Anna Ivakhnenko
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Anna Ivakhnenko has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Alena Prokofeva
Moscow Center for Advanced Studies, Kulakova Str. 20, 123592 Moscow, Russia
1 shared publication - Alexander Soloviev
All-Russia Research Institute of Agricultural Biotechnology, Timiryazevskaya str. 42, 127550 Moscow, Russia
1 shared publication - Anastasia Vlasova
Moscow Center for Advanced Studies, Kulakova Str. 20, 123592 Moscow, Russia
1 shared publication - Anna Bolotina
Moscow Center for Advanced Studies, Kulakova Str. 20, 123592 Moscow, Russia
1 shared publication - Danil Perevozchikov
Moscow Center for Advanced Studies, Kulakova Str. 20, 123592 Moscow, Russia
1 shared publication - Elizaveta Kamarauli
Moscow Center for Advanced Studies, Kulakova Str. 20, 123592 Moscow, Russia
1 shared publication
Latest Publications
- Open Access
- 26 December 2025
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 27 (1) , 286
Positive-Strand RNA Viruses Induce LTR Retrotransposon Transcription and Extrachromosomal Circular DNA Generation in Plants
Mobile elements, particularly long terminal repeat retrotransposons (LTR-RTEs), are abundant and dynamic components of plant genomes. Although viral infections are known to transcriptionally activate retrotransposons, it remains unclear whether such virus-induced activation leads to their mobilization. To address this question, we examined LTR-RTE activation in Arabidopsis thaliana, Brassica napus, and Nicotiana benthamiana following infection with the RNA viruses Tobacco rattle virus (TRV), Potato virus X (PVX), and Tobacco ringspot virus (TRSV). Nanopore cDNA sequencing revealed virus-specific transcriptional responses, with PVX uniquely triggering a strong transcriptional burst of diverse LTR-RTE families in N. benthamiana. To test the role of viral suppressors of RNA silencing (VSRs) in this process, we analyzed extrachromosomal circular DNA (eccDNA) from plants infected with TRV expressing the VSR P19. This analysis identified eccDNA derived from Ty3/Gypsy Galadriel elements, demonstrating that viral infection can promote not only retrotransposon transcription but also eccDNA production, which may indicate the ability of LTR-RTEs to transpose. These findings clearly illustrate that plant–virus interactions can induce not only changes in gene transcription, but also the activation of multiple retrotransposons, highlighting a potential evolutionary interface linking antiviral defense and transposon regulation.
- 26 December 2025
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 27 (1) , 286
Open AccessPositive-Strand RNA Viruses Induce LTR Retrotransposon Transcription and Extrachromosomal Circular DNA Generation in Plants
Mobile elements, particularly long terminal repeat retrotransposons (LTR-RTEs), are abundant and dynamic components of plant genomes. Although viral infections are known to transcriptionally activate retrotransposons, it remains unclear whether such virus-induced activation leads to their mobilization. To address this question, we examined LTR-RTE activation in Arabidopsis thaliana, Brassica napus, and Nicotiana benthamiana following infection with the RNA viruses Tobacco rattle virus (TRV), Potato virus X (PVX), and Tobacco ringspot virus (TRSV). Nanopore cDNA sequencing revealed virus-specific transcriptional responses, with PVX uniquely triggering a strong transcriptional burst of diverse LTR-RTE families in N. benthamiana. To test the role of viral suppressors of RNA silencing (VSRs) in this process, we analyzed extrachromosomal circular DNA (eccDNA) from plants infected with TRV expressing the VSR P19. This analysis identified eccDNA derived from Ty3/Gypsy Galadriel elements, demonstrating that viral infection can promote not only retrotransposon transcription but also eccDNA production, which may indicate the ability of LTR-RTEs to transpose. These findings clearly illustrate that plant–virus interactions can induce not only changes in gene transcription, but also the activation of multiple retrotransposons, highlighting a potential evolutionary interface linking antiviral defense and transposon regulation.