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Cell signalling

HSP90 family across kingdoms

Chen B, Zhong D, Monteiro A · BMC genomics · 2006

Open access · cc by · source: Europe PMC

Comparative genomics maps 103 HSP90-family genes across 32 genomes and deep phylogenetic diversity.

Study at a glance

Design
Computational / modelling — Multi-kingdom survey of HSP90 homologs and phylogeny across sequenced genomes
N
N=32 · 32 genomes yielding 103 HSP90-family genes (87 functional, 16 pseudogenes); phylogeny used 197 sequences
Population
Sequenced genomes spanning Archaea, Bacteria, and Eukarya
Outcome
Distribution and evolutionary relationships of the HSP90 gene family

Structured fields used in claim comparison tables when every cited study has a complete layer.

Key findings

103 genes on 32 genomes (87 functional, 16 pseudogenes); vertebrates have the largest counts; Archaea nearly lack HSP90.

Methodology

Surveyed genomes for HSP90 homologs, classified functional genes vs pseudogenes, and built multi-kingdom phylogenies.

Limitations

Does not experimentally mutate each homolog’s chaperone clients.

How this study connects

Role on claims

Each row is a claim on a concept or method page where this paper supports, challenges, or qualifies the statement. Roles are hand-checked — not a model guess.

  • SupportsCell signallingconcept

    103 genes on 32 genomes (87 functional, 16 pseudogenes); vertebrates have the largest counts; Archaea nearly lack HSP90.

    Evidence for the claim as stated.

  • SupportsPhylogenetic Analysismethod

    A multi-kingdom HSP90 survey found 103 genes on 32 genomes (87 functional, 16 pseudogenes). Vertebrates had the largest counts; Archaea nearly lack HSP90. The phylogeny classifies homologs and pseudogenes; it does not mutate each homolog's chaperone clients.

    Evidence for the claim as stated.

  • SupportsPhylogenetic Analysismethod

    These papers do not build the same kind of tree. HSP90 and MYB papers classify gene families; the immune-gene paper scans orthologs for repeated positive selection (~14% selected in all tests); Aspergillus and Listeria papers mix clade phylogeny with pan-genome gene content; turtle and Medicago papers are organismal genomes whose phylogeny is background for physiology or breeding. A student who treats every 'phylogenetic analysis' hit as a species tree will misread the result.

    Evidence for the claim as stated.

Open questions

Tensions this paper is part of

From concept pages' “where studies disagree.” Disagreement means the same question; scope means different assays, populations, or outcomes.

  • Scope difference — different assays, populations, or outcomes

    These papers do not build the same kind of tree. HSP90 and MYB papers classify gene families; the immune-gene paper scans orthologs for repeated positive selection (~14% selected in all tests); Aspergillus and Listeria papers mix clade phylogeny with pan-genome gene content; turtle and Medicago papers are organismal genomes whose phylogeny is background for physiology or breeding. A student who treats every 'phylogenetic analysis' hit as a species tree will misread the result.

Related papers in this topic

Same topic cluster — not a recommendation engine.