Evidence map›Paper›PMID 21447149›Full record

ArticleBMC evolutionary biology2011

Molecular evolution of urea amidolyase and urea carboxylase in fungi.

Pooja K Strope, Kenneth W Nickerson, Steven D Harris, Etsuko N Moriyama

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
6.0field-weighted citation impact, top 4% of its field
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 65 citations in OpenAlex.

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  10. First Report of Pathogenic BacteriumPathogens (Basel, Switzerland) · 2020
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4 · The record

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5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Pooja K StropeSchool of Biological Sciences, University of Nebraska, Lincoln, NE 68588, USA.
Kenneth W Nickerson
Steven D Harris
Etsuko N Moriyama
University of Nebraska–Lincoln · US

Funding

Efficient and Sensitive Mining System for G-Protein Coupled ReceptorsR01LM009219 · NLM · UNIVERSITY OF NEBRASKA LINCOLN · PI MORIYAMA, ETSUKO · 2007 to 2009
$672k
NLM NIH HHS R01LM009219
6 · The paper itself

Abstract

backgroundUrea amidolyase breaks down urea into ammonia and carbon dioxide in a two-step process, while another enzyme, urease, does this in a one step-process. Urea amidolyase has been found only in some fungal species among eukaryotes. It contains two major domains: the amidase and urea carboxylase domains. A shorter form of urea amidolyase is known as urea carboxylase and has no amidase domain. Eukaryotic urea carboxylase has been found only in several fungal species and green algae. In order to elucidate the evolutionary origin of urea amidolyase and urea carboxylase, we studied the distribution of urea amidolyase, urea carboxylase, as well as other proteins including urease, across kingdoms.

resultsAmong the 64 fungal species we examined, only those in two Ascomycota classes (Sordariomycetes and Saccharomycetes) had the urea amidolyase sequences. Urea carboxylase was found in many but not all of the species in the phylum Basidiomycota and in the subphylum Pezizomycotina (phylum Ascomycota). It was completely absent from the class Saccharomycetes (phylum Ascomycota; subphylum Saccharomycotina). Four Sordariomycetes species we examined had both the urea carboxylase and the urea amidolyase sequences. Phylogenetic analysis showed that these two enzymes appeared to have gone through independent evolution since their bacterial origin. The amidase domain and the urea carboxylase domain sequences from fungal urea amidolyases clustered strongly together with the amidase and urea carboxylase sequences, respectively, from a small number of beta- and gammaproteobacteria. On the other hand, fungal urea carboxylase proteins clustered together with another copy of urea carboxylases distributed broadly among bacteria. The urease proteins were found in all the fungal species examined except for those of the subphylum Saccharomycotina.

conclusionsWe conclude that the urea amidolyase genes currently found only in fungi are the results of a horizontal gene transfer event from beta-, gamma-, or related species of proteobacteria. The event took place before the divergence of the subphyla Pezizomycotina and Saccharomycotina but after the divergence of the subphylum Taphrinomycotina. Urea carboxylase genes currently found in fungi and other limited organisms were also likely derived from another ancestral gene in bacteria. Our study presented another important example showing plastic and opportunistic genome evolution in bacteria and fungi and their evolutionary interplay.

Indexed as

Evolution, MolecularBacteriaCarbon-Nitrogen LigasesFungiGene Transfer, HorizontalPhylogenyProtein Structure, TertiarySequence Homology, Amino AcidCarbon-Nitrogen Ligasesurea carboxylase (hydrolyzing)

Identifiers

PMID21447149
PMCPMC3073912
OpenAlexW2101193082

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LicenceCC BY
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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.