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1.
BMC Plant Biol ; 10: 168, 2010 Aug 11.
Article in English | MEDLINE | ID: mdl-20699006

ABSTRACT

BACKGROUND: Variability of the VRN1 promoter region of the unique collection of spring polyploid and wild diploid wheat species together with diploid goatgrasses (donor of B and D genomes of polyploid wheats) were investigated. Accessions of wild diploid (T. boeoticum, T. urartu) and tetraploid (T. araraticum, T. timopheevii) species were studied for the first time. RESULTS: Sequence analysis indicated great variability in the region from -62 to -221 nucleotide positions of the VRN1 promoter region. Different indels were found within this region in spring wheats. It was shown that VRN1 promoter region of B and G genome can also contain damages such as the insertion of the transposable element.Some transcription factor recognition sites including hybrid C/G-box for TaFDL2 protein known as the VRN1 gene upregulator were predicted inside the variable region. It was shown that deletions leading to promoter damage occurred in diploid and polyploid species independently. DNA transposon insertions first occurred in polyploid species. At the same time, the duplication of the promoter region was observed in A genomes of polyploid species. CONCLUSIONS: We can conclude that supposed molecular mechanism of the VRN1 gene activating in cultivated diploid wheat species T. monococcum is common also for wild T. boeoticum and was inherited by T. monococcum. The spring polyploids are not related in their origin to spring diploids. The spring T. urartu and goatgrass accessions have another mechanism of flowering activation that is not connected with indels in VRN1 promoter region. All obtained data may be useful for detailed insight into origin of spring wheat forms in evolution and domestication process.


Subject(s)
Genes, Plant/genetics , Genetic Variation , Promoter Regions, Genetic/genetics , Triticum/genetics , Alleles , Base Sequence , Diploidy , Gene Deletion , Molecular Sequence Data , Phylogeny , Polyploidy , Regulatory Elements, Transcriptional/genetics , Seasons , Sequence Alignment , Triticum/classification , Triticum/growth & development , Triticum/metabolism
2.
Cell Biol Int ; 31(2): 97-108, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17085060

ABSTRACT

vasa (vas)-related genes are members of the DEAD-box protein family and are expressed in the germ cells of many Metazoa. We cloned vasa-related genes (PpVLG, CpVLG) and other DEAD-box family related genes (PpDRH1, PpDRH2, CpDRH, AtDRHr) from the colonial parasitic rhizocephalan barnacle Polyascus polygenea, the non-colonial Clistosaccus paguri (Crustacea: Cirripedia: Rhizocephala), and the parasitic isopodan Athelgis takanoshimensis (Crustacea: Isopoda). The colonial Polyascus polygenea, a parasite of the coastal crabs Hemigrapsus sanguineus and Hemigrapsus longitarsis was used as a model object for further detailed investigations. Phylogenetic analysis suggested that PpVLG and CpVLG are closely related to vasa-like genes of other Arthropoda. The rest of the studied genes form their own separate branch on the phylogenetic tree and have a common ancestry with the p68 and PL10 subfamilies. We suppose this group may be a new subfamily of the DEAD-box RNA helicases that is specific for parasitic Crustacea. We found PpVLG and PpDRH1 expression products in stem cells from stolons and buds of internae, during asexual reproduction of colonial P. polygenea, and in germ cells from sexually reproducing externae, including male spermatogenic cells and female oogenic cells.


Subject(s)
DEAD-box RNA Helicases/genetics , Gene Expression Regulation , Parasites/cytology , Parasites/genetics , Stem Cells/metabolism , Thoracica/cytology , Thoracica/genetics , Amino Acid Sequence , Animals , DEAD-box RNA Helicases/chemistry , DEAD-box RNA Helicases/isolation & purification , DEAD-box RNA Helicases/metabolism , Life Cycle Stages , Molecular Sequence Data , Parasites/anatomy & histology , Parasites/growth & development , Phylogeny , RNA, Messenger/genetics , RNA, Messenger/metabolism , Sequence Alignment , Sequence Analysis, DNA , Thoracica/anatomy & histology , Thoracica/growth & development
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