Levels of Lycopene b-Cyclase 1 Modulate Carotenoid Gene Expression and Accumulation in Daucus carota
Author
dc.contributor.author
Moreno, Juan Camilo
Author
dc.contributor.author
Pizarro, Lorena
es_CL
Author
dc.contributor.author
Fuentes, Paulina
es_CL
Author
dc.contributor.author
Handford, Michael
es_CL
Author
dc.contributor.author
Cifuentes Guzmán, Víctor
es_CL
Author
dc.contributor.author
Stange Klein, Claudia
es_CL
Admission date
dc.date.accessioned
2014-02-11T14:54:32Z
Available date
dc.date.available
2014-02-11T14:54:32Z
Publication date
dc.date.issued
2013
Cita de ítem
dc.identifier.citation
PLoS ONE 8(3): e58144
en_US
Identifier
dc.identifier.other
doi:10.1371/journal.pone.0058144
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/119771
General note
dc.description
Artículo de publicación ISI
en_US
Abstract
dc.description.abstract
Plant carotenoids are synthesized and accumulated in plastids through a highly regulated pathway. Lycopene b-cyclase
(LCYB) is a key enzyme involved directly in the synthesis of a-carotene and b-carotene through the cyclization of lycopene.
Carotenoids are produced in both carrot (Daucus carota) leaves and reserve roots, and high amounts of a-carotene and bcarotene
accumulate in the latter. In some plant models, the presence of different isoforms of carotenogenic genes is
associated with an organ-specific function. D. carota harbors two Lcyb genes, of which DcLcyb1 is expressed in leaves and
storage roots during carrot development, correlating with an increase in carotenoid levels. In this work, we show that
DcLCYB1 is localized in the plastid and that it is a functional enzyme, as demonstrated by heterologous complementation in
Escherichia coli and over expression and post transcriptional gene silencing in carrot. Transgenic plants with higher or
reduced levels of DcLcyb1 had incremented or reduced levels of chlorophyll, total carotenoids and b-carotene in leaves and
in the storage roots, respectively. In addition, changes in the expression of DcLcyb1 are accompanied by a modulation in the
expression of key endogenous carotenogenic genes. Our results indicate that DcLcyb1 does not possess an organ specific
function and modulate carotenoid gene expression and accumulation in carrot leaves and storage roots.