BBSRC [BB/S007407/1]
  3. Wellcome Trust ISSF [105615/Z/14/Z]
  4. MRC [MR/N000471/1]
  5. BBSRC DTP [BB/M011151/1]
  6. University of Leeds
  7. Wellcome Trust [108466/Z/15/Z]
  8. White Rose University Consortium-Collaborative Grant
  9. Wellcome Trust [105615/Z/14/Z] Funding Source: Wellcome Trust
  10. BBSRC [BB/S007407/1] Funding Source: UKRI
  11. MRC [MR/N000471/1] Funding Source: UKRI

向作者/读者索取更多资源

Research has found heterogeneity in ribosomal protein composition across different tissues of Drosophila melanogaster, particularly in the testes and ovaries, which is achieved through paralog-enrichment and switching. The study also reveals differences in ribosomal arrangement and amino acid composition of paralog pairs between tissues, suggesting that paralog-switching may alter the ribosome surface and enable different proteins to regulate translation.
Ribosomes have long been thought of as homogeneous macromolecular machines, but recent evidence suggests they are heterogeneous and could be specialised to regulate translation. Here, we have characterised ribosomal protein heterogeneity across 4 tissues of Drosophila melanogaster. We find that testes and ovaries contain the most heterogeneous ribosome populations, which occurs through a combination of paralog-enrichment and paralog-switching. We have solved structures of ribosomes purified from in vivo tissues by cryo-EM, revealing differences in precise ribosomal arrangement for testis and ovary 80S ribosomes. Differences in the amino acid composition of paralog pairs and their localisation on the ribosome exterior indicate paralog-switching could alter the ribosome surface, enabling different proteins to regulate translation. One testis-specific paralog-switching pair is also found in humans, suggesting this is a conserved site of ribosome heterogeneity. Overall, this work allows us to propose that mRNA translation might be regulated in the gonads through ribosome heterogeneity, providing a potential means of ribosome specialisation.

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