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GrainGenes Sequence Report: NSFT03P2_Contig10316

Sequence
BM138532
Contig
Ta.8544.1.A1_at
NSFT03P2_Contig10316
External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC294163
wEST map position
BM138532
NCBI UniGene
Ta.41066
DB Remark
Locus Source: Triticum aestivum (bread wheat)
UniGene title 'Transcribed locus, moderately similar to NP_001050748.1 Os03g0641700 [Oryza sativa (japonica cultivar-group)]'
Keyword
EST
Species
Triticum aestivum
Cultivar
Sumai3
Chromosome
1BL
1DL
5BL
5DL
Clone Library
Wheat Fusarium graminearum infected spike cDNA library
Tissue
Spike
Developmental Stage
Adult plant
Data Source
genbankRelease 135, Apr 15 2003
genbankUpdated Nov 2006
Title
WHE0492_G09_M18ZS Wheat Fusarium graminearum infected spike cDNA library Triticum aestivum cDNA clone WHE0492_G09_M18, mRNA sequence.
Strain
lab_host E. coli SOLR
Clone
WHE0492_G09_M18
Probe
MAG4165
WHE0492_G09_M18
Remark
DB_xref: taxon:4565
Feature: source: mol_type = 'mRNA';
Locus Comment: Contact: Olin Anderson; US Department of Agriculture, Agriculture Research Service, Pacific; West Area, Western Regional Research Center; 800 Buchanan Street, Albany, CA 94710, USA; Tel: 5105595773; Fax: 5105595818; Email: oandersn@pw.usda.gov; Sequences have been trimmed to remove vector sequence and low; quality sequence with phred score less than 20. No effort was taken; to identify ESTs of fungal origin from this library, thus this EST; could be of wheat or fungal origin.; Seq primer: Stratagene SK primer.
Note: Vector: Lambda Uni-ZAP XR, excised phagemid pBluescript SK; Site_1: EcoRI; Site_2: XhoI; Plants were grown in the greenhouse. Spikes were sprayed at anthesis with Fusarium graminearum. Total RNA, and poly(A) RNA were prepared and pooled from infected spike at 0, 6, 12, 24, 36 and 48 hours after inoculation, a cDNA library was made , and the cDNA clones were in vivo excised to give pBluescript phagemids in G. Muehlbauer lab at the University of Minnesota (Kruger, W.M., Muehlbauer, G.J., Pritsch, C., Vance, C.). The cDNA library should contain genes of both wheat and fungal pathogen origin. Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors).
Note: Vector: Lambda Uni-ZAP XR, excised phagemid pBluescript SK; Site_1: EcoRI; Site_2: XhoI; Plants were grown in the greenhouse. Spikes were sprayed at anthesis with Fusarium graminearum. Total RNA, and poly(A) RNA were prepared and pooled from infected spike at 0, 6, 12, 24, 36 and 48 hours after inoculation, a cDNA library was made, and the cDNA clones were in vivo excised to give pBluescript phagemids in G. Muehlbauer lab at the University of Minnesota (Kruger, W.M., Muehlbauer, G.J., Pritsch, C., Vance, C.). The cDNA library should contain genes of both wheat and fungal pathogen origin. Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors).
DNA Homology
Ta.8544.1.A1_at848WHE2AFFY
Ta.8544.1.A1_at624WHE2AFFY
TaAffx.71479.1.S1_at505WHE2AFFY
TaAffx.71479.1.S1_at68WHE2AFFY
TaAffx.71479.1.S1_at319WHE2AFFY
DNA
caaagagaaagagaaggagaaagagaaagagaaagagaaagagaaagaga
aagagaaagagaaggagaaagacaaagacaaagaaaagaaaaaagagaag
agtgtgcatcatgatttgggaggtgataattccaaaaaacatcatgagaa
gaagaggaaacatgaaggaatggaaaatttggcggctggacgtaaccaca
aaaaaacacaaaagcgcaaagttcaatgaaacgggcaatggactttgttt
ggcataggatgtgacaaattcgtttccgtgttagttctcgtaatatgact
ccatgttttatgctgttaatgggcggctctgaaggttttcttgtcaatac
cacttccgatggagttaccacagatggaatttccttttatcaagatgccc
cggttacaagggacgtggctaatcaaatcacgatacgctgtaaatcaatt
ctgggggaacttgaacttgtcatatggaattatttgaatttttgtgttag
ttttgcgcccattagcaattctttagtgttgccccctcctatatgcccta
tcc

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