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GrainGenes Sequence Report: BI954579

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Sequence
BI954579
External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC188883
DB Remark
Locus Source: Hordeum vulgare subsp. vulgare
Keyword
EST
Species
Hordeum vulgare subsp. vulgare
Cultivar
Morex
Clone Library
Hordeum vulgare green seedling EST library HVcDNA0014 (Blumeria infected)
Tissue
green seedling leaf
Data Source
genbankRelease 135, Apr 15 2003
genbankUpdated Nov 2006
Title
HVSMEm0018L11f Hordeum vulgare green seedling EST library HVcDNA0014 (Blumeria infected) Hordeum vulgare subsp. vulgare cDNA clone HVSMEm0018L11f, mRNA sequence.
Strain
lab_host TJC121
vulgare
Clone
HVSMEm0018L11f
Probe
UMB009
Remark
DB_xref: taxon:112509
Feature: source: mol_type = 'mRNA';
Locus Comment: Contact: Wing RA; Clemson University Genomics Institute; Clemson University; 100 Jordan Hall, Clemson, SC 29634, USA; Tel: 864 656 7288; Fax: 864 656 4293; Email: rwing@clemson.edu; Total hq bases = 485; Seq primer: AATTAACCCTCACTAAAGGG; High quality sequence stop: 550.
Note: Vector: pBluescript SK(-); Site_1: EcoRI; Site_2: XhoI; Morex (mla) plants were greenhouse grown in the R Wise lab at Iowa State University, Ames, IA; 7 day old green seedlings were infected with isolate 5874 of Blumeria graminis f. sp. hordei, and leaves were harvested 24, 48 and 72 hr post-inoculation and snap frozen (Wise). In the TJ Close lab at the University of California, Riverside, total RNA was prepared from each sample pool, equal quantities of all three RNA pools were combined, poly(A) RNA was purified from the mixture, one primary unamplified cDNA library was made, and 1 million pfu were in vivo excised to give pBluescript SK(-) cDNA phagemids (Chin). Phagemids were plated and picked at the Clemson University Genomics Institute (CUGI) (Begum, Palmer, Frisch, Atkins and Wing). Plasmid DNA preparations, DNA sequencing and sequence analysis were performed at CUGI (Wing, Yu, Frisch, Henry, Simmons, Oates, Rambo, Main). The sequence has been trimmed to remove vector sequence and contains a minimum of 100 bases of phred value 20 or above. For more details on library preparation and sequence analysis see http:
DNA
cccatccccatccccatccagatccagccgtcgatgctgcagccccagcc
cacccgcatcgagctccgcagctccgaacgcgacgagatcgaggagcacc
tccgctccaaagccgccgccgccgccgccgccgccgccgaatcctcgcac
ctctcgaccccgccgacgtccaaccccatccccaacccgctcctccgcat
cctccacccgcacgccgacgccgcgcccaccaaggcccagcgcatcggcc
tccaccccccgccccccaaaccctagccccatggaggtcgaggtcaagct
ccgcctccccgacgcggccgcgcaccgccgcctctccgcctacctcgcgc
ctcgcctcctgcgcaccgacgcccagcgcaacgccttcttcgacgccccg
gcccggcccctcgccgccgccaccgccgcgctccgcgtccgcctctacgg
ccccgacgaccgcgctccctcccgcgccgtcctcgcgctcaagcgccgac
cgcgcatgcacgccggcgtcagccgcgtcaaggaggtcnaggagccgctc
gaaccggacctcgcccttncctgcgtcgacgacgcngccggtctgggcgc
gcccgactcacgctngacgagctcgtcgcagaggagtgcggcgcgagggg
g

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