Plant Physiol, October 2000, Vol. 124, pp. 641-654
Tissue-Specific and Developmental Pattern of Expression of
the Rice sps1 Gene1
Ana T.
Chávez-Bárcenas,2
Juan J.
Valdez-Alarcón,23
Miguel
Martínez-Trujillo,
Lilly
Chen,
Beatriz
Xoconostle-Cázares,4
William
J.
Lucas, and
Luis
Herrera-Estrella*
Departamento de Ingeniería Genética de Plantas,
Centro de Investigación y de Estudios Avanzados del Instituto
Politécnico Nacional, Unidad Irapuato, Irapuato, Guanajuato,
Mexico (A.T.C.-B., J.J.V.-A., M.M.-T., L.H.-E.); International
Laboratory of Tropical Agricultural Biotechnology, The Scripps Research
Institute, La Jolla, California (L.C.); and Division of Biological
Sciences, University of California, Davis, California (B.X.-C.,
W.J.L.)
Sucrose-phosphate synthase (SPS) is one of the key regulatory
enzymes in carbon assimilation and partitioning in plants. SPS plays a
central role in the production of sucrose in photosynthetic cells and
in the conversion of starch or fatty acids into sucrose in germinating
seeds. To explore the mechanisms that regulate the tissue-specific and
developmental distribution of SPS, the expression pattern of rice
(Oryza sativa) sps1 (GenBank accession no. U33175) was examined by in situ reverse transcriptase-polymerase chain reaction and the expression directed by the sps1
promoter using the
-glucuronidase reporter gene. It was found that
the expression of the rice sps1 gene is limited to
mesophyll cells in leaves, the scutellum of germinating seedlings, and
pollen of immature inflorescences. During leaf development, the
sps1 promoter directs a basipetal pattern of expression
that coincides with the distribution of SPS activity during the leaf
sink-to-source transition. It was also found that during the vegetative
part of the growth cycle, SPS expression and enzymatic activity are highest in the youngest fully expanded leaf. Additionally, it was
observed that the expression of the sps1 promoter is
regulated by light and dependent on plastid development in
photosynthetic tissues, whereas expression in scutellum is independent
of both light and plastid development.
1
This work was supported in part by the
Howard-Hughes Biomedical Institute (grant no. 75191-526901 to
L.H.-E.), the Rockefeller Foundation (grant no. 90032-65 to L.H.-E.),
and the National Science Foundation (grant no. IBN-99-00539 to
W.J.L.). A.T.C.-B. and J.J.V.-A. were doctoral fellows from the Consejo
Nacional de Ciencia y Tecnología (Mexico).
2
These authors contributed equally to the paper.
3
Present address: Centro de Investigaciones en Ciencias
Microbiológicas, Instituto de Ciencias, Benemérita
Universidad Autónoma de Puebla, 72000, Puebla, Mexico.
4
Present address: Departamento de Biotecnología y
Bioingeniería, Centro de Investigación y de Estudios
Avanzados del I.P.N., Unidad Zacatenco, Av. Instituto Politécnico
Nacional 2508, 07000, Mexico.
*
Corresponding author; e-mail
lherrera{at}irapuato.ira.cinvestav.mx; fax 52-4-6245849.
© 2000 American Society of Plant Physiologists