Rice Science ›› 2020, Vol. 27 ›› Issue (2): 152-161.DOI: 10.1016/j.rsci.2020.01.006
收稿日期:
2019-08-05
接受日期:
2019-11-13
出版日期:
2020-03-28
发布日期:
2019-11-28
. [J]. Rice Science, 2020, 27(2): 152-161.
Fig. 1. Expression profiles of rice starch synthesis genes during seed development in GLA4 and two endosperm mutants. GLA4, Guangluai 4. ADP-glucose pyrophosphorylase (ADPase) genes: AGPL1, AGPL2, AGPS1 and AGPS2b; Granule-bound starch synthase (GBSS) gene: GBSSI; Soluble starch synthase (SS) genes: SSI, SSIIa and SSIIIa; Branching enzyme (BE) genes: BEI, BEIIa and BEIIb; Debranching enzyme (DBE) genes: ISAI and PUL; Starch phosphorylase (SP) gene: SP.Total RNAs were extracted from developing seeds at 5, 10 and 15 d after flowering (DAF). Data are Mean ± SD from three replicates. The asterisks indicate statistical significance between GLA4 and the mutants, as determined by the Student’s t-test (*, P < 0.05; **, P < 0.01).
Fig. 2. Western blotting of starch synthetic enzymes extracted from developing endosperms of GLA4, GM077 and GM645 at 5, 10, 15 d after flowering (DAF) was performed using antisera against GBSSI, SSI, SSIIa, BEI, BEIIb and PUL from soluble proteins.A, Starch granule-bound protein for GBSSI blot. B, Soluble proteins for SSI, SSIIa, BEI, BEIIb and PUL enzymes blots. Values in the first line under the gel are mean relative levels to the GLA4 at 5 DAF, while those in the second lines are the standard deviation. GLA4, Guangluai 4.
Material | Reciprocal | One sided a | No signal | ||||
---|---|---|---|---|---|---|---|
Strong signal | Weak signal | Strong signal | Weak signal | ||||
GlA4 | SSI-SSIIa, SSI-BEIIb, SSI-PUL, SSIIa-BEI, SSIIa-BEIIb, BEI-BEIIb, BEI-PUL, BEIIb-PUL | SSI-BEI, PUL-SSIIa | |||||
GM077 | SSI-BEI*, SSI-BEIIb, SSIIa-BEI, SSIIa-BEIIb, SSIIa-PUL*, BEI-BEIIb, BEI-PUL, BEIIb-PUL | SSI-SSIIa* | SSI-PUL* | ||||
GM645 | SSI-BEIIb, SSI-PUL, BEI-PUL, BEIIb-PUL | SSI-SSIIa*, SSIIa-BEI*, SSIIa-BEIIb*, BEI-BEIIb* | SSIIa-PUL | SSI-BEI* |
Table 1 Comparison of protein-protein interactions among starch synthetic related enzymes in wild type and mutant endosperms determined by co-immunoprecipitation assay.
Material | Reciprocal | One sided a | No signal | ||||
---|---|---|---|---|---|---|---|
Strong signal | Weak signal | Strong signal | Weak signal | ||||
GlA4 | SSI-SSIIa, SSI-BEIIb, SSI-PUL, SSIIa-BEI, SSIIa-BEIIb, BEI-BEIIb, BEI-PUL, BEIIb-PUL | SSI-BEI, PUL-SSIIa | |||||
GM077 | SSI-BEI*, SSI-BEIIb, SSIIa-BEI, SSIIa-BEIIb, SSIIa-PUL*, BEI-BEIIb, BEI-PUL, BEIIb-PUL | SSI-SSIIa* | SSI-PUL* | ||||
GM645 | SSI-BEIIb, SSI-PUL, BEI-PUL, BEIIb-PUL | SSI-SSIIa*, SSIIa-BEI*, SSIIa-BEIIb*, BEI-BEIIb* | SSIIa-PUL | SSI-BEI* |
Fig. 3. Protein-protein interactions between starch synthetic related enzymes in wild type and mutant endosperms by co-immunoprecipitation (Co-IP).Black arrows represent the western blotting signals. M, Protein marker; a, Guangluai 4 (GLA4); b, GM077; c, GM645.
Fig. 4. Hypothesis models for starch synthesis in high amylose indica rice Guangluai 4 (GLA4) and two endosperm mutants. The predicted protein-protein complexes in developing seed of wild type indica rice GLA4 were demonstrated referring to Nakamura (2002); Nakamura et al (2005) and Fujita (2014). Only the difference in the protein-protein interactions in GM077 and GM645 from GLA4 was shown. Alterations of chain length distribution in GM077 and GM645 referred to Kong et al (2014). The small rounds of different color represent glucosyl residues from different starch synthases. DP, Degree of polymerization.
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