Os04g0682000 - Revision history

192.168.72.52: /* Structured Information */

2015-06-12T07:21:19Z

‎Structured Information

Xiaoshui: /* Annotated Information */

2014-06-10T03:14:22Z

‎Annotated Information

Xiaoshui: /* Annotated Information */

2014-06-10T03:13:43Z

‎Annotated Information

Xiaoshui: /* Annotated Information */

2014-06-10T03:12:13Z

‎Annotated Information

Xiaoshui: /* Annotated Information */

2014-06-10T03:10:15Z

‎Annotated Information

Xiaoshui: /* Annotated Information */

2014-06-10T03:00:59Z

‎Annotated Information

Xiaoshui: /* Annotated Information */

2014-06-10T03:00:11Z

‎Annotated Information

Xiaoshui: /* Annotated Information */

2014-06-10T02:59:18Z

‎Annotated Information

Xiaoshui: /* Function */

2014-06-10T02:56:21Z

‎Function

Xiaoshui: /* Function */

2014-06-10T02:55:16Z

‎Function

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 ==Structured Information==
 [[Category:Genes]]
 [[Category:Japonica mRNA]]

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 In addition to Atg8 lipidation, the deconjugation of Atg8 by Atg4 is also
 essential for autophagosome formation(3).In addition to ATG8s, When focus on Atg4 homologs, which may function in the C-terminal cleavage of ATG8s required for their modiﬁcation and in the deconjugation of their modiﬁed forms.As showed in Fig C, Two homologs of the ATG4 gene, ATG4a and 4b, were identiﬁed in the Arabidopsis genome (4).
 [[File:FF figure1.png]]
 [[File:FF figureB.png]]
 [[File:FF figure5.png]]
 ===Expression===

@@ Line 11: / Line 11: @@
 In addition to Atg8 lipidation, the deconjugation of Atg8 by Atg4 is also
 essential for autophagosome formation(3).In addition to ATG8s, When focus on Atg4 homologs, which may function in the C-terminal cleavage of ATG8s required for their modiﬁcation and in the deconjugation of their modiﬁed forms.As showed in Fig C, Two homologs of the ATG4 gene, ATG4a and 4b, were identiﬁed in the Arabidopsis genome (4).
+[[File:FF figure1.png]]
 [[File:FF figureB.png]]
 [[File:FF figure5.png]]
@@ Line 24: / Line 23: @@
 Proteinase ATG4 has several conservative cysteine residues in its structure, and can therefore serve as a redox sensor(6).
-[[File:FF figure1.png]]
+[[File:FF figureC.png]]
 [[File:FF figure3.png]]

@@ Line 12: / Line 12: @@
 essential for autophagosome formation(3).In addition to ATG8s, When focus on Atg4 homologs, which may function in the C-terminal cleavage of ATG8s required for their modiﬁcation and in the deconjugation of their modiﬁed forms.As showed in Fig C, Two homologs of the ATG4 gene, ATG4a and 4b, were identiﬁed in the Arabidopsis genome (4).
 ===Expression===
@@ Line 25: / Line 24: @@
 Proteinase ATG4 has several conservative cysteine residues in its structure, and can therefore serve as a redox sensor(6).
-[[File:FF figureB.png]]
+[[File:FF figure1.png]]
-[[File:FF figureC.png]]
+[[File:FF figure3.png]]

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 OsAtg4 shows low similarity to yeast and Arabidopsis Atg4, but the Cys-164,Asp-361 and His-361 of OsAtg4 are strictly conserved in all homologues(1), which constitute the conserved geometry observed in the canonical catalytic triad of cysteine protease(2). As shown in Figure B, sequence comparison of OsAtg4 (ABB77259) and its Arabidopsis (BAB88384, 56% identity), yeast (P53867, 26% identity) homologues. Identical residues are shaded in black, similarity residues are shaded in gray. The conserved residues are boxed(1).
-As showed in Fig. 5, Atg4 interacts with Atg8 and its mutants, indicating the conserved Gly117 mutation does not affect this interaction. This cleavage reaction may include two-step mechanism involving the recognition of the OsAtg8 core and the subsequent recognition of the OsAtg8 tail by OsAtg4. The tail region of OsAtg8 is crucial for hydrolysis, but it is not indispensable to the interaction between the core region of OsAtg8 and OsAtg4(1).
+As showed in Fig 5, Atg4 interacts with Atg8 and its mutants, indicating the conserved Gly117 mutation does not affect this interaction. This cleavage reaction may include two-step mechanism involving the recognition of the OsAtg8 core and the subsequent recognition of the OsAtg8 tail by OsAtg4. The tail region of OsAtg8 is crucial for hydrolysis, but it is not indispensable to the interaction between the core region of OsAtg8 and OsAtg4(1).
 In addition to Atg8 lipidation, the deconjugation of Atg8 by Atg4 is also
-essential for autophagosome formation(3).In addition to ATG8s, When focus on Atg4 homologs, which may function in the C-terminal cleavage of ATG8s required for their modiﬁcation and in the deconjugation of their modiﬁed forms. Two homologs of the ATG4 gene, ATG4a and 4b, were identiﬁed in the Arabidopsis genome (4).
+essential for autophagosome formation(3).In addition to ATG8s, When focus on Atg4 homologs, which may function in the C-terminal cleavage of ATG8s required for their modiﬁcation and in the deconjugation of their modiﬁed forms.As showed in Fig C, Two homologs of the ATG4 gene, ATG4a and 4b, were identiﬁed in the Arabidopsis genome (4).
@@ Line 17: / Line 17: @@
 [[File:FF figure3.png]]
 [[File:FF figure5.png]]
 ===Expression===
@@ Line 26: / Line 24: @@
 Proteinase ATG4 has several conservative cysteine residues in its structure, and can therefore serve as a redox sensor(6).

← Older revision		Revision as of 02:56, 10 June 2014
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	[[File:FF figure1.png]]		[[File:FF figure1.png]]
		+	[[File:FF figure3.png]]

	===Expression===		===Expression===

← Older revision		Revision as of 02:55, 10 June 2014
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		+
		+	[[File:FF figure1.png]]

	===Expression===		===Expression===