Vladimir E. Alatortsev
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Vladimir E. Alatortsev has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Alexander V. Symonenko
National Research Centre “Kurchatov Institute”, 2 Kurchatov Sq., 123182 Moscow, Russia
1 shared publication - Anna V. Krementsova
National Research Centre “Kurchatov Institute”, 2 Kurchatov Sq., 123182 Moscow, Russia
1 shared publication - Dmitry V. Mukha
Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia
1 shared publication - Elena A. Mikhaleva
Laboratory of Molecular Genetics of Animals, National Research Centre “Kurchatov Institute”, Moscow 123182, Russia
1 shared publication - Elena G. Pasyukova
National Research Centre “Kurchatov Institute”, 2 Kurchatov Sq., 123182 Moscow, Russia
1 shared publication - Evgeniya A. Tsybul’Ko
National Research Centre “Kurchatov Institute”, 2 Kurchatov Sq., 123182 Moscow, Russia
1 shared publication
Latest Publications
- Open Access
- 19 September 2026
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 27 (18) , 8343
Naturally Occurring Variability in the Regulatory Region of the Drosophila melanogaster Gene shuttle craft Affects Gene Expression and Lifespan
Revealing gene expression patterns is essential for comprehending the genetic control of complex traits like lifespan. Analyzing structural variation in gene regulatory regions within natural populations is a promising approach in functional genetics, allowing us to identify regulatory sites that influence transcription and phenotype in vivo. We describe the structural variability of the 5′ regulatory region of the shuttle craft (stc) gene in the Alexandrov population (Russia) of Drosophila melanogaster, encoding a transcription factor homologous to human NF-X1. We evaluated the association of frequently occurring polymorphisms with fly lifespan from inbred lines sampled in 2010, 2011, and 2014. Two polymorphisms in the stc 5′ regulatory region exhibit strong associations with both lifespan and embryonic stc transcript levels. Their role in expression regulation was evaluated via reporter gene assays conducted in S2 Drosophila cell culture. The ‘C’ allele at one polymorphic site and ‘T’ at the other are associated with increased longevity and decreased embryonic stc transcription, reaffirming the link between gene expression and lifespan we previously established. Furthermore, comparing stc 5′ regulatory region variability across Alexandrov, European and African populations suggests that the macro-geographic distribution of these longevity-associated variants is consistent with a potential role in latitudinal or climatic adaptation.
- 19 September 2026
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 27 (18) , 8343
Open AccessNaturally Occurring Variability in the Regulatory Region of the Drosophila melanogaster Gene shuttle craft Affects Gene Expression and Lifespan
Revealing gene expression patterns is essential for comprehending the genetic control of complex traits like lifespan. Analyzing structural variation in gene regulatory regions within natural populations is a promising approach in functional genetics, allowing us to identify regulatory sites that influence transcription and phenotype in vivo. We describe the structural variability of the 5′ regulatory region of the shuttle craft (stc) gene in the Alexandrov population (Russia) of Drosophila melanogaster, encoding a transcription factor homologous to human NF-X1. We evaluated the association of frequently occurring polymorphisms with fly lifespan from inbred lines sampled in 2010, 2011, and 2014. Two polymorphisms in the stc 5′ regulatory region exhibit strong associations with both lifespan and embryonic stc transcript levels. Their role in expression regulation was evaluated via reporter gene assays conducted in S2 Drosophila cell culture. The ‘C’ allele at one polymorphic site and ‘T’ at the other are associated with increased longevity and decreased embryonic stc transcription, reaffirming the link between gene expression and lifespan we previously established. Furthermore, comparing stc 5′ regulatory region variability across Alexandrov, European and African populations suggests that the macro-geographic distribution of these longevity-associated variants is consistent with a potential role in latitudinal or climatic adaptation.