Difference between revisions of "Os02g0491300"
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| − | + | The rice '''''Os02g0491300''''' was reported as '''''MTR1''''' in 2012 <ref name="ref1" /> by researchers from China. | |
==Annotated Information== | ==Annotated Information== | ||
| + | ===Gene Symbol=== | ||
| + | *'''''Os02g0491300''''' '''''<=>''''' '''''OsMTR1''''','''''MTR1''''' | ||
| + | [[File:221-Os02g0491300.png|right|thumb|427px|'''Figure 1.''' ''Phenotypic Analysis of mtr1 Anthers.<ref name="ref1" />.'']] | ||
===Function=== | ===Function=== | ||
| − | + | * MICROSPORE AND TAPETUM REGULATOR1 ('''''MTR1''''') is a rice fascilin glycoprotein protein. | |
| − | MICROSPORE AND TAPETUM REGULATOR1 (MTR1) is a rice fascilin glycoprotein protein. | + | * '''''MTR1''''' may act as an extracellular adhesion molecule in male reproductive development by regulating the cell-to-cell communication between reproductive cells and their adjacent somatic cells. |
| − | + | * '''''MTR1''''' can controll the development of sporophytic and reproductive cells in rice (Oryza sativa). | |
| − | * an essential gene for programmed tapetal cell fate and pollen formation in rice. | + | * '''''MTR1''''' is an essential gene for programmed tapetal cell fate and pollen formation in rice. |
| − | + | * '''''MTR1''''' is required for both the development of the diploid anther wall cells and maturation of the postmeiotic haploid microspores. | |
| − | * is required for both the development of the diploid anther wall cells and maturation of the postmeiotic haploid microspores. | + | * '''''MTR1''''' effect the deposition of sporopollenin precursors on the surface. |
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| − | * effect the deposition of sporopollenin precursors on the surface. | ||
===Gene Structure=== | ===Gene Structure=== | ||
| − | + | * ''MTR1'' locus was located on chromosome 2 between two InDel markers, TH239 and TH234. The MTR1 transcript is approximately 2 kb in length and contains a 1,752 bp coding sequence without any intron, a 55 bp 5' untranslated region (UTR) and a 193 bp 3' UTR. | |
| − | + | * The predicted MTR1 protein is 583 amino acids long and contains a putative N-terminal signal peptide; two fasciclin domains (amino acids 257–356 and 435–535); and two potential N-glycosylation sites (amino acids 433 and 554). | |
| − | ''MTR1'' locus was located on chromosome 2 between two InDel markers, TH239 and TH234. The MTR1 transcript is approximately 2 kb in length and | + | [[File:MTR4.jpg|right|thumb|427px|'''Figure 6.''' ''Map-Based Cloning analysis of MTR1<ref name="ref1" />.'']] |
| − | contains a 1,752 bp coding sequence without any intron, a 55 bp 5' untranslated region (UTR) and a 193 bp 3' UTR. The predicted MTR1 protein is | ||
| − | 583 amino acids long and contains a putative N-terminal signal peptide; two fasciclin domains (amino acids 257–356 and 435–535); and two potential N-glycosylation sites (amino acids 433 and 554). | ||
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| − | [[File:MTR4.jpg]] | ||
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===Mutation and Phenotype=== | ===Mutation and Phenotype=== | ||
| − | + | * mtr1 shows normal vegetative and nonreproductive floral organ development, but has smaller and pale-yellow anthers that fail to produce viable pollen grains (Figures S1A–S1F available online; Figures 1A and 1B). | |
| − | + | * All the F1 progeny from the backcross between wild-type and mtr1 displayed the wide-type phenotype, and the F 2 progeny yielded a segregation of 481 wild-type and 147 mutant plants (c 2 = 0.85,p > 0.05), suggesting a monofactorial recessive inheritance of the mutation. | |
| − | + | * To characterize the defects of anther development in mtr1, researchers performed 4 0 ,6-diamidino-2-phenylindole (DAPI) staining of microspores. | |
| − | + | # At stage 8b of anther development, mtr1 produced normal tetrads just like the wild-type (Figures 1C and 1D). However, at stages 9 and 10, after the microspores were released from the tetrad, mtr1 microspores expanded much more slowly than those of the wild-type (Figures 1E–1H). | |
| − | + | # At later stages, each wild-type microspore underwent mitosis, gener- ating the mature trinucleate pollen grain that contains two smaller sperm nuclei and a larger vegetative nucleus (Figures 1I and 1K). | |
| − | + | # By contrast, mtr1 microspores continued to show slow development, did not seem to go through mitosis, and were eventually aborted (Figures 1J and 1L). | |
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==Labs working on this gene== | ==Labs working on this gene== | ||
| − | + | * State Key Laboratory of Hybrid Rice, School of Life Sciences and Biotechnology Center, Key Laboratory of Genetics & Development and | |
| + | * Department of Energy Plant Research Laboratory, Michigan State University, East Lansing, MI 48824, USA | ||
==References== | ==References== | ||
| − | + | <references> | |
| + | * <ref name="ref1"> | ||
| + | Tan H, Liang W, Hu J, Zhang D. MTR1 encodes a secretory fasciclin glycoprotein | ||
| + | required for male reproductive development in rice. Dev Cell. 2012 Jun | ||
| + | 12;22(6):1127-37. doi: 10.1016/j.devcel.2012.04.011. PubMed PMID: 22698279. | ||
| + | </ref> | ||
| + | </references> | ||
==Structured Information== | ==Structured Information== | ||
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[[Category:Genes]] | [[Category:Genes]] | ||
[[Category:Japonica mRNA]] | [[Category:Japonica mRNA]] | ||
Latest revision as of 09:07, 14 February 2017
The rice Os02g0491300 was reported as MTR1 in 2012 [1] by researchers from China.
Contents
Annotated Information
Gene Symbol
- Os02g0491300 <=> OsMTR1,MTR1
Figure 1. Phenotypic Analysis of mtr1 Anthers.[1].
Function
- MICROSPORE AND TAPETUM REGULATOR1 (MTR1) is a rice fascilin glycoprotein protein.
- MTR1 may act as an extracellular adhesion molecule in male reproductive development by regulating the cell-to-cell communication between reproductive cells and their adjacent somatic cells.
- MTR1 can controll the development of sporophytic and reproductive cells in rice (Oryza sativa).
- MTR1 is an essential gene for programmed tapetal cell fate and pollen formation in rice.
- MTR1 is required for both the development of the diploid anther wall cells and maturation of the postmeiotic haploid microspores.
- MTR1 effect the deposition of sporopollenin precursors on the surface.
Gene Structure
- MTR1 locus was located on chromosome 2 between two InDel markers, TH239 and TH234. The MTR1 transcript is approximately 2 kb in length and contains a 1,752 bp coding sequence without any intron, a 55 bp 5' untranslated region (UTR) and a 193 bp 3' UTR.
- The predicted MTR1 protein is 583 amino acids long and contains a putative N-terminal signal peptide; two fasciclin domains (amino acids 257–356 and 435–535); and two potential N-glycosylation sites (amino acids 433 and 554).
Figure 6. Map-Based Cloning analysis of MTR1[1].
Mutation and Phenotype
- mtr1 shows normal vegetative and nonreproductive floral organ development, but has smaller and pale-yellow anthers that fail to produce viable pollen grains (Figures S1A–S1F available online; Figures 1A and 1B).
- All the F1 progeny from the backcross between wild-type and mtr1 displayed the wide-type phenotype, and the F 2 progeny yielded a segregation of 481 wild-type and 147 mutant plants (c 2 = 0.85,p > 0.05), suggesting a monofactorial recessive inheritance of the mutation.
- To characterize the defects of anther development in mtr1, researchers performed 4 0 ,6-diamidino-2-phenylindole (DAPI) staining of microspores.
- At stage 8b of anther development, mtr1 produced normal tetrads just like the wild-type (Figures 1C and 1D). However, at stages 9 and 10, after the microspores were released from the tetrad, mtr1 microspores expanded much more slowly than those of the wild-type (Figures 1E–1H).
- At later stages, each wild-type microspore underwent mitosis, gener- ating the mature trinucleate pollen grain that contains two smaller sperm nuclei and a larger vegetative nucleus (Figures 1I and 1K).
- By contrast, mtr1 microspores continued to show slow development, did not seem to go through mitosis, and were eventually aborted (Figures 1J and 1L).
Labs working on this gene
- State Key Laboratory of Hybrid Rice, School of Life Sciences and Biotechnology Center, Key Laboratory of Genetics & Development and
- Department of Energy Plant Research Laboratory, Michigan State University, East Lansing, MI 48824, USA
