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Concept of natural genome reconstruction. Part 4. Integration of extracellular double-stranded DNA fragments into the genome of hematopoietic stem cells and the formation of extrachromosomal intermediates

https://doi.org/10.18699/vjgb-26-18

Abstract

To assess the possibility of integrating extracellular double-stranded DNA fragments into the recipient genome of hematopoietic stem cells, a complex substrate was constructed consisting of the entire M13F-AluI-M13R fragment and its two restrictive derivatives, appearing after hydrolysis with restriction endonucleases EcoRI and HindIII: M13FAluI-EcoRI and M13R-AluI-HindIII. The substrate contained a pBlueScript+ plasmid polylinker sequence, absent in the human genome, which framed the human AluI fragment cloned at the EcoRV site. Human bone marrow cells were treated with the DNA of the constructed complex substrate; taking into account the repair time of pangenomic single-strand breaks, preparations of metaphase plates were obtained. FISH revealed specific fluorescent signals. Simultaneously, DNA isolated from colonies obtained from bone marrow cells treated with a complex substrate was sequenced. Two rounds of sequencing were carried out: whole-genome and selective after targeted hybridization on metal beads. The results obtained indicate that homologous exchange between extrachromosomal and chromosomal DNA is possible. Integration into the genome via the single-strand annealing mechanism, involving microhomologies, is also possible. Intermediates were discovered that suggest the existence of an unusual integration into the genome at the nick of one end of the fragment and the other end of the fragment hanging freely into the interchromosomal space. A direct assessment of the possibility of integrating TAMRA-labeled fragments of fragmented human DNA and E. coli DNA into the genome of recipient cells was carried out using a human bone marrow cell model. The results obtained indicate that specific signals of homologous DNA are distributed throughout the chromosome body (human bone marrow cell model). Signals from nonhomologous E. coli DNA are predominantly concentrated in the centromeric regions of chromosomes. The ratio of the number of obtained reads with integration elements and FISH signals suggested the existence of a strong interaction between extracellular fragments and chromosomal DNA. Experiments have been conducted showing that linear plasmid DNA, after internalization into hematopoietic stem cells, forms a monomer ring. Internalized into the intracellular space, extracellular plasmid DNA is isolated together with chromosomal DNA after stringent purification and fractionation procedures. This fact suggests the existence of a strong ring associate of plasmid DNA and chromosome DNA formed without the participation of a protein framework in the form of a looped chromosomal strand.

About the Authors

S. G. Oshikhmina
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences; Novosibirsk State University
Russian Federation

Novosibirsk



V. S. Ruzanova
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences
Russian Federation

Novosibirsk



G. S. Ritter
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences
Russian Federation

Novosibirsk



E. V. Dolgova
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences
Russian Federation

Novosibirsk



S. S. Kirikovich
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences
Russian Federation

Novosibirsk



E. V. Levites
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences
Russian Federation

Novosibirsk



Y. R. Efremov
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences
Russian Federation

Novosibirsk



T. V. Karamysheva
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences
Russian Federation

Novosibirsk



A. S. Molodtseva
Institute of Molecular and Cellular Biology of the Siberian Branch of the Russian Academy of Sciences
Russian Federation

Novosibirsk



Y. V. Raitsina
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences; Novosibirsk State University
Russian Federation

Novosibirsk



O. S. Taranov
State Scientific Center of Virology and Biotechnology “Vector” of Rospotrebnadzor
Russian Federation

Koltsovo, Novosibirsk region



S. V. Sidorov
Novosibirsk State University; City Clinical Hospital No. 1
Russian Federation

Novosibirsk



S. D. Nikonov
Novosibirsk Tuberculosis Research Institute
Russian Federation

Novosibirsk



O. Y. Leplina
Research Institute of Fundamental and Clinical Immunology
Russian Federation

Novosibirsk



A. A. Ostanin
Research Institute of Fundamental and Clinical Immunology
Russian Federation

Novosibirsk



E. R. Chernykh
Research Institute of Fundamental and Clinical Immunology
Russian Federation

Novosibirsk



N. A. Kolchanov
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences
Russian Federation

Novosibirsk



A. S. Proskurina
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences
Russian Federation

Novosibirsk



S. S. Bogachev
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences
Russian Federation

Novosibirsk



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