Evidence map›Paper›PMID 39169013›Full record

ArticleNature communications2024

Altered assembly paths mitigate interference among paralogous complexes.

Chi-Wei Yeh, Kuan-Lun Hsu, Shu-Ting Lin, Wei-Chieh Huang, Kun-Hai Yeh, Chien-Fu Jeff Liu, Li-Chin Wang, Ting-Ting Li, Shu-Chuan Chen, Chen-Hsin Yu and 3 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
4 · The record

Corrections and comments

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

13 authors.

Chi-Wei YehInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Kuan-Lun HsuInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.ORCID 0000-0002-4131-1775
Shu-Ting LinInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Wei-Chieh HuangInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Kun-Hai YehInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Chien-Fu Jeff LiuInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Li-Chin WangInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Ting-Ting LiInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Shu-Chuan ChenInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Chen-Hsin YuInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.ORCID 0000-0002-5662-3026
Jun-Yi LeuInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Chen-Hsiang YeangGenome and Systems Biology Degree Program, National Taiwan University and Academia Sinica, Taipei, Taiwan.
Hsueh-Chi S YenInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan. hyen@imb.sinica.edu.tw.ORCID 0000-0003-3511-4414

Funding

Academia Sinica AS-IA-108-L02; AS-IA-110-L01
6 · The paper itself

Abstract

Protein complexes are fundamental to all cellular processes, so understanding their evolutionary history and assembly processes is important. Gene duplication followed by divergence is considered a primary mechanism for diversifying protein complexes. Nonetheless, to what extent assembly of present-day paralogous complexes has been constrained by their long evolutionary pathways and how cross-complex interference is avoided remain unanswered questions. Subunits of protein complexes are often stabilized upon complex formation, whereas unincorporated subunits are degraded. How such cooperative stability influences protein complex assembly also remains unclear. Here, we demonstrate that subcomplexes determined by cooperative stabilization interactions serve as building blocks for protein complex assembly. We further develop a protein stability-guided method to compare the assembly processes of paralogous complexes in cellulo. Our findings support that oligomeric state and the structural organization of paralogous complexes can be maintained even if their assembly processes are rearranged. Our results indicate that divergent assembly processes by paralogous complexes not only enable the complexes to evolve new functions, but also reinforce their segregation by establishing incompatibility against deleterious hybrid assemblies.

Indexed as

Multiprotein ComplexesEvolution, MolecularGene DuplicationProtein BindingProtein MultimerizationProtein StabilityProtein SubunitsMultiprotein ComplexesProtein Subunits

Identifiers

PMID39169013
PMCPMC11339298

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

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 Socratic graph.