Abstract
Recombination frequency, chiasmata and chromatid interference were studied by means of analysis of meiotic configurations in diakinesis and metaphase II in single and double heterozygotes for the partially overlapping inversions In(1)1Rk and In(1)12Rk in chromosome 1 of the house mouse. Recombination frequency in the inverted regions was decreased in single heterozygotes and increased in the double heterozygotes as compared to normal homozygotes. Chiasmata in the inverted regions in the double heterozygotes did not interfere with each other. A significant excess of 4-chromatid double exchanges in the inverted regions was detected in the double heterozygotes.
References
Agulnik, S I, Agulnik, A I, and Ruvinsky, A O. 1986. Recombination distances between the loci in the proximal part of the chromosome 17 in female heterozygous for translocations Rb(8,17)1IEM, Rb(16,17)7Bnr, and T(16;17)43H. Mouse News Lett, 75, 34–35.
Arana, P, Santos, L, and Giraldez, R. 1980. Chiasma interference and centromere co-orientation in a spontaneous translocation heterozygote of Euchorthippus pulvinatus gallicus (Acrididae; Orthoptera). Chromosoma, 78, 327–340.
Ashley, T. 1990. G-bands and chromosomal meiotic behaviour. Chromosomes Today, 10, 311–320.
Borodin, P M, Gorlov, I P, Agulnik, A I, Agulnik, S I, and Ruvinsky, A O. 1991. Chromosome pairing and recombination in mice heterozygous for different translocations in chromosomes 16 and 17. Chromosoma, 101, 252–258.
Borodin, P M, Gorlov, I P, and Ladygina, T YU. 1990a. Synapsis in single and double heterozygotes for partially overlapping inversions in chromosome 1 of the house mouse. Chromosoma, 99, 365–370.
Borodin, P M, Gorlov, I P, and Ladygina, T YU. 1990b. Double insertion of homogeneously staining regions in chromosome 1 of wild Mus musculus musculus: effects on chromosome pairing and recombination. J Hered, 81, 91–95.
Borodin, P M, Gorlov, I P, and Ladygina, T YU. 1992. Synaptic interrelationships between the segments of the hetero-morphic bivalent in double heterozygotes for paracentric inversions in chromosome 1 of the house mouse. Chromosoma, 101, 374–379.
Chandley, A C. 1982. A pachytene analysis of two male-fertile paracentric inversions in chromosome 1 of the mouse and in the male-sterile double heterozygote. Chromosoma, 85, 127–135.
Chandley, A C. 1986. A model for effective pairing and recombination at meiosis of early replicating sites (R- bands) along chromosomes. Hum Genet, 72, 50–57.
Chandley, A C. 1990. Repetitive sequences as promoters of pairing at meiosis and the consequence of misalignment for de novo mutation in man. Chromosomes Today, 10, 321–328.
Davisson, M T, and Roderick, T H. 1973. Chromosomal banding patterns of two paracentric inversions in mice. Cytogenet Cell Genet, 12, 398–403.
Evans, E P, Beechey, C V, Burtenshaw, M D, and Searle, A G. 1993. T(In1;5), a complex mouse chromosomal rearrangement with phenotypic effect. Cytogenet Cell Genet, 66, 66–72.
Evans, E P, Breckon, G, and Ford, C D. 1964. An air-drying method for meiotic preparations from mammalian testes. Cytogenetics, 3, 289–299.
Evans, E P, and Ford, C E. 1976. Some cytological properties of paracentric inversions in the mouse. In: Jones, K. and Brandham, P. E. (eds) Current Chromosome Research. Kew Chromosome Conference, pp. 216–217. Elsevier/North Holland Biomedical Press, Amsterdam.
Ford, C E, Evans, E P, and Burtenshaw, M D. 1976. Meiosis and fertility in mice heterozygous for paracentric inversions. In: Jones, K. and Brandham, P. E. (eds) Current Chromosome Research. Kew Chromosome Conference, pp. 123–132. Elsevier/North Holland Biomedical Press, Amsterdam.
Forejt, J. 1973. Centromeric heterochromatin polymorphism in the house mouse. Evidence from inbred strains and natural populations. Chromosoma, 43, 187–201.
Gorlov, I P, Ladygina, T YU, and Borodin, P M. 1993. Chiasma distribution in the first bivalent of mice carrying a double insertion of homogeneously-staining regions in homozygous and heterozygous states. Heredity, 70, 642–647.
Gorlov, I P, Ladygina, T, Yu Serov, O L, and Borodin, P M. 1991. Positional control of chiasma distribution in the house mouse. Chiasma distribution in mice homozygous and heterozygous for an inversion in chromosome 1. Heredity, 66, 453–458.
Hewitt, G M. 1967. An interchange which raises chiasma frequency. Chromosoma, 21, 285–295.
Haldane, J B S. 1931. The cytological basis of genetical interference. Cytologia (Tokyo), 3, 54–65.
Jones, G H. 1987. Chiasmata. In: Moens, P. B. (ed.) Meiosis, pp. 213–245. Academic Press, Orlando, FL.
Jones, G N, and Tease, C. 1979. Analysis of exchanges in differentially stained meiotic chromosomes of Locusta migratoria after Brdu-substitution and FPG staining. Chromosoma, 73, 85–91.
Kanda, N, and Kato, H. 1980. Analysis of crossing over in mouse meiotic cells by Brdu labelling technique. Chromosoma, 78, 113–121.
Maguire, M P. 1988. Interactive meiotic systems. In: Gustafson, J. P. and Appels, R. (eds) Chromosome Structure and Function Impact of New Concepts, pp. 117–144. Plenum Press, New York.
Moens, P B. 1985. Research needs in meiosis, mechanisms of synapsis, and chiasma regulation. In: Dellarco, V. L., Voytek, P. E. and Hollander, A. (eds) Aneuploidy, Etiology and Mechanisms, pp. 397–408. Plenum Press, New York, London.
Mortimer, R K, and Fogel, S. 1985. Genetic interference and gene conversion. In: Grell, R. F. (ed.) Mechanisms of Recombination, pp. 263–292. Plenum Press, New York, London.
Moses, M J. 1980. New cytogenetic studies on mammalian meiosis. In: Serio, M. and Martini, L. (eds) Animal Models in Human Reproduction, pp. 169–190. Academic Press, New York.
Parker, J S. 1987. Increased chiasma frequency as a result of chromosome rearrangement. Heredity, 58, 87–94.
Parker, J S, Pamer, R W, Whitehorn, M A F, and Edgar, L A. 1982. Chiasma frequency effects of structural chromosome change. Chromosoma, 85, 673–686.
Searle, A G, and Beechey, C V. 1989. Map of reciprocal translocations, inversions and insertions. In: Lyon, M. F. and Searle, A. G. (eds) Genetic Variants and Strains of the Laboratory Mouse, 2nd edn., pp. 620–626. Oxford University Press/Gustav Fisher, Stuttgart.
Sturtevant, A H. 1926. A crossover reducer in Drosophila melanogaster due to an inversion of a section of the third chromosome. Biol Zbl, 46, 697–702.
Sumner, A T. 1972. A simple technique for demonstrating centromeric heterochromatin. Exp Cell Res, 75, 304–306.
Sybenga, J. 1975. Meiotic configurations. In: Frankel, R. (ed.) Monographs on Theoretical and Applied Genetics 1, pp. 1–25. Springer, Berlin, New York.
Van Der Linden, A G J M, Pearson, P L, and Van Der Kamp, J J P. 1975. Cytological assessment of meiotic exchange in a human male with pericentric inversion of chromosome no. 4. Cytogenet Cell Genet, 14, 126–132.
Acknowledgements
We thank Dr ?. ?. Roderick for the gift of mice homozygous for Inl and Inl2, Dr A. C. Chandley for valuable suggestions, Mrs M. Rodionova, Mrs O. Gorlova and Ms T. Ladygina for assistance. This work is supported by the National Genetic Research Fund.
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Gorlov, I., Borodin, P. Recombination in single and double heterozygotes for two partially overlapping inversions in chromosome 1 of the house mouse. Heredity 75, 113–125 (1995). https://doi.org/10.1038/hdy.1995.114
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DOI: https://doi.org/10.1038/hdy.1995.114
Keywords
- chromatid interference
- house mouse
- mouse chromosome 1
- overlapping inversions
- recombination frequency
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