Difference between revisions of "Os11g0685700"

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===Evolution===
 
===Evolution===
Multiple domain acquisition and loss events appear to have shaped the WRKY family. Numerous WRKY gene duplications occurred after the divergence of the monocotyledons from dicotyledons some 50–80 million years ago. The WRKY domains are found in expressed sequence tags (ESTs) from over 40 species of land plants.
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Multiple domain acquisition and loss events appear to have shaped the WRKY family. Numerous WRKY gene duplications occurred after the divergence of the monocotyledons from dicotyledons some 50–80 million years ago. The WRKY domains are found in expressed sequence tags (ESTs) from over 40 species of land plants.There is no evidence for WRKY genes in the archaea,eubacteria, the eukaryotic fungi, or animal lineages. However,a single WRKY gene with two WRKY domains exists in thegenomes of the protist Giardia lamblia and the slime mold Dictyostelium discoideum.the WRKY family may occur in primitive eukaryotes, before the emergence of the plant phyla, and its gross expansion during the course of plant evolutionary radiation, likely because of selective pressures favoring greater adaptability.The presence of a group I WRKY protein in these ancient organisms suggests that group I WRKY genes represent the ancestral form, with other groups arising later through losses and gains of a WRKY domain, and that this family originated some 1.8–2 billion years ago.Only group Ia genes, but not group Ib genes, appear to be derived from ancestral forms of the WRKY genes in plants.
 
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Researchers find evidence of loss of the N-terminus in the evolution of single-domain group II and group IV genes from group Ia genes and independent loss of the C-terminus in the evolution of a single-domain group II gene. Other group II genes may have evolved by this process.The group Ib OsWRKY genes are likely to have evolved by intramolecular duplication of a group III WRKY domain that had already evolved the C2HC type zinc-finger.Figure 2 shows that there is a difference between N- and C-terminal WRKY domains for those WRKY proteins with two WRKY domains. These domains tend to cluster into discrete groupings and there is more variability among the N- than the C-terminal WRKY domains. In the WRKY protein,the C-terminal domains are required for DNA-binding activity, thus are constrained in their ability to mutate without losing function, whereas the N-terminal domains mediate protein-protein interactions and may be less functionally constrained. The group II rice WRKY genes arose from the two-domain group Ia WRKY genes through a single domain loss event. The group Ib genes were derived from group III by domain duplication. The C- and N-terminal domains of group Ib genes are exclusively clustered with those of group 3 genes. The group Ia genes arose from a fusion of two group II WRKY genes evolved at an early time.The WRKY80 domain may represent the extant descendent of the group Ia C-terminal progenitor and WRKY57 a descendent of the N-terminal progenitor.
  
  

Revision as of 04:32, 10 June 2014

Annotated Information

Function

1,Roles in disease resistance and responses to salicylic acid: The major role of WRKY genes in flowering plants is to mediate defense responses.WRKY18, WRKY40, and WRKY60 form both homocomplexes and heterocomplexes to regulate Arabidopsis responses to the hemibiotrophic bacterial pathogen Pseudomonas syringae and the necrotrophic fungal pathogen Botrytis cinerea.An indica rice WRKY gene, which is identical to OsWRKY12,is induced by the bacterial pathogen Xanthomonas oryzae pv. oryzae.For japonica, an analysis of OsWRKY genes revealed that the expression level of 15 WRKY genes is increased in an interaction between rice and Magnaporthe frisea, a fungal pathogen that causes devastating rice blast disease. Besides,the expression of two OsWRKY genes was increased in SA-treated leaves and that of three OsWRKY genes was increased by jasmonic acid (JA) treatment.

2.Roles in seed development and germination: MINI3 encodes WRKY10, a WRKY class transcription factor, which is responsible for seed growth and development. Besides, two WRKY genes are induced during somatic embryo genesis of orchardgrass. The products of WRKY genes, which named SUSIBA2,is a regulatory transcription factor in starch synthesis. OsWRKY51 and OsWRKY71 are two ABA-inducible and gibberellin (GA)-repressible rice WRKY genes, which mediate the cross-talk of GA and ABA signaling,can repress the expression of α- amylase gene, as the figure shows. TTG2,a group I WRKY protein is also responsible for trichome development and mucilage production in the seed coat of rice. What's more,WRKY genes is also involved in the process of senescence.Arabidopsis AtWRKY53 is expressed in an age-dependent manner and, when overexpressed, leads to early flowering and senescence. Tang1.jpg

3,Roles in responses to abiotic stresses and ABA: In the desert plant Retama raetam, a WRKY gene was only induced when the plant was exposed to a combination of heat shock and drought.Several rice WRKY genes to be capable of regulating the ABA-inducible HVA22 promoter in a positive(OsWRKY72 and -77) or negative (OsWRKY24 and -45) manner.A dozen rice WRKY genes are induced by heat shock, cold stress, high salinity, and polyethylene glycol.Hv-WRKY38,the ortholog of OsWRKY51 and -71 ,is upregulated in response to drought and cold in vegetative tissues. Moreover,OsWRKY71 was upregulated by SA,JA, 1-aminocyclo-propane-1-carboxylic acid (ACC), wounding, and pathogen infection. Overexpression of OsWRKY71 in rice resulted in enhanced resistance to virulent Xoo 13751.

4,Roles in the biosynthesis of secondary metabolites: WRKY genes regulate the biosynthesis of sesquiterpene and benzylisoquinoline alkaloid.CjWRKY1 in C. japonica protoplasts was found to be responsible for the level of transcripts of berberine biosynthetic genes.

Evolution

Multiple domain acquisition and loss events appear to have shaped the WRKY family. Numerous WRKY gene duplications occurred after the divergence of the monocotyledons from dicotyledons some 50–80 million years ago. The WRKY domains are found in expressed sequence tags (ESTs) from over 40 species of land plants.There is no evidence for WRKY genes in the archaea,eubacteria, the eukaryotic fungi, or animal lineages. However,a single WRKY gene with two WRKY domains exists in thegenomes of the protist Giardia lamblia and the slime mold Dictyostelium discoideum.the WRKY family may occur in primitive eukaryotes, before the emergence of the plant phyla, and its gross expansion during the course of plant evolutionary radiation, likely because of selective pressures favoring greater adaptability.The presence of a group I WRKY protein in these ancient organisms suggests that group I WRKY genes represent the ancestral form, with other groups arising later through losses and gains of a WRKY domain, and that this family originated some 1.8–2 billion years ago.Only group Ia genes, but not group Ib genes, appear to be derived from ancestral forms of the WRKY genes in plants. Researchers find evidence of loss of the N-terminus in the evolution of single-domain group II and group IV genes from group Ia genes and independent loss of the C-terminus in the evolution of a single-domain group II gene. Other group II genes may have evolved by this process.The group Ib OsWRKY genes are likely to have evolved by intramolecular duplication of a group III WRKY domain that had already evolved the C2HC type zinc-finger.Figure 2 shows that there is a difference between N- and C-terminal WRKY domains for those WRKY proteins with two WRKY domains. These domains tend to cluster into discrete groupings and there is more variability among the N- than the C-terminal WRKY domains. In the WRKY protein,the C-terminal domains are required for DNA-binding activity, thus are constrained in their ability to mutate without losing function, whereas the N-terminal domains mediate protein-protein interactions and may be less functionally constrained. The group II rice WRKY genes arose from the two-domain group Ia WRKY genes through a single domain loss event. The group Ib genes were derived from group III by domain duplication. The C- and N-terminal domains of group Ib genes are exclusively clustered with those of group 3 genes. The group Ia genes arose from a fusion of two group II WRKY genes evolved at an early time.The WRKY80 domain may represent the extant descendent of the group Ia C-terminal progenitor and WRKY57 a descendent of the N-terminal progenitor.


Structured Information

Gene Name

Os11g0685700

Description

Oryza sativa (indica cultivar-group) WRKY transcription factor 61 (WRKY61) gene

Version

GI:46394376

Length

986 bp

Definition

TPA_inf: Oryza sativa (indica cultivar-group) WRKY transcription factor 61 (WRKY61) gene, complete cds.

Source

Oryza sativa Indica Group (long-grained rice)

 ORGANISM  Oryza sativa Japonica Group
           Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;
           Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP
           clade; Ehrhartoideae; Oryzeae; Oryza.
Chromosome

{{{Chromosome}}}

Location

{{{AP}}}

Sequence Coding Region

1..113,284..574,674..986

Expression

GEO Profiles:Os11g0685700

Genome Context

{{{GCID}}}

Gene Structure

{{{GSID}}}

Coding Sequence

<cdnaseq> 1 atggaaagaa ggaaggtgat caggatgagt tatacagagg atgacggctt cagctggagg

     61 aagtacgggc agaaggacgt ggaaggcgcc atgcacccaa ctacccaaag taa
     241                                           aagttat ttccgatgtg
     301 cccacaagat gacgacgggc tgtaaggcac ggaagaaggt gcagcgcacc gacggcgacc
     361 cgctgatggt cgacgtcgta tacaaggggg ttcacagctg tgccggcgtg cattccgaca
     421 gccagagatc atccgccgcg agctctaagt ctaacctgcg gccgacgaag agcatgcagg
     481 tgagggcgag ctccaaggac gtcggccccc cagacgacgg ttacagctgg aagaggtacg
     541 gccagaagaa catcttcggc gctaattacc caag
     661             atgctac taccggtgta tacacaagac cacgacgggc tgcactgcga
     721 caaaaaatgc acaggccacc gatggtgacc cactcctctt cgacgtcgtg taccacgggg
     781 agcacacctg cgatctgcag agcacgcact ccaacgacgt cgaaccgatc aggccgcagt
     841 ctgggctcga cgacgacatg tgtaccgacg atacgacgac tgtctccaca cgccacgaca
     901 gcaacacgga tgcgtcctca attagttttc aattagattg gaccaattgc aaagacgaat
     961 cggatggccc tcccaccacc ctataa

</cdnaseq>

Protein Sequence

<aaseq>MERRKVIRMSYTEDDGFSWRKYGQKDVEGAMHPTTQSKSYFRCA

HKMTTGCKARKKVQRTDGDPLMVDVVYKGVHSCAGVHSDSQRSSAASSKSNLRPTKSM

QVRASSKDVGPPDDGYSWKRYGQKNIFGANYPRCYYRCIHKTTTGCTATKNAQATDGD

PLLFDVVYHGEHTCDLQSTHSNDVEPIRPQSGLDDDMCTDDTTTVSTRHDSNTDASSI

SFQLDWTNCKDESDGPPTTL</aaseq>

Gene Sequence

<dnaseqindica>

       1 atggaaagaa ggaaggtgat caggatgagt tatacagagg atgacggctt cagctggagg
      61 aagtacgggc agaaggacgt ggaaggcgcc atgcacccaa ctacccaaag taagtaagcg
     121 atgacgactc gtgccaatta acttaaagtt aaattaaggt tgattgattt aatgaagcat
     181 cgaatgcatg caaagagctt aattaattaa gagcagagcg gaataatctg attaacccga
     241 tcttgttcaa cttataactg tcgtcggaac tctactcttg tagaagttat ttccgatgtg
     301 cccacaagat gacgacgggc tgtaaggcac ggaagaaggt gcagcgcacc gacggcgacc
     361 cgctgatggt cgacgtcgta tacaaggggg ttcacagctg tgccggcgtg cattccgaca
     421 gccagagatc atccgccgcg agctctaagt ctaacctgcg gccgacgaag agcatgcagg
     481 tgagggcgag ctccaaggac gtcggccccc cagacgacgg ttacagctgg aagaggtacg
     541 gccagaagaa catcttcggc gctaattacc caaggttagt ggctgattaa cgtacgactg
     601 tacctgaaat gaactggcac tgctgctgga gtacatgaaa tcgaactgat ctcgctcgcc
     661 atctattttg cagatgctac taccggtgta tacacaagac cacgacgggc tgcactgcga
     721 caaaaaatgc acaggccacc gatggtgacc cactcctctt cgacgtcgtg taccacgggg
     781 agcacacctg cgatctgcag agcacgcact ccaacgacgt cgaaccgatc aggccgcagt
     841 ctgggctcga cgacgacatg tgtaccgacg atacgacgac tgtctccaca cgccacgaca
     901 gcaacacgga tgcgtcctca attagttttc aattagattg gaccaattgc aaagacgaat
     961 cggatggccc tcccaccacc ctataa</dnaseqindica>
External Link(s)

NCBI Gene:Os11g0685700, [1]