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@ARTICLE{Rosar:17105,
author = {Rosar, C. and Kanonenberg, K. and Nanda, A.M. and
Mielewczik, M. and Bräutigam, A. and Novák, O. and
Strnade, M. and Walter, A. and Weber, A.P.M.},
title = {{T}he {L}eaf {R}eticulate {M}utant dov1 {I}s {I}mpaired in
the {F}irst {S}tep of {P}urine {M}etabolism},
journal = {Molecular plant},
issn = {1674-2052},
address = {Oxford},
publisher = {Oxford Univ. Press},
reportid = {PreJuSER-17105},
year = {2012},
note = {Record converted from VDB: 12.11.2012},
abstract = {A series of reticulated Arabidopsis thaliana mutants were
previously described. All mutants show a reticulate leaf
pattern, namely green veins on a pale leaf lamina. They have
an aberrant mesophyll structure but an intact layer of
bundle sheath cells around the veins. Here, we unravel the
function of the previously described reticulated EMS-mutant
dov1 (differential development of vascular associated cells
1). By positional cloning, we identified the mutated gene,
which encodes glutamine phosphoribosyl pyrophosphate
aminotransferase 2 (ATase2), an enzyme catalyzing the first
step of purine nucleotide biosynthesis. dov1 is allelic to
the previously characterized cia1-2 mutant that was isolated
in a screen for mutants with impaired chloroplast protein
import. We show that purine-derived total cytokinins are
lowered in dov1 and crosses with phytohormone reporter lines
revealed differential reporter activity patterns in dov1.
Metabolite profiling unraveled that amino acids that are
involved in purine biosynthesis are increased in dov1. This
study identified the molecular basis of an established
mutant line, which has the potential for further
investigation of the interaction between metabolism and leaf
development.},
cin = {IBG-2},
ddc = {580},
cid = {I:(DE-Juel1)IBG-2-20101118},
pnm = {Terrestrische Umwelt},
pid = {G:(DE-Juel1)FUEK407},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:22532604},
UT = {WOS:000312573500010},
doi = {10.1093/mp/sss045},
url = {https://juser.fz-juelich.de/record/17105},
}