Dichotomy in the NRT gene families of dicots and grass species.

A large proportion of the nitrate (NO(3)(-)) acquired by plants from soil is actively transported via members of the NRT families of NO(3)(-) transporters. In Arabidopsis, the NRT1 family has eight functionally characterised members and predominantly comprises low-affinity transporters; the NRT2 fam...

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Autores principales: Darren Plett, John Toubia, Trevor Garnett, Mark Tester, Brent N Kaiser, Ute Baumann
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Publicado: Public Library of Science (PLoS) 2010
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spelling oai:doaj.org-article:02c5d53a3380457d8fc727dc410bc9232021-11-18T07:02:02ZDichotomy in the NRT gene families of dicots and grass species.1932-620310.1371/journal.pone.0015289https://doaj.org/article/02c5d53a3380457d8fc727dc410bc9232010-12-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21151904/?tool=EBIhttps://doaj.org/toc/1932-6203A large proportion of the nitrate (NO(3)(-)) acquired by plants from soil is actively transported via members of the NRT families of NO(3)(-) transporters. In Arabidopsis, the NRT1 family has eight functionally characterised members and predominantly comprises low-affinity transporters; the NRT2 family contains seven members which appear to be high-affinity transporters; and there are two NRT3 (NAR2) family members which are known to participate in high-affinity transport. A modified reciprocal best hit (RBH) approach was used to identify putative orthologues of the Arabidopsis NRT genes in the four fully sequenced grass genomes (maize, rice, sorghum, Brachypodium). We also included the poplar genome in our analysis to establish whether differences between Arabidopsis and the grasses may be generally applicable to monocots and dicots. Our analysis reveals fundamental differences between Arabidopsis and the grass species in the gene number and family structure of all three families of NRT transporters. All grass species possessed additional NRT1.1 orthologues and appear to lack NRT1.6/NRT1.7 orthologues. There is significant separation in the NRT2 phylogenetic tree between NRT2 genes from dicots and grass species. This indicates that determination of function of NRT2 genes in grass species will not be possible in cereals based simply on sequence homology to functionally characterised Arabidopsis NRT2 genes and that proper functional analysis will be required. Arabidopsis has a unique NRT3.2 gene which may be a fusion of the NRT3.1 and NRT3.2 genes present in all other species examined here. This work provides a framework for future analysis of NO(3)(-) transporters and NO(3)(-) transport in grass crop species.Darren PlettJohn ToubiaTrevor GarnettMark TesterBrent N KaiserUte BaumannPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 5, Iss 12, p e15289 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Darren Plett
John Toubia
Trevor Garnett
Mark Tester
Brent N Kaiser
Ute Baumann
Dichotomy in the NRT gene families of dicots and grass species.
description A large proportion of the nitrate (NO(3)(-)) acquired by plants from soil is actively transported via members of the NRT families of NO(3)(-) transporters. In Arabidopsis, the NRT1 family has eight functionally characterised members and predominantly comprises low-affinity transporters; the NRT2 family contains seven members which appear to be high-affinity transporters; and there are two NRT3 (NAR2) family members which are known to participate in high-affinity transport. A modified reciprocal best hit (RBH) approach was used to identify putative orthologues of the Arabidopsis NRT genes in the four fully sequenced grass genomes (maize, rice, sorghum, Brachypodium). We also included the poplar genome in our analysis to establish whether differences between Arabidopsis and the grasses may be generally applicable to monocots and dicots. Our analysis reveals fundamental differences between Arabidopsis and the grass species in the gene number and family structure of all three families of NRT transporters. All grass species possessed additional NRT1.1 orthologues and appear to lack NRT1.6/NRT1.7 orthologues. There is significant separation in the NRT2 phylogenetic tree between NRT2 genes from dicots and grass species. This indicates that determination of function of NRT2 genes in grass species will not be possible in cereals based simply on sequence homology to functionally characterised Arabidopsis NRT2 genes and that proper functional analysis will be required. Arabidopsis has a unique NRT3.2 gene which may be a fusion of the NRT3.1 and NRT3.2 genes present in all other species examined here. This work provides a framework for future analysis of NO(3)(-) transporters and NO(3)(-) transport in grass crop species.
format article
author Darren Plett
John Toubia
Trevor Garnett
Mark Tester
Brent N Kaiser
Ute Baumann
author_facet Darren Plett
John Toubia
Trevor Garnett
Mark Tester
Brent N Kaiser
Ute Baumann
author_sort Darren Plett
title Dichotomy in the NRT gene families of dicots and grass species.
title_short Dichotomy in the NRT gene families of dicots and grass species.
title_full Dichotomy in the NRT gene families of dicots and grass species.
title_fullStr Dichotomy in the NRT gene families of dicots and grass species.
title_full_unstemmed Dichotomy in the NRT gene families of dicots and grass species.
title_sort dichotomy in the nrt gene families of dicots and grass species.
publisher Public Library of Science (PLoS)
publishDate 2010
url https://doaj.org/article/02c5d53a3380457d8fc727dc410bc923
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