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1.
Genes (Basel) ; 10(5)2019 05 01.
Article in English | MEDLINE | ID: mdl-31052454

ABSTRACT

Identification and characterization of protein complexes and interactomes has been essential to the understanding of fundamental nuclear processes including transcription, replication, recombination, and maintenance of genome stability. Despite significant progress in elucidation of nuclear proteomes and interactomes of organisms such as yeast and mammalian systems, progress in other models has lagged. Protists, including the alveolate ciliate protozoa with Tetrahymena thermophila as one of the most studied members of this group, have a unique nuclear biology, and nuclear dimorphism, with structurally and functionally distinct nuclei in a common cytoplasm. These features have been important in providing important insights about numerous fundamental nuclear processes. Here, we review the proteomic approaches that were historically used as well as those currently employed to take advantage of the unique biology of the ciliates, focusing on Tetrahymena, to address important questions and better understand nuclear processes including chromatin biology of eukaryotes.


Subject(s)
Ciliophora Infections/genetics , Nuclear Proteins/genetics , Proteomics , Tetrahymena thermophila/genetics , Cell Nucleus/genetics , Cell Nucleus/parasitology , Chromatin/genetics , Chromatin/parasitology , Ciliophora Infections/parasitology , Cytoplasm/genetics , Cytoplasm/parasitology , Humans , Tetrahymena thermophila/pathogenicity
2.
Cell Rep ; 16(6): 1774-1786, 2016 08 09.
Article in English | MEDLINE | ID: mdl-27477279

ABSTRACT

Faithful inheritance of eukaryotic genomes requires the orchestrated activation of multiple DNA replication origins (ORIs). Although origin firing is mechanistically conserved, how origins are specified and selected for activation varies across different model systems. Here, we provide a complete analysis of the nucleosomal landscape and replication program of the human parasite Leishmania major, building on a better evolutionary understanding of replication organization in Eukarya. We found that active transcription is a driving force for the nucleosomal organization of the L. major genome and that both the spatial and the temporal program of DNA replication can be explained as associated to RNA polymerase kinetics. This simple scenario likely provides flexibility and robustness to deal with the environmental changes that impose alterations in the genetic programs during parasitic life cycle stages. Our findings also suggest that coupling replication initiation to transcription elongation could be an ancient solution used by eukaryotic cells for origin maintenance.


Subject(s)
Chromatin/parasitology , DNA Replication/genetics , DNA/metabolism , Leishmania major/genetics , Animals , DNA Replication Timing/genetics , Eukaryotic Cells/parasitology , Humans , Nucleosomes/parasitology , Parasites/genetics , Replication Origin/genetics , Transcription, Genetic
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