Subcellular localization of Arabidopsis 3-hydroxy-3-methylglutaryl-coenzyme A reductase

dc.contributor.author
Leivar, Pablo
dc.contributor.author
Gonzalez, Victor Manuel
dc.contributor.author
Castel i Gil, Susanna
dc.contributor.author
Trelease, Richard N.
dc.contributor.author
López Iglesias, Carmen
dc.contributor.author
Arró i Plans, Montserrat
dc.contributor.author
Boronat i Margosa, Albert
dc.contributor.author
Campos Martínez, Narciso
dc.contributor.author
Ferrer i Prats, Albert
dc.contributor.author
Fernàndez Busquets, Xavier
dc.date.issued
2026-01-21T12:25:49Z
dc.date.issued
2026-01-21T12:25:49Z
dc.date.issued
2005-06-11
dc.date.issued
2026-01-21T12:25:49Z
dc.identifier
0032-0889
dc.identifier
https://hdl.handle.net/2445/225878
dc.identifier
519371
dc.description.abstract
Plants produce diverse isoprenoids, which are synthesized in plastids, mitochondria, endoplasmic reticulum (ER), and the nonorganellar cytoplasm. 3-Hydroxy-3-methylglutaryl-coenzyme A reductase (HMGR) catalyzes the synthesis of mevalonate, a rate-limiting step in the cytoplasmic pathway. Several branches of the pathway lead to the synthesis of structurally and functionally varied, yet essential, isoprenoids. Several HMGR isoforms have been identified in all plants examined. Studies based on gene expression and on fractionation of enzyme activity suggested that subcellular compartmentalization of HMGR is an important intracellular channeling mechanism for the production of the specific classes of isoprenoids. Plant HMGR has been shown previously to insert in vitro into the membrane of microsomal vesicles, but the final in vivo subcellular localization(s) remains controversial. To address the latter in Arabidopsis (<em>Arabidopsis thaliana</em>) cells, we conducted a multipronged microscopy and cell fractionation approach that included imaging of chimeric HMGR green fluorescent protein localizations in transiently transformed cell leaves, immunofluorescence confocal microscopy in wild-type and stably transformed seedlings, immunogold electron microscopy examinations of endogenous HMGR in seedling cotyledons, and sucrose density gradient analyses of HMGR-containing organelles. Taken together, the results reveal that endogenous Arabidopsis HMGR is localized at steady state within ER as expected, but surprisingly also predominantly within spherical, vesicular structures that range from 0.2- to 0.6-µm diameter, located in the cytoplasm and within the central vacuole in differentiated cotyledon cells. The N-terminal region, including the transmembrane domain of HMGR, was found to be necessary and sufficient for directing HMGR to ER and the spherical structures. It is believed, although not directly demonstrated, that these vesicle-like structures are derived from segments of HMGR-ER. Nevertheless, they represent a previously undescribed subcellular compartment likely capable of synthesizing mevalonate, which provides new evidence for multiorganelle compartmentalization of the isoprenoid biosynthetic pathways in plants.
dc.format
13 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
American Society of Plant Biologists
dc.relation
Versió postprint del document publicat a: https://doi.org/10.1104/pp.104.050245
dc.relation
Plant Physiology, 2005, vol. 137, num.1, p. 57-69
dc.relation
https://doi.org/10.1104/pp.104.050245
dc.rights
(c) American Society of Plant Biologists, 2005
dc.rights
info:eu-repo/semantics/openAccess
dc.subject
Enzimologia
dc.subject
Biologia molecular vegetal
dc.subject
Enzymology
dc.subject
Plant molecular biology
dc.title
Subcellular localization of Arabidopsis 3-hydroxy-3-methylglutaryl-coenzyme A reductase
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion


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