Chromosomal location and expression of a herbicide safener-regulated glutathione S-transferase gene in Triticum aestivum and linkage relations in Hordeum vulgare

Genome ◽  
1998 ◽  
Vol 41 (3) ◽  
pp. 368-372 ◽  
Author(s):  
Dean E Riechers ◽  
Andris Kleinhofs ◽  
Gerard P Irzyk ◽  
Stephen S Jones
Keyword(s):  
Triticum Aestivum ◽  
Hordeum Vulgare ◽  
Chromosomal Location ◽  
Single Copy ◽  
Rflp Marker ◽  
Glutathione S Transferase ◽  
Triticum Tauschii ◽  
Herbicide Safener ◽  
Mrna Transcripts ◽  
Copy Gene

The chomosomal location of a glutathione S-transferase (GST) gene was determined in both hexaploid wheat (Triticum aestivum) and barley (Hordeum vulgare). The GST cDNA used to map the gene was cloned from the diploid wheat Triticum tauschii. GST loci were located on the short arms of chromosomes 6A, 6B, and 6D in T. aestivum and also on the short arm of chromosome 6H in H. vulgare. The GST locus in barley was absolutely linked to the RFLP marker E148A and was located 0.8 cM proximal to the RFLP marker ABC169B on barley chromosome 6H. At least two copies of the GST gene were present in each of the T. aestivum A, B, and D genomes, and a homologous GST gene was present as a single-copy gene in the barley genome. GST mRNA transcripts were not detected in RNA isolated from shoots of control (unsafened) seedlings of T. tauschii or T. aestivum. It was determined that the expression of the GST gene was regulated by herbicide safener treatment in T. tauschii and T. aestivum by detecting safener-increased GST mRNA transcript levels.Key words: Triticum aestivum, Triticum tauschii, Hordeum vulgare, herbicide safener, glutathione S-transferase, genetic mapping.

Novel chicken actin gene: third cytoplasmic isoform

1985 ◽  
Vol 5 (5) ◽  
pp. 1151-1162
Author(s):  
D J Bergsma ◽  
K S Chang ◽  
R J Schwartz
Keyword(s):  
Nucleotide Sequence ◽  
Single Copy ◽  
Actin Gene ◽  
Single Copy Gene ◽  
Gene Diversification ◽  
Mrna Transcripts ◽  
Copy Gene ◽  
Actin Mrna ◽  
Distinct Member ◽  
Actin Protein

We identified a novel chicken actin gene. The actin protein deduced from its nucleotide sequence very closely resembles the vertebrate cytoplasmic actins; accordingly, we classified this gene as a nonmuscle type. We adopted the convention for indicating the nonmuscle actins of the class Amphibia (Vandekerckhove et al., J. Mol. Biol. 152:413-426) and denoted this gene as type 5. RNA blot analysis demonstrated that the type 5 actin mRNA transcripts accumulate in adult tissues in a pattern indicative of a nonmuscle actin gene. Genomic DNA blots indicated that the type 5 actin is a single copy gene and a distinct member of the chicken actin multigene family. Inspection of the nucleotide sequence revealed many features that distinguished the type 5 gene from all other vertebrate actin genes examined to date. These unique characteristics include: (i) an initiation Met codon preceding an Ala codon, a feature previously known only in plant actins, (ii) a single intron within the 5' untranslated region, with no interruptions in the coding portion of the gene, and (iii) an atypical Goldberg-Hogness box (ATAGAA) preceding the mRNA initiation terminus. These unusual features have interesting implications for actin gene diversification during evolution.

scholarly journals Novel chicken actin gene: third cytoplasmic isoform.

1985 ◽  
Vol 5 (5) ◽  
pp. 1151-1162 ◽  
Author(s):  
D J Bergsma ◽  
K S Chang ◽  
R J Schwartz
Keyword(s):  
Nucleotide Sequence ◽  
Single Copy ◽  
Actin Gene ◽  
Single Copy Gene ◽  
Gene Diversification ◽  
Mrna Transcripts ◽  
Copy Gene ◽  
Actin Mrna ◽  
Distinct Member ◽  
Actin Protein

We identified a novel chicken actin gene. The actin protein deduced from its nucleotide sequence very closely resembles the vertebrate cytoplasmic actins; accordingly, we classified this gene as a nonmuscle type. We adopted the convention for indicating the nonmuscle actins of the class Amphibia (Vandekerckhove et al., J. Mol. Biol. 152:413-426) and denoted this gene as type 5. RNA blot analysis demonstrated that the type 5 actin mRNA transcripts accumulate in adult tissues in a pattern indicative of a nonmuscle actin gene. Genomic DNA blots indicated that the type 5 actin is a single copy gene and a distinct member of the chicken actin multigene family. Inspection of the nucleotide sequence revealed many features that distinguished the type 5 gene from all other vertebrate actin genes examined to date. These unique characteristics include: (i) an initiation Met codon preceding an Ala codon, a feature previously known only in plant actins, (ii) a single intron within the 5' untranslated region, with no interruptions in the coding portion of the gene, and (iii) an atypical Goldberg-Hogness box (ATAGAA) preceding the mRNA initiation terminus. These unusual features have interesting implications for actin gene diversification during evolution.

Effects of tribenuron-methyl treatment on glutathione S-transferase (GST) activities in some wheat and barley varieties

2010 ◽  
Vol 82 (1) ◽  
pp. 289-297 ◽  
Author(s):  
Elif Oztetik
Keyword(s):  
Triticum Aestivum ◽  
Hordeum Vulgare ◽  
Weed Management ◽  
Crop Production ◽  
Environmental Safety ◽  
Glutathione S Transferase ◽  
Maximum Increase ◽  
Treatment Conditions ◽  
Multifunctional Enzymes ◽  
Tribenuron Methyl

For efficient and profitable crop production, appropriate weed management is essential. Today, herbicides are an integral part of modern farming practice globally, as they assure the convenient method of weed control chemically. Glutathione S-transferases (GSTs, EC.2.5.1.18) are a superfamily of multifunctional enzymes that detoxify endo- and xeno-biotic compounds by conjugating glutathione (GSH) to a hydrophobic substrate. Plant GSTs have been a focus of attention because of their roles in herbicide detoxification and environmental safety. In this study, the application of herbicide called tribenuron-methyl to the cultivars of wheat (Triticum aestivum L. cv. Izgi-2001, Triticum aestivum L. cv. Alpu-2001) and barley plants (Hordeum vulgare L. cv. Bilgi-91, Hordeum vulgare L. cv. Kalayci-97) caused an increase in GST activities of both in roots and shoots. Total GSH and protein contents were also determined for all above-mentioned plants. As a conclusion, our results indicate that depending on the herbicide itself, treatment conditions and the origin of the plant, tribenuron-methyl had an effect on the parameters measured in this study, including the GST activities and synthesis of GSH. The maximum increase in enzyme activity was observed in herbicide-treated Triticum aestivum L. cv. Izgi-2001 roots: 192 % of control with a tribenuron-methyl concentration of 1.5 M. However, further investigations are needed to elucidate the presence of specific tribenuron-methyl GST isozymes in this plant.

Ultrastructure of Plant Leaf Tissue Infected with Mite-Borne Viral-Like Pathogens

1970 ◽  
Vol 28 ◽  
pp. 178-179 ◽  
Author(s):  
O. E. Bradfute ◽  
R. E. Whitmoyer ◽  
L. R. Nault
Keyword(s):  
Triticum Aestivum ◽  
Zea Mays ◽  
Electron Microscope ◽  
Hordeum Vulgare ◽  
Microscope Study ◽  
Electron Microscope Study ◽  
Leaf Tissue ◽  
Leaf Ultrastructure ◽  
Double Membrane ◽  
Aceria Tulipae

A pathogen transmitted by the eriophyid mite, Aceria tulipae, infects a number of Gramineae producing symptoms similar to wheat spot mosaic virus (1). An electron microscope study of leaf ultrastructure from systemically infected Zea mays, Hordeum vulgare, and Triticum aestivum showed the presence of ovoid, double membrane bodies (0.1 - 0.2 microns) in the cytoplasm of parenchyma, phloem and epidermis cells (Fig. 1 ).

Identification of a single-copy gene encoding a Type I chlorophyll a/b-binding polypeptide of photosystem I in Arabidopsis thaliana

1992 ◽  
Vol 84 (4) ◽  
pp. 561-567 ◽  
Author(s):  
Poul E. Jensen ◽  
Michael Kristensen ◽  
Tine Hoff ◽  
Jan Lehmbeck ◽  
Bjarne M. Stummann ◽  
...  
Keyword(s):  
Arabidopsis Thaliana ◽  
Chlorophyll A ◽  
Photosystem I ◽  
Single Copy ◽  
Type I ◽  
Single Copy Gene ◽  
Gene Encoding ◽  
Copy Gene

A Mouse Single-Copy Gene,Gtf2i,the Homolog of HumanGTF2I,That Is Duplicated in the Williams–Beuren Syndrome Deletion Region

Genomics ◽  
1998 ◽  
Vol 48 (2) ◽  
pp. 163-170 ◽  
Author(s):  
Yu-Ker Wang ◽  
Luis A. Pérez-Jurado ◽  
Uta Francke
Keyword(s):  
Single Copy ◽  
Single Copy Gene ◽  
Deletion Region ◽  
Copy Gene

scholarly journals Characterization of the Major Antigenic Protein 2 of Ehrlichia canis and Ehrlichia chaffeensis and Its Application for Serodiagnosis of Ehrlichiosis

2003 ◽  
Vol 10 (4) ◽  
pp. 520-524 ◽  
Author(s):  
Tamece T. Knowles ◽  
A. Rick Alleman ◽  
Heather L. Sorenson ◽  
David C. Marciano ◽  
Edward B. Breitschwerdt ◽  
...  
Keyword(s):  
Blot Analysis ◽  
Single Copy ◽  
Ehrlichia Canis ◽  
Specific Method ◽  
Ehrlichia Chaffeensis ◽  
Antigenic Protein ◽  
Canine Monocytic Ehrlichiosis ◽  
Copy Gene ◽  
Species Specific

ABSTRACT Canine monocytic ehrlichiosis, caused by Ehrlichia canis or Ehrlichia chaffeensis, can result in clinical disease in naturally infected animals. Coinfections with these agents may be common in certain areas of endemicity. Currently, a species-specific method for serological diagnosis of monocytic ehrlichiosis is not available. Previously, we developed two indirect enzyme-linked immunosorbent assays (ELISAs) using the major antigenic protein 2 (MAP2) of E. chaffeensis and E. canis. In this study, we further characterized the conservation of MAP2 among various geographic isolates of each organism and determined if the recombinant MAP2 (rMAP2) of E. chaffeensis would cross-react with E. canis-infected dog sera. Genomic Southern blot analysis using digoxigenin-labeled species-specific probes suggested that map2 is a single-copy gene in both Ehrlichia species. Sequences of the single map2 genes of seven geographically different isolates of E. chaffeensis and five isolates of E. canis are highly conserved among the various isolates of each respective ehrlichial species. ELISA and Western blot analysis confirmed that the E. chaffeensis rMAP2 failed to serologically differentiate between E. canis and E. chaffeensis infections.

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