Biopolym. Cell. 1995; 11(2):29-38.
Mobile genetics and forms of heritable changes in eukaryotes
1Golubovsky M.
  1. St. Petersburg Branch of the Institute for the History of Science and Technology named after S. I. Vavilov, RAS
    Universitetskaya naberezhnaya, 5., Saint-Petersburg, Russian Federation, 199164

Abstract

The real insight in the eukaryotic genome means knowledge of the structure of genetic elements, the character of dynamic links between them and some holistic features of the system. The structure of the eukaryotic genome can be naturally subdivided on two classes of elements: an obligatory and facultative ones. Accordingly, we need to discriminate between two different forms of heritable changes – mutations and variations. Mutations correspond to all changes with genes. Variations are various kinds of changes in the populations of genomic facultative elements. Variations may be directed and connected with multiple site specific alterations. The spontaneous mutation process in nature is mediated by the system of facultative elements. Their activation in nature induces sudden mutation outbursts, appearance of new genetic constructions and site specific rearrangements. Facultative elements are the first to react on environmental challenge. Variations can be presented as an operational memory of the genome. Between obligatory and facultative elements there is constant flow. The behavior of transposons in the eukaryotic genome may be model for the adequate description of epigenic inheritance. There is logic and real necessity to use the epigene concept for describing of elementary units of epigenetic inheritance.

References

[1] Jacob F, Monod J. Genetic regulatory mechanisms in the synthesis of proteins. J Mol Biol. 1961;3:318-56.
[2] Jacob F, Wollman EL. Sexuality and genetics of bacteria-New York : Acad, press, 1961; 374 p
[3] Golubovsky MD. Organization of the genotype and forms of hereditary variability in eukaryotes. Usp Sovrem Biol. 1985; 100(3(6)):323-39.
[4] Bran G., Plus N. The viruses of Drosophila. The genetics and biology of Drosophila. Eds. M. Ashburner, T. R. Wright. New York : Acid, press, 1980;(2):624-702.
[5] Mobile DNA. Eds D. Berg, M. M. Howe. Washington: Amer. Soc. Microb., 1989.
[6] Kim A, Terzian C, Santamaria P, Pélisson A, Purd'homme N, Bucheton A. Retroviruses in invertebrates: the gypsy retrotransposon is apparently an infectious retrovirus of Drosophila melanogaster. Proc Natl Acad Sci U S A. 1994;91(4):1285-9.
[7] Kidwell MG. Lateral transfer in natural populations of eukaryotes. Annu Rev Genet. 1993;27:235-56.
[8] Reanney D. Genetic noise in evolution? Nature. 1984 Jan 26-Feb 1;307(5949):318-9.
[9] Foster PL. Adaptive mutation: the uses of adversity. Annu Rev Microbiol. 1993;47:467-504.
[10] Berg R, Engels WR, Kreber RA. Site-specific X-chromosome rearrangements from hybrid dysgenesis in Drosophila melanogaster. Science. 1980;210(4468):427-9.
[11] Landman OE. The inheritance of acquired characteristics. Annu Rev Genet. 1991;25:1-20.
[12] McClintock B. The significance of responses of the genome to challenge. Science. 1984;226(4676):792-801.
[13] BERG RL. Mutability changes in Drosophila melanogaster populations of Europe, Asia, and North America and probable mutability changes in human populations of the U.S.S.R.. Jpn J Genet. 1982;57(2):171–83.
[14] Golubovsky MD. Mutational process and microevolution. Genetica. 1984;52-53(1):139–49.
[15] Golubovsky MD, Ivano YN, Green MM. Genetic instability in Drosophila melanogaster: putative multiple insertion mutants at the singed bristle locus. Proc Natl Acad Sci U S A. 1977;74(7):2973-5.
[16] Golubovsky MD, Belayeva ES. Outburst of mutatbility in nature and movable genetic elements: the analysis of multiple singed alleles in Drosophila melanogaster. Genetika. 1985; 21(10):1662-70.
[17] Zakharov IK, Golubovsky MD. Return of the vogue to yellow mutation in the natural population of Drosophila melanogaster in Uman of the Ukrainian SSSR. Genetika. 1985;21(8):1298-305.
[18] Gershenson SM. Viruses as environmental mutagenic factors. Mutat Res. 1986;167(3):203-13.
[19] Alexandrov Yu. N., Golubovsky M. D. The multisite mutations induced by viruses and foreign DNA can spread in natural populations of Drosophila. Drosophila Inf. Serv. 1983; 59: 10-12.
[20] Golubovsky MD, Plus N. Mutability studies in two Drosophila melanogaster isogenic stocks, endemic for C picornavirus and virus-free. Mutat Res. 1982;103(1):29-32.
[21] Yurchenko NN, Zakharov IK, Golubovsky MD. Unstable alleles of the singed locus in Drosophila melanogaster with reference to a transposon marked with a visible mutation. Mol Gen Genet. 1984;194(1-2):279–85.
[22] Shapiro JA. Natural genetic engineering in evolution. Genetica. 1992;86(1-3):99–111.
[23] Plus N, Golubovsky MD. Resistance of Drosophila C virus of fifteen 1 (2) gl. Cy stocks carrying 1 (2) gl lethals from different geographical origin. Genetica. 1980; 12: 227-30.
[24] Green MM, Shepherd SH. Genetic instability in Drosophila melanogaster: the induction of specific chromosome 2 deletions by MR elements. Genetics. 1979;92(3):823-32.
[25] Mechler BM, McGinnis W, Gehring WJ. Molecular cloning of lethal(2)giant larvae, a recessive oncogene of Drosophila melanogaster. EMBO J. 1985;4(6):1551-7.
[26] Monod J, Jacob F. Teleonomic mechanisms in cellular metabolism, growth, and differentiation. Cold Spring Harb Symp Quant Biol. 1961;26:389-401.
[27] Churaev RN. Applied aspects of the concept of epigenes. Zh Obshch Biol. 1982;43(1):79-87.
[28] Holliday R. The inheritance of epigenetic defects. Science. 1987;238(4824):163-70.
[29] Rio DC. Regulation of Drosophila P element transposition. Trends Genet. 1991;7(9):282-7.
[30] Gierl A. How maize transposable elements escape negative selection. Trends Genet. 1990;6(5):155-8.
[31] Fedoroff N, Masson P, Banks JA. Mutations, epimutations, and the developmental programming of the maizeSuppressor-mutator transposable element. BioEssays. 1989;10(5):139–44.
[32] Cline TW. The Drosophila sex determination signal: how do flies count to two? Trends Genet. 1993;9(11):385-90.
[33] Brettell RI, Dennis ES. Reactivation of a silent Ac following tissue culture is associated with heritable alterations in its methylation pattern. Mol Gen Genet. 1991;229(3):365-72.