Difference between revisions of "Os03g0315400"

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(Labs working on this gene)
 
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==Annotated Information==
 
==Annotated Information==
 +
[[File:Real-time reverse-transcription (RT) PCR analysis for the expression of OsMYB2 in rice.jpg|right|thumb|327px|'''Figure 2.''' ''Real-time reverse-transcription (RT) PCR analysis for the expression of OsMYB2 in rice.<ref name="ref1" />.'']]
 +
 
===Gene Symbol===
 
===Gene Symbol===
 
*'''''Os03g0315400''''' '''<=>''' '''''OsMYB2,MYB2'''''
 
*'''''Os03g0315400''''' '''<=>''' '''''OsMYB2,MYB2'''''
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===Phenotypic analysis===
 
===Phenotypic analysis===
 
* No difference in growth and development between the OsMYB2-overexpressing and wild-type plants was observed under normal growth conditions, but the OsMYB2-overexpressing plants were more tolerant to salt, cold, and dehydration stresses and more sensitive to abscisic acid than wild-type plants.  
 
* No difference in growth and development between the OsMYB2-overexpressing and wild-type plants was observed under normal growth conditions, but the OsMYB2-overexpressing plants were more tolerant to salt, cold, and dehydration stresses and more sensitive to abscisic acid than wild-type plants.  
* The OsMYB2-overexpressing plants accumulated greater amounts of soluble sugars and proline than wild-type plants under salt stress. Overexpression of OsMYB2 enhanced up-regulation of genes encoding proline synthase and transporters. The OsMYB2-overexpressing plants accumulated less amounts of H 2 O 2 and malondialdehyde.  
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* The OsMYB2-overexpressing plants accumulated greater amounts of soluble sugars and proline than wild-type plants under salt stress. Overexpression of OsMYB2 enhanced up-regulation of genes encoding proline synthase and transporters. The OsMYB2-overexpressing plants accumulated less amounts of H2O2 and malondialdehyde.  
 
* The enhanced activities of antioxidant enzymes, including peroxidase, superoxide dismutase, and catalase, may underlie the lower H2O2 contents in OsMYB2-overexpressing plants.  
 
* The enhanced activities of antioxidant enzymes, including peroxidase, superoxide dismutase, and catalase, may underlie the lower H2O2 contents in OsMYB2-overexpressing plants.  
 
* There was greater up-regulation of stress-related genes, including OsLEA3, OsRab16A, and OsDREB2A, in the OsMYB2-overexpressing plants. Microarray analysis showed that expression of numerous genes involving diverse functions in stress response was altered in the OsMYB2-overexpressing plants.
 
* There was greater up-regulation of stress-related genes, including OsLEA3, OsRab16A, and OsDREB2A, in the OsMYB2-overexpressing plants. Microarray analysis showed that expression of numerous genes involving diverse functions in stress response was altered in the OsMYB2-overexpressing plants.
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===Expression===
 
===Expression===
 
* Expression of '''''OsMYB2''''' was up-regulated by salt, cold, and dehydration stress.
 
* Expression of '''''OsMYB2''''' was up-regulated by salt, cold, and dehydration stress.
[[File:Subcellular localization of OsMYB2.jpg]]
 
 
a、b、c: localization of GFP ;  e、d、f:localization of GFP-OsMYB2
 
 
The response of OsMYB2 expression to salt, cold, and
 
dehydration stress was monitored by real-time RT-PCR.
 
An increase in the OsMYB2 transcript was observed after
 
30 min of exposure to salt stress. The salt stress-induced
 
increase in the OsMYB2 transcript peaked after 5 h of salt
 
stress, and thereafter the transcript declined gradually under
 
salt stress . A similar increase in the OsMYB2
 
transcript was also observed when rice seedlings were
 
exposed to low temperature (2℃) or osmotic stress (20%
 
PEG) . In addition, treatment of rice seedlings with ABA
 
also led to an increase in expression of OsMYB2. In contrast,
 
exogenous application of salicylic acid reduced the expression of OsMYB2, while no effect of
 
indoleacetic acid and brassinosteroids on the OsMYB2
 
transcript was observed. OsMYB2 was detected in roots,
 
shoots, leaves, and flowers under non-stressed conditions,
 
with the expression being greatest in leaves, followed by
 
roots and shoots . The strong induction of this
 
gene by abiotic stress prompted this study to check its
 
promoter sequence (1500 bp upstream from the transcription
 
start site) by searching the promoter sequence against
 
the PLACE database [(http://www.dna.affrc.go.jp/PLACE/)].
 
The promoter of OsMYB2 contains stress-responsive related
 
cis-elements, such as ABRE and MYB and MYC
 
recognition sites
 
 
[[File:Real-time reverse-transcription (RT) PCR analysis for the expression of OsMYB2 in rice.jpg]]
 
  
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===Subcellular localization===
 +
* OsMYB2 was localized in the nucleus with transactivation activity.
 +
[[File:Subcellular localization of OsMYB2.jpg|center|thumb|727px|'''Figure 1.''' ''Subcellular localization and transactivation analysis of OsMYB2.<ref name="ref1" />.'']]
  
 
===Evolution===
 
===Evolution===
Phylogenetic tree of MYB proteins(figure 6).
+
* OsMYB2 representative by '''''LOC_Os3g20090''''' ('''''Os03g0315400''''') is belong to C12, and of which are involved in stress response.
 
 
 
 
[[File:Phylogenetic tree of MYB proteins.jpg]]
 
 
 
OsMYB2 representative by LOC_Os3g20090 is belong to C12, and of which are involved in stress response.
 
  
 
==Labs working on this gene==
 
==Labs working on this gene==

Latest revision as of 01:53, 14 February 2017

The rice Os03g0315400 was reported as OsMYB2 in 2012 [1] by researchers from China.

Annotated Information

Figure 2. Real-time reverse-transcription (RT) PCR analysis for the expression of OsMYB2 in rice.[1].

Gene Symbol

  • Os03g0315400 <=> OsMYB2,MYB2

Function

  • OsMYB2 encodes a stress-responsive MYB transcription factor.
  • OsMYB2 plays a regulatory role in tolerance of rice to salt, cold, and dehydration stress.

Phenotypic analysis

  • No difference in growth and development between the OsMYB2-overexpressing and wild-type plants was observed under normal growth conditions, but the OsMYB2-overexpressing plants were more tolerant to salt, cold, and dehydration stresses and more sensitive to abscisic acid than wild-type plants.
  • The OsMYB2-overexpressing plants accumulated greater amounts of soluble sugars and proline than wild-type plants under salt stress. Overexpression of OsMYB2 enhanced up-regulation of genes encoding proline synthase and transporters. The OsMYB2-overexpressing plants accumulated less amounts of H2O2 and malondialdehyde.
  • The enhanced activities of antioxidant enzymes, including peroxidase, superoxide dismutase, and catalase, may underlie the lower H2O2 contents in OsMYB2-overexpressing plants.
  • There was greater up-regulation of stress-related genes, including OsLEA3, OsRab16A, and OsDREB2A, in the OsMYB2-overexpressing plants. Microarray analysis showed that expression of numerous genes involving diverse functions in stress response was altered in the OsMYB2-overexpressing plants.

Expression

  • Expression of OsMYB2 was up-regulated by salt, cold, and dehydration stress.

Subcellular localization

  • OsMYB2 was localized in the nucleus with transactivation activity.
Figure 1. Subcellular localization and transactivation analysis of OsMYB2.[1].

Evolution

  • OsMYB2 representative by LOC_Os3g20090 (Os03g0315400) is belong to C12, and of which are involved in stress response.

Labs working on this gene

  • State Key Laboratory of Vegetation and Environmental Change, Institute of Botany, the Chinese Academy of Sciences, Beijing 100093, PR China
  • Graduate University of the Chinese Academy of Sciences, Beijing 100049, PR China

References

  1. 1.0 1.1 1.2 Yang A, Dai X, Zhang WH. A R2R3-type MYB gene, OsMYB2, is involved in salt, cold, and dehydration tolerance in rice. J Exp Bot. 2012 Apr;63(7):2541-56. doi: 10.1093/jxb/err431. PubMed PMID: 22301384; PubMed Central PMCID: PMC3346221.

Structured Information