Evidence map›Paper›PMID 19442299›Full record

ArticleBMC evolutionary biology2009

Phylogeny and evolution of Rab7 and Rab9 proteins.

Paweł Mackiewicz, Elzbieta Wyroba

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 23% of its field
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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Mammalian evolution and human mutation burden in Rab GTPases.Biochemistry and biophysics reports · 2026
    Article
  2. Article
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  5. Choanoflagellates and the ancestry of neurosecretory vesicles.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Article
  6. Article
  7. The Rab7 subfamily acrossSmall GTPases · 2020
    Article
  8. Review
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  10. Article
  11. Article
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  14. Article
  15. Review
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  18. Rab protein evolution and the history of the eukaryotic endomembrane system.Cellular and molecular life sciences : CMLS · 2010
    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

2 authors at 2 institutions in 1 country.

Paweł MackiewiczUniversity of Wrocław, Faculty of Biotechnology, Department of Genomics, 63/77 Przybyszewskiego Street, 51-148 Wrocław, Poland. pamac@smorfland.uni.wroc.pl
Elzbieta Wyroba
Instytut Biologii Doświadczalnej im. Marcelego Nenckiego · PLUniversity of Wrocław · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAn important role in the evolution of intracellular trafficking machinery in eukaryotes played small GTPases belonging to the Rab family known as pivotal regulators of vesicle docking, fusion and transport. The Rab family is very diversified and divided into several specialized subfamilies. We focused on the VII functional group comprising Rab7 and Rab9, two related subfamilies, and analysed 210 sequences of these proteins. Rab7 regulates traffic from early to late endosomes and from late endosome to vacuole/lysosome, whereas Rab9 participates in transport from late endosomes to the trans-Golgi network.

resultsAlthough Rab7 and Rab9 proteins are quite small and show heterogeneous rates of substitution in different lineages, we found a phylogenetic signal and inferred evolutionary relationships between them. Rab7 proteins evolved before radiation of main eukaryotic supergroups while Rab9 GTPases diverged from Rab7 before split of choanoflagellates and metazoans. Additional duplication of Rab9 and Rab7 proteins resulting in several isoforms occurred in the early evolution of vertebrates and next in teleost fishes and tetrapods. Three Rab7 lineages emerged before divergence of monocots and eudicots and subsequent duplications of Rab7 genes occurred in particular angiosperm clades. Interestingly, several Rab7 copies were identified in some representatives of excavates, ciliates and amoebozoans. The presence of many Rab copies is correlated with significant differences in their expression level. The diversification of analysed Rab subfamilies is also manifested by non-conserved sequences and structural features, many of which are involved in the interaction with regulators and effectors. Individual sites discriminating different subgroups of Rab7 and Rab9 GTPases have been identified.

conclusionPhylogenetic reconstructions of Rab7 and Rab9 proteins were performed by a variety of methods. These Rab GTPases show diversification both at the phylogenetic, expression and structural levels. The presence of many Rab7 and Rab9 isoforms suggests their functional specialization and complexity of subcellular trafficking even in unicellular eukaryotes. The identified less conserved regions in analysed Rab sequences may directly contribute to such a differentiation.

Indexed as

Evolution, MolecularPhylogenyAmino Acid SequenceAnimalsConsensus SequenceGene ExpressionModels, GeneticMolecular Sequence DataProtein Structure, Secondaryrab7 GTP-Binding Proteinsrab GTP-Binding ProteinsSequence AlignmentSequence Analysis, DNArab7 GTP-Binding Proteinsrab GTP-Binding Proteins

Identifiers

PMID19442299
PMCPMC2693434
OpenAlexW2079936078

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.