Os03g03150 - Revision history

Xiangjianhenwan: /* References */

2014-06-09T04:35:42Z

‎References

Xiangjianhenwan: /* References */

2014-06-09T04:10:40Z

‎References

Xiangjianhenwan: /* References */

2014-06-09T04:01:46Z

‎References

Xiangjianhenwan: /* References */

2014-06-09T03:59:33Z

‎References

Xiangjianhenwan: /* Mutation */

2014-06-09T03:19:00Z

‎Mutation

Xiangjianhenwan: /* Expression */

2014-06-09T03:18:40Z

‎Expression

Xiangjianhenwan: /* Mutation */

2014-06-08T11:13:54Z

‎Mutation

Xiangjianhenwan: /* Labs working on this gene */

2014-06-08T11:12:14Z

‎Labs working on this gene

Xiangjianhenwan: /* Expression */

2014-06-08T11:09:52Z

‎Expression

Xiangjianhenwan: /* Mutation */

2014-06-08T11:06:41Z

‎Mutation

@@ Line 56: / Line 56: @@
 . Marrocco, K., Thomann, A., Parmentier, Y., Genschik, P. & Criqui, M. C. The APC/C E3 ligase remains active in most post-mitotic Arabidopsis cells and is required for proper vasculature development and organization. Development 136, 1475–1485 (2009).
 . Eloy, N. B. et al. The APC/C subunit 10 plays an essential role in cell proliferation during leaf development. Plant J. 68, 351–363 (2011).
 . Kumar, M. et al. A candidate gene OsAPC6 of anaphase-promoting complex of rice identified through T-DNA insertion. Funct. Integr. Genomics 10, 349–358 (2010).
 . Kitamura, K., Maekawa, H. & Shimoda, C. Fission yeast Ste9, a homolog of Hct1/Cdh1 and Fizzy-related, is a novel negative regulator of cell cycle progression during G1-phase. Mol. Biol. Cell 9, 1065–1080 (1998).
 . Yamaguchi, S., Murakami, H. & Okayama, H. A WD repeat protein controls the cell cycle and differentiation by negatively regulating Cdc2/B-type cyclin complexes. Mol. Biol. Cell 8, 2475–2486 (1997).

@@ Line 52: / Line 52: @@
 . Capron, A. et al. The Arabidopsis anaphase-promoting complex or cyclosome: molecular and genetic characterization of the APC2 subunit. Plant Cell 15, 2370–2382 (2003).
 . Kwee, H. S. & Sundaresan, V. The NOMEGA gene required for female gametophyte development encodes the putative APC6/CDC16 component of the anaphase promoting complex in Arabidopsis. Plant J. 36, 853–866 (2003).
 == Additional information ==

@@ Line 42: / Line 42: @@
 . Cebolla, A. et al. The mitotic inhibitor ccs52 is required for endoreduplication and ploidy-dependent cell enlargement in plants. EMBO J. 18, 4476–4484 (1999).
 . Vinardell, J. M. et al. Endoreduplication mediated by the anaphase-promoting complex activator CCS52A is required for symbiotic cell differentiation in Medicago truncatula nodules. Plant Cell 15, 2093–2105 (2003).
 . Lammens, T. et al. Atypical E2F activity restrains APC/CCCS52A2 function obligatory for endocycle onset. Proc. Natl Acad. Sci. USA 105, 14721–14726 (2008).
 . Larson-Rabin, Z., Li, Z., Masson, P. H. & Day, C. D. FZR2/CCS52A1 expression is a determinant of endoreduplication and cell expansion in Arabidopsis. Plant Physiol. 149, 874–884 (2009).
 . Vanstraelen, M. et al. APC/CCCS52A complexes control meristem maintenance in the Arabidopsis root. Proc. Natl Acad. Sci. USA 106, 11806–11811 (2009).
@@ Line 52: / Line 52: @@
 . Capron, A. et al. The Arabidopsis anaphase-promoting complex or cyclosome: molecular and genetic characterization of the APC2 subunit. Plant Cell 15, 2370–2382 (2003).
 . Kwee, H. S. & Sundaresan, V. The NOMEGA gene required for female gametophyte development encodes the putative APC6/CDC16 component of the anaphase promoting complex in Arabidopsis. Plant J. 36, 853–866 (2003).

← Older revision		Revision as of 03:59, 9 June 2014
Line 39:		Line 39:
	7. Sigrist, S. J. & Lehner, C. F. Drosophila fizzy-related down-regulates mitotic cyclins and is required for cell proliferation arrest and entry into endocycles. Cell 90, 671–681 (1997).		7. Sigrist, S. J. & Lehner, C. F. Drosophila fizzy-related down-regulates mitotic cyclins and is required for cell proliferation arrest and entry into endocycles. Cell 90, 671–681 (1997).
	8. Li, M. et al. The adaptor protein of the anaphase promoting complex Cdh1 is essential in maintaining replicative lifespan and in learning and memory. Nat. Cell Biol. 10, 1083–1089 (2008).		8. Li, M. et al. The adaptor protein of the anaphase promoting complex Cdh1 is essential in maintaining replicative lifespan and in learning and memory. Nat. Cell Biol. 10, 1083–1089 (2008).
		+	9. Song, M. S. et al. Nuclear PTEN regulates the APC-CDH1 tumor-suppressive complex in a phosphatase-independent manner. Cell 144, 187–199 (2011).
		+	10. Cebolla, A. et al. The mitotic inhibitor ccs52 is required for endoreduplication and ploidy-dependent cell enlargement in plants. EMBO J. 18, 4476–4484 (1999).
		+	11. Vinardell, J. M. et al. Endoreduplication mediated by the anaphase-promoting complex activator CCS52A is required for symbiotic cell differentiation in Medicago truncatula nodules. Plant Cell 15, 2093–2105 (2003).
		+	12. Lammens, T. et al. Atypical E2F activity restrains APC/CCCS52A2 function obligatory for endocycle onset. Proc. Natl Acad. Sci. USA 105, 14721–14726 (2008).
		+	13. Larson-Rabin, Z., Li, Z., Masson, P. H. & Day, C. D. FZR2/CCS52A1 expression is a determinant of endoreduplication and cell expansion in Arabidopsis. Plant Physiol. 149, 874–884 (2009).
		+	14. Vanstraelen, M. et al. APC/CCCS52A complexes control meristem maintenance in the Arabidopsis root. Proc. Natl Acad. Sci. USA 106, 11806–11811 (2009).
		+	15. Mathieu-Rivet, E. et al. Functional analysis of the anaphase promoting complex activator CCS52A highlights the crucial role of endo-reduplication for fruit growth in tomato. Plant J. 62, 727–741 (2010).
		+	16. Boudolf, V. et al. CDKB1;1 forms a functional complex with CYCA2;3 to suppress endocycle onset. Plant Physiol. 150, 1482–1493 (2009).
		+	17. Heyman, J. et al. Arabidopsis ULTRAVIOLET-B-INSENSITIVE4 maintains cell division activity by temporal inhibition of the anaphase-promoting complex/cyclosome. Plant Cell 23, 4394–4410 (2011).
		+	18. Iwata, E. et al. GIGAS CELL1, a novel negative regulator of the anaphase-promoting complex/cyclosome, is required for proper mitotic progression and cell fate determination in Arabidopsis. Plant Cell 23, 4382–4393 (2011).
		+	19. Blilou, I. et al. The Arabidopsis HOBBIT gene encodes a CDC27 homolog that links the plant cell cycle to progression of cell differentiation. Genes Dev. 16, 2566–2575 (2002).
		+	20. Capron, A. et al. The Arabidopsis anaphase-promoting complex or cyclosome: molecular and genetic characterization of the APC2 subunit. Plant Cell 15, 2370–2382 (2003).
		+	21. Kwee, H. S. & Sundaresan, V. The NOMEGA gene required for female gametophyte development encodes the putative APC6/CDC16 component of the anaphase promoting complex in Arabidopsis. Plant J. 36, 853–866 (2003).

@@ Line 5: / Line 5: @@
 == Mutation==
-The tad1 mutant showed an increased tiller number, a reduced plant height, and twisted leaves and panicles[[File:Zhangyangyang.jpg]].
+The tad1 mutant showed an increased tiller number, a reduced plant height, and twisted leaves and panicles[[File:Zhangyangyang1.jpg]].
 Sequence analysis revealed a single base substitute (TGG→TGA) at the second exon of LOC_Os03g03150 in tad1, which produces a premature stop codon[[File:Zhangyangyang2.jpg]].

@@ Line 17: / Line 17: @@
 TAD1 is expressed ubiquitously in the examined rice organs, includ¬ing roots, shoot apices, axillary buds, internodes, nodes, and young leaves and panicles, but more abundant in young leaves, axillary buds and nodes[[File:Zhangyangyang3.jpg]].
 TAD1 was predominantly expressed in the leaf primordia and young leaves, tiller buds, inflorescence pro¬mordia, and crown root promordia. In addition, TAD1 expression was detected in vascular bundles at the unenlon¬gated stem[[File:Zhangyangyang4.jpg]].
-TAD1 has an oscillated expression pattern during the cell-cycle pro¬gression, showing a higher level in the G1-phase and a lower level in the S- and G2/M-phases. TAD1 most likely controls rice tillering through regulating MOC1. The 67-amino-acid N-terminal of TAD1 appears to be essential for its interaction with MOC1. TAD1 degrades MOC1 at the G1-phase. TAD1 recruits MOC1 to APC/C, and OsAPC10 is also involved in recognizing and target¬ing MOC1 for further degradation[[File:(Zhangyangyang5.jpg]].
+TAD1 has an oscillated expression pattern during the cell-cycle pro¬gression, showing a higher level in the G1-phase and a lower level in the S- and G2/M-phases. TAD1 most likely controls rice tillering through regulating MOC1. The 67-amino-acid N-terminal of TAD1 appears to be essential for its interaction with MOC1. TAD1 degrades MOC1 at the G1-phase. TAD1 recruits MOC1 to APC/C, and OsAPC10 is also involved in recognizing and target¬ing MOC1 for further degradation[[File:(Zhangyangyang5.jpg]]  [[File:Zhangyangyang6.jpg]].
 == Evolution ==

← Older revision		Revision as of 11:12, 8 June 2014
Line 27:		Line 27:
	1、State Key Laboratory of Plant Genomics and National Center for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.		1、State Key Laboratory of Plant Genomics and National Center for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
	2、State Key Laboratory of Rice Biology, China National Rice Research Institute, Chinese Academy of Agricultural Sciences, Hangzhou 310006, China.		2、State Key Laboratory of Rice Biology, China National Rice Research Institute, Chinese Academy of Agricultural Sciences, Hangzhou 310006, China.
		+
		+
		+	== References ==
		+
		+	1.Cebolla, A. et al. The mitotic inhibitor ccs52 is required for endoreduplication and ploidy-dependent cell enlargement in plants. EMBO J. 18, 4476–4484 (1999).
		+	2.Vinardell, J. M. et al. Endoreduplication mediated by the anaphase-promoting complex activator CCS52A is required for symbiotic cell differentiation in Medicago truncatula nodules. Plant Cell 15, 2093–2105 (2003).
		+	3. Kitamura, K., Maekawa, H. & Shimoda, C. Fission yeast Ste9, a homolog of Hct1/Cdh1 and Fizzy-related, is a novel negative regulator of cell cycle progression during G1-phase. Mol. Biol. Cell 9, 1065–1080 (1998).
		+	4. Yamaguchi, S., Murakami, H. & Okayama, H. A WD repeat protein controls the cell cycle and differentiation by negatively regulating Cdc2/B-type cyclin complexes. Mol. Biol. Cell 8, 2475–2486 (1997).
		+	5. Visintin, R., Prinz, S. & Amon, A. CDC20 and CDH1: a family of substrate-specific activators of APC-dependent proteolysis. Science 278, 460–463 (1997).
		+	6. Schwab, M., Lutum, A. S. & Seufert, W. Yeast Hct1 is a regulator of Clb2 cyclin proteolysis. Cell 90, 683–693 (1997).
		+	7. Sigrist, S. J. & Lehner, C. F. Drosophila fizzy-related down-regulates mitotic cyclins and is required for cell proliferation arrest and entry into endocycles. Cell 90, 671–681 (1997).
		+	8. Li, M. et al. The adaptor protein of the anaphase promoting complex Cdh1 is essential in maintaining replicative lifespan and in learning and memory. Nat. Cell Biol. 10, 1083–1089 (2008).

@@ Line 5: / Line 5: @@
 == Mutation==
-The tad1 mutant showed an increased tiller number, a reduced plant height, and twisted leaves and panicles(Zhangyangyang1).
+The tad1 mutant showed an increased tiller number, a reduced plant height, and twisted leaves and panicles(Zhangyangyang).
 Sequence analysis revealed a single base substitute (TGG→TGA) at the second exon of LOC_Os03g03150 in tad1, which produces a premature stop codon(Zhangyangyang2).