Summary
A number of seemingly unrelated phenomena, including high mutability, chromosome breakage, temperature-sensitive sterility, and male crossing-over, appear in certain inter-strain crosses in Drosophila melanogaster. The collection of symptoms has been called “hybrid dysgenesis”. The explanation is a 2907 bp transposable element, designated P. The P element is highly mobile in an appropriate maternally-derived cellular environment, designated M, but hardly at all otherwise. The various manifestations of hybrid dysgenesis are thought to be consequences of P factor transposition.
A complete P factor has 31-base reverse repeat at each end and two internal protein-coding sequences. Incomplete P factors having the repeated ends but lacking the coding regions are transposable, but onyl when at least one complete P factor is present in the nucleus. A specific, extremely highly mutable state of the singed bristle locus is thought to be due to the insertion of one or more incomplete P factors. Mutability at this locus has been employed as an indicator of the presence of a complete P factor in experiments showing DNA transformation by injecting P-containing DNA into embryos.
Three features of the P system distinguish it from other transposable elements. One is the extremely high rate of transposition. Second is complete genetic control over transposition by choice of the appropriate maternal contribution. Third, the phenomenon is confined almost entirely to germ cells. These properties make the system particularly useful for a variety of genetic experiments, for example those using P factors as vehicles for cloning and DNA transformation.
The role of transposable elements as contributors to the spontaneous mutation rate is yet to be determined.
Keywords
- Transposable Element
- High Mutation Rate
- Female Sterility
- Chromosome Breakage
- Hybrid Dysgenesis
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
Paper Number 2667 from the Laboratory of Genetics.
This is a preview of subscription content, access via your institution.
Buying options
Preview
Unable to display preview. Download preview PDF.
References
Berg, R. L. (1974) A simultaneous mutability rise at thesingedlocus in two out of threeDrosophila melanogasterpopulations studied in 1973.Dros. Inf. Serv. 51: 100 – 102.
Berg, R. , W. R. Engels, and R. A. Kreber (1980) Site-specific X-chromosome rearrangements from hybrid dysgenesis inDrosophila melanogaster.Science207: 606 – 611.
Bingham, P. M. , M. G. Kidwell, and G. M. Rubin (1982) The molecular basis of P-M hybrid dysgenesis: The role of the P element, a P strain-specific transposon family.Cell29: 995 – 1004.
Bingham, P. M. , R. Levis, and G. M. Rubin (1981) The cloning of the DNA sequences from the white locus ofDrosophila melanogasterusing a novel and general method.Cell25: 693 – 704.
Bregliano, J. C. , and M. G. Kidwell (1983) Hybrid dysgenesis determinants, InMobile Genetic Elements, J. A. Shapiro, Ed. , Academic Press, New York, pp. 363 – 410.
Bregliano, J. C. , G. Picard, A. Bucheton, A. Pelisson, J. M. Lavige, and P. L’Heritier (1980) Hybrid dysgenesis inDrosophila melanogaster: The inducer-reactive system.Science207: 606 – 611.
Calos, M. P. , and J. H. Miller (1980) Transposable elements.Cell20: 579 – 595.
Chao, L. , C. Vargas, B. B. Spear, and E. C. Cox (1983) Transposable elements as mutator genes in evolution.Nature303: 633 – 635.
Cold Spring Harbor Symposia on Quantitative Biology(1981) Vol. 45. Cold Spring Harbor Laboratory, New York.
Cox, E. C. , and T. C. Gibson (1974) Selection for high nutation rates in chemostats.Genetics77: 169 – 184.
Damerec, M. (1937) Frequency of spontaneous mutations in certain stocks ofDrosophila melanogaster. Genetics22: 469 – 478.
Echols, H. (1981) SOS functions, cancer, and inducible evolution.Cell25: 1 – 2.
Eeken, J. C. J. , and F. H. Sobels (1981) Modification of MR activity in repair-deficient strains ofDrosophila melanogaster. Mut. Res. 83: 191 – 200.
Eeken, J. C. J. , and F. H. Sobels (1983) Modification of insertion mutation in prosophila by ENU, MMS, or deficient DNA-repair.Envir. Mut. 5: 456.
Engels, W. R. (1979) Extrachromosomal control of mutability inDrosophila melanogaster. Proc. Natl. Acad. Sci. USA76: 4011 – 4015.
Engels, W. R. (1979) Hybrid dysgenesis inDrosophila melanogaster: Rules of inheritance of female sterility. Genet. Res. 33: 219 – 234.
Engels, W. R. (1981) Germline hypermutability inDrosophilaand its relation to hybrid dysgenesis and cytotype.Genetics98: 565 – 587.
Engels, W. R. (1981) Hybrid dysgenesis inDrosophilaand the stochastic loss hypothesis.Cold Spring Harbor Synp. Quant. Biol. 45: 561 – 565.
Engels, W. R. (1981) Hybrid dysgenesis inDrosophilaand the stochastic loss hypothesis.Cold Spring Harbor Synp. Quant. Biol. 45: 561 – 565.
Engels, W. R. , and C. R. Preston (1979) Hybrid dysgenesis inDrosophila melanogaster: The biology of male and female sterility. Genetics 92: 161 – 174.
Engels, W. R. , and C. R. Preston (1981) Identifying P factors inDrosophilaby means of chromosome breakage hotspots. Cell 26: 421 – 428.
Goldschmidt, R. (1940) TheMaterial Basis of Evolution. Yale University Press, New Haven.
Green, M. M. (1970) The genetics of a mutator gene inDrosophila melanogaster. Mut. Res. 10: 353 – 363.
Green, M. M. (1976) Mutable and mutator loci, InThe Genetics and Biology of Drosophila, lb, M. Ashburner and E. Novitski, Eds. , Academic Press, New York, pp. 929 – 946.
Green, M. M. (1977) Genetic instability inDrosophila melanogaster:De novoinduction of putative insertion nutations.Proc. Natl. Acad. Sci. USA74: 3490 – 3493.
Hinton, C. W. (1981) Nucleocytoplasmic relations in a nutator-suppressor system ofDrosophila ananassae. Genetics98: 77 – 90.
Hinton, C. W. (1983) Relations between factors controlling crossing over and mutability in males ofDrosophila ananassae. Genetics104: 95 – 112.
Hiraizumi, Y. (1971) Spontaneous recombination inDrosophila melanogastermales.Proc. Natl. Acad. Sci. USA 68: 268 – 270.
Ising, G. , and K. Block (1981) Derivation-dependent distribution of insertion sites for aDrosophilatransposon. Cold Spring Harbor Symp. Quant. Biol. 45: 527 – 544.
Ising, G. , and C. Ramel (1973) A white-suppressor behaving as an episome inDrosophila melanogaster.Genetics74:sl23.
Ives, P. T. (1950) The importance of mutation rate genes in evolution.Evolution4: 236 – 252.
Kidwell, M. G. , J. F. Kidwell, and J. A. Sved (1977) Hybrid dysgenesis inDrosophila melanogaster: A syndrome of aberrant traits including mutation, sterility, and male recombination.Genetics86: 813 – 833.
Leigh, E. (1973) The evolution of mutation rates.Genetics73 (suppl): 1 – 18.
Levis, R. , M. Collins, and G. M. Rubin (1982) FB lements are the common basis for the instability of thewDZL andwCDrosophilamutations. Cell 30: 551 – 565.
Levitan, M. (1963) A maternal factor which breaks paternal chromosomes.Nature200: 437 – 438.
Lim, J. K. (1979) Site-specific instability inDrosophila melanogaster: The origin of the mutation and cytogenetic evidence for site specificity.Genetics93: 681 – 701.
Lim, J. K. (1979) Site-specific instability inDrosophila melanogaster: The origin of the mutation and cytogenetic evidence for site specificity.Genetics93: 681 – 701.
Mampell, K. (1943) High nutation frequency in Drosophilapseudoobscurarace B.Proc. Natl. Acad. Sci. USA29: 137 – 144.
Minamori, S. , and K. Ito (1971) Extrachromosomal element delta inDrosophila melanogaster. VI. Induction of recurrent lethal mutations in definite regions of second chromosomes. Mut. Res. 13: 361 – 369.
Moriwaki, D. , and Y. N. Tobari (1975)Drosophila ananassae. InHandbook of Genetics, Plenum Press, New York, Vol. 3, pp. 513–535.
Neel, J. V. (1942) A study of a case of high mutation rate inDrosophila melanogaster. Genetics 27: 519 – 536.
O’Hare, K. , and G. M. Rubin (1983) Structures of P transposable elements ofDrosophila melanogasterand their sites of insertion and excision. Cell 34: 25 – 35.
Orgel, L. E. , and F. H. C. Crick (1980) Selfish DNA: The ultimate parasite.Nature285: 604 – 607.
Picard, G. , J. C. Bregliano, A. Bucheton, J. M. Lavige, A. Pelisson, and M. G. Kidwell (1978) Non–Mendelian female sterility and hybrid dysgenesis inDrosophila melanogaster.Genet. Res. 32: 275 – 287.
Rubin, G. M. (1983) Dispersed repetitive DNAs in Drosophila, InMobile Genetic Elements, J. A. Shapiro, Ed. , Academic Press, New York, pp. 329 – 361.
Rubin, G. M. , M. G. Kidwell, and P. M. Bingham (1982) The molecular basis of P–M hybrid dysgenesis: The nature of induced mutations.Cell29: 987 – 994.
Rubin, G. M. , and A. C. Spradling (1982) Genetic transformationof Drosophilawith transposable element vectors.Science218: 348 – 353.
Sapienza, C. , and W. F. Doolittle (1981) Genes are things you have whether you want them or not.Cold Spring Harbor Symp. Quant. Biol. 45: 177 – 182.
Searles, L. L. , R. S. Jokerst, P. M. Bingham, R. A. Voelker, and A. L. Greenleaf (1983) Molecular cloning of sequences from aDrosophilaRNA polymerase locus by P element transposon tagging. Cell 31: 585 – 592.
Shapiro, J. A. , Ed. (1983)Mobile Genetic Elements, Academic Press, New York.
Simmons, M. J. , and J. K. Lim (1980) Site specificity of mutations arising in dysgenic hybrids ofDrosophila melanogaster. Proc. Natl. Acad. Sci. USA77: 6042 – 6046.
Slatko, B. E. , and Y. Hiraizumi (1973) Mutation induction in the male recombination strains ofDrosophila melanogaster. Genetics75: 643 – 649.
Spradling, A. C. , and G. M. Rubin (1982) Transposition of cloned P elements intoDrosophilagerm line chromosomes.Science218: 341 – 347.
Sturtevant, A. H. (1937) Essays on evolution. I. On the effects of selection on the mutation rate.Quart. Rev. Biol. 12: 464 – 467.
Sved, J. A. (1979) The hybrid dysgenesis syndrome inDrosophila melanogaster.Bioscience29: 659 – 664.
Sved, J. A. (1979) The hybrid dysgenesis syndrome inDrosophila melanogaster.Bioscience29: 659 – 664.
Thompson, J. N. , and R. C. Woodruff (1978) Mutator genes - pacemakers of evolution.Nature274: 317 – 321.
Truett, M. A. , R. S. Jones, and S. S. Potter (1981) Unusual structure of the FB family of transposable elements inDrosophila. Cell24: 753 – 763.
Voelker, R. A. (1974) The genetics and cytology of a mutator factor inDrosophila melanogaster. Mut. Res. 22: 265 – 276.
Yamaguchi, O. , R. Cardellino, and T. Mukai (1976) High rates of spontaneous chromosome aberrations inDrosophila melanogaster. Genetics83: 409 – 442.
Yamaguchi, O. , and T. Mukai (1974) Variation of spontaneous occurrence of chromosomal aberrations in the second chromosome ofDrosophila melanogaster.Genetics78: 1209 – 1221.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1984 Plenum Press, New York
About this chapter
Cite this chapter
Crow, J.F. (1984). The P-Factor: A Transposable Element in Drosophila. In: Chu, E.H.Y., Generoso, W.M. (eds) Mutation, Cancer, and Malformation. Environmental Science Research, vol 31. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2399-0_13
Download citation
DOI: https://doi.org/10.1007/978-1-4613-2399-0_13
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4612-9463-4
Online ISBN: 978-1-4613-2399-0
eBook Packages: Springer Book Archive