Understanding the molecular mechanisms of plant response to unfavorable conditions is necessary for the effective selection of tolerant genotypes. Earlier, using high-throughput transcriptome sequencing of flax plants after exposure to aluminum ions (Al^(3+)) and high soil acidity, we detected stress-induced alteration in the expression of several genes, including CAX3, which encodes Ca^(2+)/H^(+)-exchanger involved in calcium ion transport. Here we describe CAX3 mRNA levels in flax cultivars either tolerant (Hermes and TMP1919) or sensitive (Lira and Orshanskiy) to Al^(3+). Stress-induced increased expression of CAX3 was detected only in aluminum-tolerant flax cultivars. The product of CAX3 gene may participate in flax response to high soil acidity and high Al^(3+) concentration through Ca^(2+)-mediated intracellular regulation.
Antiporters/genetics , Flax/genetics , Plant Proteins/genetics , Soil/chemistry , Acids/toxicity , Aluminum/toxicity , Flax/drug effects , Flax/growth & development , Gene Expression Regulation, Plant , Genotype , High-Throughput Nucleotide Sequencing , RNA, Messenger/genetics , Stress, Physiological
The appearance of a new scientific term is a significant event in the human cognitive process and the result of the realization of the separateness of an object or a phenomenon. Our article concentrates on the origins of basic genetic terms, such as genetics, gene, genotype, genome, gene pool, and genomics. We propose using the term karyogenomics for the special direction of genomics related to the study of the organization and evolution of eukaryotic genomes by means of modern chromosome analysis, as well as by full genome sequencing.
Regulation of gene expression via microRNA is the key mechanism of response to biotic and abiotic stresses in plants. There are a lot of experimental data on the biological function of microRNAs in response to different stresses in various plant species. This review contains up-to-date information on molecular mechanisms of microRNA action in plants in response to abiotic stresses, including drought, salinity, mineral nutrient deficiency or imbalance.
Arabidopsis/genetics , Gene Expression Regulation, Plant , Medicago truncatula/genetics , MicroRNAs/genetics , Oryza/genetics , RNA, Plant/genetics , Arabidopsis/growth & development , Droughts , Gene Expression Profiling , Medicago truncatula/growth & development , Molecular Sequence Annotation , Oryza/growth & development , Plant Leaves/genetics , Salinity , Stress, Physiological/genetics
Spontaneous transformation of mouse embryonic fibroblasts in the presence of the reverse transcriptase inhibitors azidothymidine and carbovir led to the formation of telomerase-free clones. After prolonged cultivation of fibroblasts in the presence of carbovir, resistant cells with a very high level of telomerase activity were obtained. Azidothymidine and carbovir, but not dideoxycytidine, induced senescence-like processes in cultures of immortal mouse fibroblasts. After long-term incubation, cell proliferation gradually decreased, their morphology becoming similar to that of the senescent ones. The process was reversible: after inhibitor removal, the cells, including the giant ones, entered mitoses. All these data suggest that reverse transcriptase inhibitors block telomerase function in mouse cells.
Cellular Senescence/drug effects , Reverse Transcriptase Inhibitors/pharmacology , Telomerase/antagonists & inhibitors , Zidovudine/pharmacology , 3T3 Cells , Animals , Antiviral Agents/pharmacology , Base Sequence , Cell Division/drug effects , Cell Line, Transformed , Cell Transformation, Viral , Cells, Cultured , Dideoxynucleosides/pharmacology , Dose-Response Relationship, Drug , Drug Resistance , Fibroblasts/drug effects , Fibroblasts/physiology , Fibroblasts/virology , Mice , Mice, Inbred CBA , Mitosis/drug effects , Molecular Sequence Data , Polyploidy , Simian virus 40/genetics , Telomerase/metabolism
Wheat chromosomes of the primary winter hexaploid and octoploid triticales and of the parental durum and common wheat varieties were studied using morphometric analysis. The size of some heterochromatic segments was shown to change in triticale. Telomeric and intercalary C-bands both increased and decreased in size whereas centromeric bands only increased. The size variability of C-bands in triticale B-genome chromosomes decreased in most of the cases and increased only for several specific C-bands. The C-bands of homologous B-genome chromosomes changed in the same direction in both triticale forms. The changes in size of the C-bands found in R-genome chromosomes detected earlier in these triticale forms (Badaeva et al. 1986) were shown to coincide in their pattern with the size changes of C-bands in homeological B-genome chromosomes. Our data are indicative of regular, directed chromosomal changes in the triticale karyotype.
R genome chromosomes were studied in two forms of primary triticales (hexaploid 'TPG-1/1-78' and octoploid 'AD 825') and in their parent rye forms (Secale cereale L. cv. 'Kharkovskaya 60' and 'VSKhI', respectively) using the methods of C-banding and morphometric analysis. The size of some heterochromatic segments was shown to alter in the karyotype of triticale. An increase in size was detected approximately in half of all telomeric C-bands; the size of the other C-bands either decreased or did not change. The frequencies of these alterations were 1â¶1. The variability in the size of telomeric C-bands in rye chromosomes diminished in both triticales studied. The two triticale forms inherited variants of R genome chromosome polymorphism predominantly with the medium size range of telomeric C-bands. The centromeric C-bands in both triticale forms either enlarged or did not alter. Possible mechanisms responsible for the observed pattern of alterations are discussed.
Hexaploid triticales were crossed with common wheats, and the resultant froms were selected for either triticale (AD 213/5-80) or common wheat (lines 381/80, 391/80, 393/80). The cytogenetic analysis showed that all forms differ in their chromosome composition. Triticale AD 213/5-80 and wheat line 381/80 were stable forms with 2n = 6x = 42. Lines 391/80 and 393/80 were cytologically unstable. In triticale AD 213/5-80, a 2R (2D) chromosome substitution was found. Each of the three wheat lines had a chromosome formed by the translocation of the short arm of IR into the long arm of the IB chromosome. In line 381/80, this chromosome seems to be inherited from the 'Kavkaz' wheat variety. In lines 391/80 and 393/80, this chromosome apparently formed de novo since the parent forms did not have it. The karyotype of line 381/80 was found to contain rye chromosomes 4R/7R, 5R and 7R/4R. About 15% of the cells in line 391/80 contained an isochromosome for the 5R short arm and also a chromosome which arose from the translocation of the long arms of the 5D and 5R chromosomes. About one-third of the cells in the common wheat line 393/80 contained the 5R chromosome. This chromosome was normal or rearranged. Practical applications of the C-banding technique in the breeding of triticale is discussed.
