111 research outputs found

    The accumulation of plutonium isotopes (239+240) in the components of the natural environment in the territory of the Karaganda region adjacent to the Semipalatinsk test site

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    Presents the results of a radiological survey of the territory of the Karaganda region. The data obtained on contamination of isotopes of plutonium (239+240), assessed the impact of nuclear testing on Semipalatinsk testing nuclear polygon. Currently, the pollution of the examined areas of technogenic radionuclides in most places, does not exceed the background level of global fallout, and only at some points noted in the reading background of global fallout. However, there are local areas of contamination, which could be formed as a result of testing of BRV, or other atmospheric fallout from nuclear testing

    Characterization of the rice pathogen-related protein Rir1a and regulation of the corresponding gene

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    In rice (Oryza sativa L.), local acquired resistance against Pyricularia oryzae (Cav.), the causal agent of rice blast, can be induced by a preinoculation with the non-host pathogen Pseudomonas syringae pv. syringae. We have cloned a cDNA (Rir1a) and a closely related gene (Rir1b) corresponding to transcripts that accumulate in leaf tissue upon inoculation with P. syringae pv. syringae. The cDNA encodes a putative 107 amino acid protein, Rir1a, that exhibits a putative signal peptide cleavage site in its hydrophobic N-terminal part and a C-terminal part that is relatively rich in glycine and proline. The Rir1b gene contains a Tourist and a Wanderer miniature transposable element in its single intron and encodes a nearly identical protein. Rir1a is similar in sequence (ca. 35% identical and ca. 60% conservatively changed amino acids) to the putative Wir1 family of proteins that are encoded by pathogen-induced transcripts in wheat. Using antibodies raised against a Rir1a-fusion protein we show that Rir1a is secreted from rice protoplasts transiently expressing a 35S::Rir1a construct and that the protein accumulates in the cell wall compartment of rice leaves upon inoculation with P. syringae pv. syringae. Possible roles of Rir1a in pathogen defense are discusse

    Evidence for Allele-Specific Levels of Enhanced Susceptibility of Wheat mlo Mutants to the Hemibiotrophic Fungal Pathogen Magnaporthe oryzae pv. Triticum

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    Barley mlo mutants are well known for their profound resistance against powdery mildew disease. Recently, mlo mutant plants were generated in hexaploid bread wheat (Triticum aestivum) with the help of transgenic (transcription-activator-like nuclease, TALEN) and non-transgenic (targeted induced local lesions in genomes, TILLING) biotechnological approaches. While full-gene knockouts in the three wheat Mlo (TaMlo) homoeologs, created via TALEN, confer full resistance to the wheat powdery mildew pathogen (Blumeria graminis f.sp. tritici), the currently available TILLING-derived Tamlo missense mutants provide only partial protection against powdery mildew attack. Here, we studied the infection phenotypes of TALEN- and TILLING-derived Tamlo plants to the two hemibiotrophic pathogens Zymoseptoria tritici, causing Septoria leaf blotch in wheat, and Magnaporthe oryzae pv. Triticum (MoT), the causal agent of wheat blast disease. While Tamlo plants showed unaltered outcomes upon challenge with Z. tritici, we found evidence for allele-specific levels of enhanced susceptibility to MoT, with stronger powdery mildew resistance correlated with more invasive growth by the blast pathogen. Surprisingly, unlike barley mlo mutants, young wheat mlo mutant plants do not show undesired pleiotropic phenotypes such as spontaneous callose deposits in leaf mesophyll cells or signs of early leaf senescence. In conclusion, our study provides evidence for allele-specific levels of enhanced susceptibility of Tamlo plants to the hemibiotrophic wheat pathogen MoT

    Π˜Π½Ρ‚Π΅Π³Ρ€Π°Ρ†ΠΈΡ ΠΌΠ°Π»ΠΎΠ³ΠΎ ΠΈΠ½Π½ΠΎΠ²Π°Ρ†ΠΈΠΎΠ½Π½ΠΎΠ³ΠΎ бизнСса Π² систСму особых экономичСских Π·ΠΎΠ½

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    Π’ Ρ€Π°ΠΌΠΊΠ°Ρ… Π΄Π΅ΡΡ‚Π΅Π»ΡŒΠ½ΠΎΡΡ‚ΠΈ ΠΏΠΎ ΡΡ‚ΠΈΠΌΡƒΠ»ΠΈΡ€ΠΎΠ²Π°Π½ΠΈΡŽ ΠΈ Ρ€Π°Π·Π²ΠΈΡ‚ΠΈΡŽ ΠΌΠ°Π»ΠΎΠ³ΠΎ бизнСса Π½Π° протяТСнии ΡƒΠΆΠ΅ довольно Π΄Π»ΠΈΡ‚Π΅Π»ΡŒΠ½ΠΎΠ³ΠΎ Π²Ρ€Π΅ΠΌΠ΅Π½ΠΈ ΠΏΡ€ΠΎΠ²ΠΎΠ΄ΠΈΠ»ΠΈΡΡŒ Ρ€Π°Π·Π½ΠΎΠ³ΠΎ Ρ€ΠΎΠ΄Π° ΠΌΠ΅Ρ€Ρ‹. Однако Π½Π° сСгодняшний дСнь доля ΠΌΠ°Π»ΠΎΠ³ΠΎ ΠΈ срСднСго бизнСса Π½Π΅ ΠΏΡ€Π΅Π²Ρ‹ΡˆΠ°Π΅Ρ‚ 21% Π’Π’ΠŸ. Π’ структурС ΠΌΠ°Π»ΠΎΠ³ΠΎ бизнСса ΠΏΡ€Π΅ΠΎΠ±Π»Π°Π΄Π°ΡŽΡ‚ прСдприятия, занятыС Π² Ρ‚ΠΎΡ€Π³ΠΎΠ²ΠΎΠΉ сфСрС, Π° доля ΠΈΠ½Π½ΠΎΠ²Π°Ρ†ΠΈΠΎΠ½Π½Ρ‹Ρ… прСдприятий Π½ΠΈΡ‡Ρ‚ΠΎΠΆΠ½Π° ΠΌΠ°Π»Π°. ΠŸΡ€ΠΎΠ±Π»Π΅ΠΌΡƒ развития ΠΌΠ°Π»Ρ‹Ρ… ΠΈΠ½Π½ΠΎΠ²Π°Ρ†ΠΈΠΎΠ½Π½Ρ‹Ρ… прСдприятий ΠΈ ΠΏΠΎΠ²Ρ‹ΡˆΠ΅Π½ΠΈΡ ΠΈΡ… экономичСской эффСктивности, Π½Π΅ΠΎΠ±Ρ…ΠΎΠ΄ΠΈΠΌΠΎ Ρ€Π΅ΡˆΠ°Ρ‚ΡŒ ΠΏΡƒΡ‚Π΅ΠΌ ΠΈΠ½Ρ‚Π΅Π³Ρ€Π°Ρ†ΠΈΠΈ Π΄Π°Π½Π½Ρ‹Ρ… прСдприятий с институтом особой экономичСской Π·ΠΎΠ½Ρ‹ Ρ‚Π΅Ρ…Π½ΠΈΠΊΠΎ-внСдрСнчСского Ρ‚ΠΈΠΏΠ°

    Yeast gene KTI13 (alias DPH8) operates in the initiation step of diphthamide synthesis on elongation factor 2

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    In yeast, Elongator-dependent tRNA modifications are regulated by the Kti11β€’Kti13 dimer and hijacked for cell killing by zymocin, a tRNase ribotoxin. Kti11 (alias Dph3) also controls modification of elongation factor 2 (EF2) with diphthamide, the target for lethal ADP-ribosylation by diphtheria toxin (DT). Diphthamide formation on EF2 involves four biosynthetic steps encoded by the DPH1-DPH7 network and an ill-defined KTI13 function. On further examining the latter gene in yeast, we found that kti13Ξ” null-mutants maintain unmodified EF2 able to escape ADP-ribosylation by DT and to survive EF2 inhibition by sordarin, a diphthamide-dependent antifungal. Consistently, mass spectrometry shows kti13Ξ” cells are blocked in proper formation of amino-carboxyl-propyl-EF2, the first diphthamide pathway intermediate. Thus, apart from their common function in tRNA modification, both Kti11/Dph3 and Kti13 share roles in the initiation step of EF2 modification. We suggest an alias KTI13/DPH8 nomenclature indicating dual-functionality analogous to KTI11/DPH3

    A lineage-specific Exo70 is required for receptor kinase–mediated immunity in barley

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    In the evolution of land plants, the plant immune system has experienced expansion in immune receptor and signaling pathways. Lineage-specific expansions have been observed in diverse gene families that are potentially involved in immunity but lack causal association. Here, we show that Rps8-mediated resistance in barley to the pathogen Puccinia striiformis f. sp. tritici (wheat stripe rust) is conferred by a genetic module: Pur1 and Exo70FX12, which are together necessary and sufficient. Pur1 encodes a leucine-rich repeat receptor kinase and is the ortholog of rice Xa21, and Exo70FX12 belongs to the Poales-specific Exo70FX clade. The Exo70FX clade emerged after the divergence of the Bromeliaceae and Poaceae and comprises from 2 to 75 members in sequenced grasses. These results demonstrate the requirement of a lineage-specific Exo70FX12 in Pur1-mediated immunity and suggest that the Exo70FX clade may have evolved a specialized role in receptor kinase signaling
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