ArticlePlant physiology1996
Sucrose Phosphate Synthase Expression at the Cell and Tissue Level Is Coordinated with Sucrose Sink-to-Source Transitions in Maize Leaf.
Article in Plant physiology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
7 citing papers in PubMed, 32 citations in OpenAlex.
- Functional definition of leaf sink-to-source transition by 14C tracing reveals transcriptional reprogramming in soybean.Plant & cell physiology · 2026Article
- Elements required for an efficient NADP-malic enzyme type C4 photosynthesis.Plant physiology · 2014Article
- Over-expression of AtPAP2 in Camelina sativa leads to faster plant growth and higher seed yield.Biotechnology for biofuels · 2012Article
- Structural and metabolic transitions of C4 leaf development and differentiation defined by microscopy and quantitative proteomics in maize.The Plant cell · 2010Article
- A small family of LLS1-related non-heme oxygenases in plants with an origin amongst oxygenic photosynthesizers.Plant molecular biology · 2004Article
- Tissue-specific and developmental pattern of expression of the rice sps1 gene.Plant physiology · 2000Article
- Sucrose-phosphate synthase steady-state mRNA increases in ripening kiwifruit.Plant molecular biology · 1998Article
Corrections and comments
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Authors and funding
3 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Immunohistological analyses for sucrose phosphate synthase (SPS) show that the protein is localized in both bundle-sheath cells (BS) and mesophyll cells (M) in maize (Zea mays) leaves. In young leaves, SPS protein was predominantly in the BS, whereas mature leaves showed nearly equal levels of signal in both BS and M. A cell-type-specific response was also seen in light and dark treatments. Dark treatments led to reduced signal in M; however, little or no change was detected in BS. We suggest that SPS in BS is engaged in sucrose biosynthesis by both photoassimilatory and starch turnover reactions in maize leaves. In addition, we suggest that the enzyme in BS may play a major role in the early biosynthesis of sucrose in young leaves. These cell-specific changes in expression in situ were in agreement with the estimates of extractable enzyme activity from isolated BS and M of mature leaves (R. Ohsugi, S.C. Huber [1987] Plant Physiol 84: 1096-1101). In contrast, western blot analyses did not show any significant changes in the levels of SPS protein in either young or mature leaves subsequent to similar dark treatments. It is interesting that the northern blot analyses indicate that the steady-state levels of SPS transcripts were markedly reduced after dark treatments of > 12 h. Overall, our results indicate that Sps gene expression in maize leaf is modulated at multiple levels of controls by both developmental and environmental factors.
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Registered trials
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