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Khrustaleva, A. M.

Publications and source records attributed to Khrustaleva, A. M..

3 recordsLinked to original sources

Linking Ancient Refugia to Modern Diversity: Evidence of Multi-origin Postglacial Expansion of Sockeye Salmon on the Asian Range

Sockeye salmon (Oncorhynchus nerka) is a traditional object of fishery in the northern Pacific, but its island populations now face emerging threats from territories development and escalating risks of unregulated fishing. The present study aims to assess the current status of Kuril island populations associated with the biogeographical processes in the past. We analyzed diversity distribution of the D-loop sequence and three mtSNPs localized in the Cytb and COI genes in sockeye salmon populations across the North Pacific. mtDNA variants were grouped into two distinct lineages: haplogroups 10T and 13T. Their distribution suggests an Asian origin for the 10T lineage and a North American origin for the 13T haplogroup. Testing the biogeographical scenarios support recurrent postglacial expansions of North American strains into the southernmost territories of the Asian range during the last two glacial cycles. Concurrently, during the Holocene transgression, there were two centers of sockeye salmon radiation in Asia associated with the refugium in the Kamchatka River basin and a minor cryptic refugium in the Hokkaido region. We also propose an island bridge hypothesis to explain dispersal of 10T-lineage from the Kamchatka River basin into Cook Inlet and Alaska Peninsula watersheds via the Aleutian Islands.

genetics↗

Genetic Structuring and Conservation of Asian Sockeye Salmon: Identification of Regional Stock Complexes

In order to describe large-scale spatial structure of Asian sockeye salmon the variability of 45 SNP loci was analyzed in 22 samples from the North-West coast of the Pacific Ocean. Three large regional population complexes were identified: southwestern Kamchatka, Kamchatka River basin, and the North-East (comprising stocks from Koryak Highlands). Populations within the identified complexes are connected by gene migration and have a common origin, close geographic proximity, comparable climatic, landscape and environmental conditions in the freshwater and early marine periods of life. Populations confined to watersheds of the North coast of the Sea of Okhotsk (Palana and Okhota rivers), along with island populations, displayed noteworthy distinctions from the isolated population complexes. We hypothesize that the marked divergence observed in island populations is primarily caused by genetic drift occurring during long periods of isolation. The pronounced divergence of Palana River population may be the result of both genetic drift and natural selection, driven by the challenging smoltification and juvenile transition to the ocean, along with local adaptations during spawning and early life periods in the Palansky Lake. At the same time in the Okhota River population, demographic factors such as genetic drift and bottlenecks played a key role.

genetics↗

CDK8/19 Inhibition Attenuates G1 Arrest Induced by BCR-ABL Antagonists and Accelerates Death of Chronic Myelogenous Leukemia Cells

Imatinib mesylate (IM) and other BCR-ABL tyrosine kinase inhibitors (BCR-ABLi) are the mainstay of chronic myelogenous leukemia (CML) treatment. However, activation of circumventing signaling pathways and quiescence may limit BCR-ABLi efficacy. CDK8/19 Mediator kinases have been implicated in the emergence of non-genetic drug resistance. Dissecting the effects of pharmacological CDK8/19 inhibition on CML survival in response to BCR-ABLi, we found that a selective, non-toxic CDK8/19 inhibitor (CDK8/19i) Senexin B (SenB) and other CDK8/19i sensitized K562 cells to different BCR-ABLi via attenuation of cell cycle arrest. In particular, SenB prevented IM-induced upregulation of genes that negatively regulate cell cycle progression. SenB also antagonized IM-activated p27Kip1 elevation thereby diminishing the population of G1-arrested cells. After transient G1 arrest, cells treated with IM+SenB re-entered the S phase, where they were halted and underwent replicative stress. Consequently, the combination of IM and SenB intensified apoptotic cell death, measured by activation of caspase 9 and 3, subsequent cleavage of poly(ADPriboso)polymerase 1, positive Annexin V staining and increase of subG1 fraction. In contrast, IM-treated BCR-ABL-positive KU812 CML cells, which did not induce p27Kip1, readily died regardless of SenB treatment. Thus, CDK8/19i prevent the quiescence-mediated escape from BCR-ABLi-induced apoptosis, suggesting a strategy for avoiding the CML relapse.

cancer biology↗