Difference between revisions of "Os03g0427300"

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(Mutation)
(References)
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Simpson, D.J., G.B. Fincher, A.H.C. Huang and V. Cameron-Mills (2003) Structure and function of cereal and related higher plant (1→4)-beta-xylan endohydrolases. J. Cereal Sci. 37: 111–127.
 
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==Structured Information==
 
==Structured Information==
 
     [[Category:Genes]][[Category:Oryza Sativa Japonica Group]][[Category:Japonica Chromosome 3]]
 
     [[Category:Genes]][[Category:Oryza Sativa Japonica Group]][[Category:Japonica Chromosome 3]]

Revision as of 03:44, 5 August 2016

Glup4 gene encodes small GTPase, Rab5a in rice[1].

Annotated Information

Function

Mutation

  • Using RT-PCR in the presence of dUTPOregon Green to label RNAs and rhodamine B hexyl ester to stain prolamine protein bodies, glutelin RNAs are found to be preferentially transported to the cisternal-ER (Cis-ER) in wildtype endosperm (Fig. 1). Prolamine RNAs, on the other hand, are targeted to ER that delimits the spherical prolamine protein bodies (PB-ER). In the glup4 mutant, however, glutelin RNAs are partially misdirected from the Cis-ER to the PB-ER (Fig. 1), as well as to large dilated multivesicular body-like structures located near the plasma membrane (data not shown). The glutelin RNA mistargeting was not only observed in one gene (Gt-2), but also in others (GluA-1, GluA- 3 and GluB-1, data not shown). Prolamine RNA localization to the PB-ER is unaffected (Fig. 1), suggesting that Rab5 is involved in glutelin RNA sorting only[2].
Fig. 1. Localization of prolamine and glutelin mRNAs in wildtype and glup4 developing rice endosperm. [2].
  • Microarray analysis of transcripts isolated from glup4 and wildtype developing seeds identified 35 transcripts that

were upregulated and 10 that were downregulated by at least 2-fold in the glup4 mutant using a stringent P value (<0.001) to avoid false positives (Table 1 and Table 2)[2].

Table 1. Transcripts upregulated in the glup4 mutant compared to wildtype (P < 0.001) [2].
Table 2. Transcripts downregulated in the glup4 mutant compared to wildtype (P < 0.001) [2].
  • The researchers utilized

2D-DIGE to analyze the protein expression profiles of soluble extracts from 12–14 DAF wildtype and glup4 rice seeds (Fig. 3). Twenty-one protein spots were found to be differentially expressed (P < 0.05) with at least a 2-fold change in expression when analyzed on pH 3–10 non-linear immobilized pH gradient strips. Only two proteins were found to have at least a 2-fold increase in expression in the glup4 mutant (Table 3). One of these proteins, annotated as a glycosyl hydrolase, has similarity to xylanase inhibitor (XI) proteins, which function in cell wall restructuring[3]. Although not the same protein, xylanase inhibitor TAXI-VI mRNA was also found to be upregulated in the mutant (Table 1).

Expression Pattern

Evolution

Subcellular localization

Labs working on this gene

  • Institute of Biological Chemistry, Washington State University, Pullman WA, 99164-6340 USA
  • Faculty of Agriculture, Kyushu University, 6-10-1 Hakozaki, Fukuoka 812-8581, Japan
  • School of Molecular Biosciences, Washington State University, Pullman WA, 99164-7520 USA
  • Present Address: International Liberal Arts Program, Akita International University, Akita 010-1292, Japan
  • Present Address: Laboratory of Plant Molecular Genetics, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0101, Japan

References

  1. Satoh-Cruz M, Fukuda M, Ogawa M, et al. Glup4 gene encodes small GTPase, Rab5a in rice[J]. Rice Genet Newsl, 2010, 25: 48-49.
  2. 2.0 2.1 2.2 2.3 2.4 Doroshenk K A, Crofts A J, Washida H, et al. Characterization of the rice glup4 mutant suggests a role for the small GTPase Rab5 in the biosynthesis of carbon and nitrogen storage reserves in developing endosperm[J]. Breeding science, 2010, 60(5): 556-567.
  3. Simpson, D.J., G.B. Fincher, A.H.C. Huang and V. Cameron-Mills (2003) Structure and function of cereal and related higher plant (1→4)-beta-xylan endohydrolases. J. Cereal Sci. 37: 111–127.

Structured Information