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Vitaly Citovsky

· Professor, Dept. of Biochemistry & Cell BiologyVerified

Stony Brook University · Biology

Active 1985–2026

h-index98
Citations29.4k
Papers34125 last 5y
Funding$9.7M
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About

Vitaly Citovsky is a SUNY Distinguished Professor in the Department of Biochemistry and Cell Biology at Stony Brook University. His research focuses on three main projects: the genetic transformation of plant cells by Agrobacterium, the intercellular transport of plant viruses and plant cell proteins, and the remodeling of plant chromatin by histone modifications. His work with Agrobacterium involves identifying and characterizing cellular systems such as nuclear import machinery, proteolysis machinery, and DNA repair mechanisms that are involved in the nuclear transport and integration of T-DNA, as well as studying bacterial effectors that interact with these plant systems to subvert host defenses. He has demonstrated that this plant pathogen can genetically transform human cells, highlighting the evolutionarily conserved nature of these processes. In the area of plant intercellular transport, Citovsky's research has uncovered mechanisms by which viral genomes move between cells via subviral complexes and the cellular proteins that regulate this process, particularly focusing on plasmodesmata and callose sphincters. His chromatin remodeling studies aim to elucidate the structure, composition, and function of plant corepressor complexes involved in histone modifications, which regulate gene expression during plant development and morphogenesis. Throughout his career, Citovsky has contributed significantly to understanding the molecular interactions involved in plant-pathogen interactions, gene transfer, and gene regulation, with numerous publications and patents to his name.

Research topics

  • Biology
  • Genetics
  • Computer Science
  • Cell biology
  • Computational biology
  • Virology

Selected publications

  • Attenuation of cell-cell movement of tobamoviruses by the C-terminal GPI signal peptide of arabinogalactan protein FLA8

    Current Biology · 2026-04-21

    articleSenior author
  • PDLP5, a plasmodesmata permeability regulator, can traffic between plant cells

    npj Science of Plants · 2025-07-01 · 1 citations

    articleOpen accessSenior author
  • Bioimaging of Element Abundance and Distribution in Response to Boron Availability Extremes

    2025-01-01

    articleOpen accessSenior author
  • The roles of movement and coat proteins in the transport of tobamoviruses between plant cells

    Frontiers in Plant Science · 2025-04-17 · 5 citations

    reviewOpen accessSenior author

    species has been on the rise in recent years, and currently, this genus includes 47 viruses. Tobamoviruses are transmitted mainly by mechanical contact, such as physical touching by hands or agricultural tools; and some are also transmitted on seeds, or through pollinator insects. The tobamoviral genome encodes proteins that have evolved to fulfill the main conceptual task of the viral infection cycle - the spread of the invading virus throughout the host plant cells, tissues, and organs. Here, we discuss this aspect of the infection cycle of tobamoviruses, focusing on the advances in our understanding of the local, i.e., cell-to-cell, and systemic, i.e., organ-to-organ, virus movement, and the viral and host plant determinants of these processes. Specifically, we spotlight two viral proteins-the movement protein (MP) and the coat protein (CP), which are directly involved in the local and systemic spread of tobamoviruses-with respect to their phylogeny, activities during viral movement, and interactions with the host determinants of the movement process.

  • Rhizobium tropici biopolymer enhances lateral root formation in agar-grown Arabidopsis

    Biochemical and Biophysical Research Communications · 2025-05-29 · 1 citations

    articleCorresponding
  • Crown Galls Tumors

    Elsevier eBooks · 2024-01-01

    book-chapterSenior author
  • Agrobacterium virulence factors induce the expression of host DNA repair-related genes without promoting major genomic damage

    Scientific Reports · 2024-10-17 · 3 citations

    articleOpen accessSenior author

    This study aimed to investigate whether the plant DNA damage levels and DNA damage response (DDR) are regulated during Agrobacterium infection and potentially manipulated by Agrobacterium to facilitate T-DNA integration. We investigated the plant genomic response to Agrobacterium infection by measuring gamma H2AX levels, which reflect the levels of double-strand DNA breaks (DSBs), and by characterizing transcription of three major DNA repair marker genes NAC82, KU70, and AGO2. These experiments revealed that, globally, Agrobacterium infection did not result in a major increase in DSB content in the host genome. The transcription of the DNA damage repair genes, on the other hand, was elevated upon the wild-type Agrobacterium infection. This transcriptional outcome was largely negated by a mutation in the bacterial virB5 gene which encodes the virulence (Vir) protein B5, a minor component of Agrobacterium pilus necessary for the translocation of Vir effector proteins into the host cell, suggesting that the transcriptional activation of the cellular DNA damage repair machinery requires the transport into the host cell of the Agrobacterium effectors, i.e., the VirD2, VirD5, VirE2, VirE3, and VirF proteins. Most likely, a combination of several of these Vir effectors is required to activate the host DNA repair as their individual loss- or gain-of-function mutants did not significantly affect this process.

  • Confocal Microscopy Analysis of Protein Sorting to Plasmodesmata in <i>Nicotiana benthamiana</i>

    Journal of Visualized Experiments · 2024-11-01

    articleOpen accessSenior author

    Plasmodesmata are membranous nanopores that connect the cytoplasm of adjacent plant cells and enable the cell-to-cell trafficking of nutrients, macromolecules, as well as invading viruses. Plasmodesmata play fundamental roles in the regulation of intercellular communication, contributing to plant development, environmental responses, and interactions with viral pathogens. Discovering plasmodesmal localization of plant or viral proteins could provide useful functional information about the protein and is important for understanding the mechanisms of plant-virus interactions. To facilitate these studies, we describe a protocol for confocal microscopy-based analysis of different plasmodesmal targeting proteins to select the best plasmodesmal marker for studying the virus-plasmodesmata interactions or plasmodesmal transport. Specifically, the analyses of these events are illustrated using the cell-to-cell movement protein (MP) of the Turnip vein-clearing virus (TVCV), the Arabidopsis Plasmodesmata-Localized Protein 5 (PDLP5) and Plasmodesmata Callose-Binding Protein 1 (PDCB1). The protein plasmodesmal localization data are analyzed in parallel with the global visualization of plasmodesmata using aniline blue staining of the sampled tissues. These approaches can be easily adapted to analyze the plasmodesmal localization of any cellular or pathogen proteins in planta.

  • Faculty Opinions recommendation of Facilitation of symplastic effector protein mobility by paired effectors is conserved in different classes of fungal pathogens.

    Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · 2023-11-28

    dataset1st authorCorresponding
  • Faculty Opinions recommendation of Precise integration of large DNA sequences in plant genomes using PrimeRoot editors.

    Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · 2023-06-29

    dataset1st authorCorresponding

Recent grants

Frequent coauthors

  • Benoît Lacroix

    Stony Brook University

    352 shared
  • Alexander Krichevsky

    111 shared
  • Shimpei Magori

    Stony Brook University

    101 shared
  • Tzvi Tzfira

    Ben-Gurion University of the Negev

    96 shared
  • Renhong Wu

    Southwest University

    94 shared
  • Shoko Ueki

    80 shared
  • Ido Keren

    Stony Brook University

    69 shared
  • Phu‐Tri Tran

    Flagship Pioneering (United States)

    64 shared
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