English Українська
  • Main
  • Useful links
  • Information for Contributors
  • About
  • Editorial board

  • Article
    V.M. Pomohaibo, O.I. Berezan, M.Y. Delva, A.V. Petrushov

    PROBLEMS OF HORIZONTAL GENE TRANSFER IN HUMAN GENOME


    About the author: V.M. Pomohaibo, O.I. Berezan, M.Y. Delva, A.V. Petrushov
    Heading LITERATURE REVIEWS
    Type of article Review article
    Annotation The overview of publications concerning possibility of a transfer to human genome of genes of other organisms is provided. The horizontal gene transfer (HGT) is rather widespread in the nature, especially among prokaryotes as the tool of adaptive variability. Researchers are interested the HGT presence, prevalence and ability with a man in three directions – phylogenetic, medical and ecological. The phylogenetic approach involves consideration of the HGT phenomenon to interpret a mechanism of human origin and evolution. Already initial sequence data of the human genome sequencing found in it 223 bacterial genes that were probably acquired during evolution of vertebrates. This fact is of interested because the human body is almost same microbial cells as its own. The first direct experimental confirmation of horizontal gene transfer in the human genome that is genome of vertebrates was received by Brazilian researcher group of Professor Antonio Teixeira in 2010 as a result of many years study of Chagas disease patients, which were caused by the unicellular parasite Trypanosoma cruzi. In the genome of healthy individuals whose ancestors were ill with Chagas disease, the researchers found Trypanosoma genes that were passed on to next generations. HGT was realized mainly by means of the LINE-1 transposons in almost all human chromosomes. Greatest number of foreign DNA insertions was found in chromosomes X, 1 and 7. The medical approach is care for HGT using to devise gene therapy technology to treatment various hereditary diseases, mainly cancer. Currently there are only attempts to transfer normal genes in somatic cancer cells by means of diverse vectors (viruses, bacterial plasmids and mobile genetic elements) or as DNA fragments with a wanted gene. A normal gene is not yet possible to integrate into the patient genome and it functions as copies. The gene copy number in cells decreases over time as a result of cell division. As a result the treatment procedure will need to be repeated periodically. In addition, there are other problems of gene therapy: the low level of gene construct transfer into target cells, low levels of introduced gene expression, immune reactions to the vector protein, local and systemic inflammatory processes. The ecological approach involves determining the degree of possible danger to human health to take food products of genetically modified organisms (GMO) and unpredictable consequences of the undesirable genes transfer from these organisms into wild nature. Studies have shown that the risk of GMO foods is much exaggerated. This is confirmed by the statistical data on a normal health and an increase of population in countries where more 15 years GMO products massively are applied, for example the United States and Canada.
    Tags horizontal gene transfer, human genome, gene therapy, genetically modified organisms
    Bibliography
    • Pomohaibo V.M. Henetychni komunikatsii v systemi «parazyt-zhyvytel» / V.M. Pomohaibo, A.V. Petrushov // Svit medytsyny ta biolohii. – 2015. – No.3(51). – S. 142-149.
    • An introduction to molecular medicine and gene therapy (Ed. Th.F. Kresina). – N.Y.: Wiley-Liss, Inc., - 2001. – 386 p.
    • Axelrod J.H. Sixth meeting of the European working group on human gene transfer and therapy (EWGT). Jerusalem, November 21-24, 1998 / J.H. Axelrod // J Gene Med. – 1999. – Vol. 1. – No. 1. – P. 74-76.
    • Boer J.G. Bursts and horizontal evolution of DNA transposons in the speciation of pseudotetraploid salmonids / Johan G de Boer, R. Yazawa, W.S. Davidson and B.F. Koop // BMC Genomics. – 2007. – Vol. 8. – No. 1. – P. 422-431.
    • Doolittle W.F. Phylogenetic classification and the universal tree / W.F. Doolittle // Science. – 1999. – Vol. 284. – No. 5423. – P. 2124-2129.
    • Eede G., van den. The relevance of gene transfer to the safety of food and feed derived from genetically modified (GM) plants / G. van den Eede, H. Aarts, H.-J. Buhk et al. // Food Chem. Toxicol. – 2004. – Vol. 42. – No. 7. – P. 1127-1156.
    • Gene correction: methods and protocols (Ed. F. Storici). – N.Y.: Humana Press, -n2014. – XVI+464 p.
    • Hale M.C. Discovery and evaluation of candidate sex-determining genes and xenobiotics in the gonads of lake sturgeon (Acipenser fulvescens) / M.C. Hale, J.R. Jackson, J.A. DeWoody // Genetica. – 2010. – Vol. 138. – No. 7. – P.  45-756.
    • Hecht M.M. Inheritance of DNA transferred from american trypanosomes to human hosts / M.M. Hecht, N. Nitz, P.F. Araujo et al. // PLoS ONE. – 2010. – Vol. 5. – Iss. 2. – 15 p.
    • Huerta-Cepas J. The human phylome / J. Huerta-Cepas, H. Dopazo, J. Dopazo, T. Gabaldón // Genome Biology. – 2007. – Vol. 8. – No. 6. – R109. – 16 p.
    • Initial sequencing and analysis of the human genome / International Human Genome Sequencing Consortium // Nature. – 2001. – Vol. 409. – No. 6822. – P. 860-921.
    • Jonas D.A.. Safety considerations of DNA in food / D.A. Jonas, I. Elmadfa, K.-H. Engel [et al.] // Ann. Nutr. Metab. – 2001. – Vol. 45. – No. 6. – P. 235-254.
    • Kurland Ch. G. What tangled web: barriers to rampant horizontal gene transfer / Ch. G. Kurland // BioEssays. – 2005. – Vol. 27. – No. 7. – P. 741-747.
    • Kaufmann K. B. Gene therapy on the move / K.B. Kaufmann, H. Büning, A. Galy [et al.] // EMBO Mol. Med. – 2013. – Vol. 5. – No. 11. – P. 1642-1661.
    • Mathiowitz E. Biologically erodable microspheres as potential oral drug delivery system / E. Mathiowitz, J.S. Jacob, Y.S. Jong [et al.] // Nature. – 1997. – Vol. 386. – No. 6623. – P. 410-414.
    • Misra S. Human gene therapy: a brief overview of the genetic revolution / S. Misra // J. Assoc Phys. India. – 2013. – Vol. 61. – No. 2. – P. 41-47.
    • Notzon F.C. Vital and health statistics: Russian Federation and United States, selected years 1985–2000 with an overview of Russian mortality in the 1990s / F.C. Notzon, Y.M. Komarov, S.P. Ermakov [et al.] // Vital Health Statistics. – 2003. – Ser. 5. – No. 11. – P. 15-46.
    • Non-viral gene therapy: Gene design and delivery (Ed. K. Taira, K. Kataoka and T. Niidome). – Japan: Springer-Verlag Tokyo, - 2005. – 488 p.
    • Population, health and environment data and estimates for the countries and regions of the World / In: World Population Data Sheet. – Washington: Population Reference Bureau. – 2015. – P. 11-20.
    • Robinson C.J. From structure to function: the ecology of host-associated microbial communities / C.J. Robinson, B.J.M. Bohannan and V.B. Young // Microbiol. Mol. Biol. Rev. – 2010. – Vol. 74. – No. 3. – P. 453-476.
    • Savage D.C. Microbial ecology of the gastrointestinal tract / D.C. Savage // Annu. Rev. Microbiol. – 1977. – Vol. 31. – No. 1. – P. 107-133.
    • Schubbert R. Ingested foreign (phage M13) DNA survives transiently in the gastrointestinal tract and enters the bloodstream of mice / R. Schubbert, C. Lettmann, W. Doerfler // Mol. Gen. Genet. – 1994. – Vol. 242. – No. 5. – P. 495-504.
    • Schubbert R. Foreign (M13) DNA ingested by mice reaches peripheral leukocytes, spleen, and liver via the intestinal wall mucosa and can be covalently linked to mouse DNA / R. Schubert, D. Renz, B. Schmitz [et al.] // Proc. Natl. Acad. Sci. USA. – 1997. – Vol. 94. – No. 3. – P. 961-966.
    • Schubbert R. On the fate of orally ingested foreign DNA in mice: chromosomal association and placental transmission to the fetus / R. Schubbert, U. Hohlweg, D. Renz [et al.] // Mol. Gen. Genet. – 1998. – Vol. 259. – No. 6. – P. 569-576.
    • Salzberg S.L. Microbial genes in the human genome: lateral transfer or gene loss? / S.L. Salzberg, O. White, J. Peterson, J.A. Eisen // Science. – 2001. – Vol. 292. – No. 5523. – P. 1903-1906.
    • Teixeira A.R. Insertion of Trypanosoma cruzi DNA in the genome of mammal host cell through infection / A.R. Teixeira, Z. Lacava, J.M. Santana [et al.] // Rev. Soc. Bras. Med. Trop. – 1991. – Vol. 24. – No. 1. – P. 55-58.
    • Teixeira A.R. Possible integration of Trypanosoma cruzi kDNA minicircles into the host cell genome by infection / A.R.L. Teixeira, E.R. Argafiaraz, L.H. Freitas Jr. [et al.] // Mutat. Res. – 1994. – Vol. 305. – No. 2. – Р. 197–209.
    • Teixeira A.R. Evolution and pathology in Chagas disease: a review / A.R. Teixeira, R. Nascimento, N.R. Sturm // Mem. Inst. Oswaldo Cruz. – 2006. – Vol. 101. – No. 5. – P. 463-491.
    • Uh M. Transgene constructs in coho salmon (Oncorhynchus kisutch) are repeated in a head-to-tail fashion and can be integrated adjacent to horizontally-transmitted parasite DNA / M. Uh, J. Khattra, R.H. Devlin // Transgenic Res. – 2006. – Vol. 15. – No. 6. – P. 711-727.
    • Volpers Ch. Adenoviral vectors for gene transfer and therapy / Ch. Volpers, S. Kochanek // J. Gene Med. – 2004. – Vol. 6. – No. S1. – P. S164-S171.
    • Willerslev E. Contamination in the draft of the human genome masquerades as lateral gene transfer / E. Willerslev, T. Mourier, A.J. Hansen [et al.] // DNA Sequence. – 2002. – Vol. 13. – No. 2. – P. 75-76.
    • Young J.L. Nonviral gene transfer strategies for the vasculature / J.L. Young, D.A. Dean // Microcirculation. – 2002. – No. 9. – P.35–50.
    Publication of the article «World of Medicine and Biology» №2(60), 2017 year, 190-194 pages, index UDK 575.113