Chromosoma

, Volume 99, Issue 3, pp 231–236 | Cite as

Differential meiotic behaviour of diploid and tetraploid cells in a partially asynaptic mutant

  • J. L. Santos
Article
  • 28 Downloads

Abstract

A partially asynaptic individual of the grasshopperEuchorthippus pulvinatus (2n ♂ = 16 + X) was analysed at meiosis, using a Giemsa C-banding technique. Long chromosomes formed univalents less frequently than did medium and short ones. Homologues which succeeded in forming bivalents showed reduced chiasma frequency, the long chromosomes being affected by most. Changes in chiasma distribution were also observed. The presence of univalents at metaphase I seems to affect the function of the spindle, since most cells at the second division were unreduced. Cytokinesis was also subsequently suppressed in a great number of these products of restitution, resulting in the formation of diploid and tetraploid spermatids. Fifteen tetraploid metaphase I cells were also found in which pairing level and chiasma frequency were almost twice the average value in normal diploid individuals. The nature of this mutant is discussed.

Keywords

Developmental Biology Chiasma Frequency Meiotic Behaviour Tetraploid Cell Diploid Individual 
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.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Arana P, Santos JL, Giráldez R (1980) Chiasma interference and centromere co-orientation in a spontaneous translocation heterozygote of Euchorthippus pulvinatus gallicus (Acrididae; Orthoptera). Chromosoma 78:327–340Google Scholar
  2. Baker BS, Carpenter AT, Esposito MS, Sandler L (1976) The genetic control of meiosis. Annu Rev Genet 10:53–134Google Scholar
  3. Diez M, Puertas MJ (1981) Chiasma distribution in asynaptic Locusta migratoria. Chromosoma 84:431–437Google Scholar
  4. Driscoll CJ, Darvey NL, Barber HN (1967) Effect of colchicine on meiosis of hexaploid wheat. Nature 216:687–688Google Scholar
  5. Giráldez R, Santos JL (1981) Cytological evidence for preferences of identical over homologous but not-identical meiotic pairing. Chromosoma 82:447–451Google Scholar
  6. Golubovskaya IN (1979) Genetic control of meiosis. Int Rev Cytol 58:247–290Google Scholar
  7. Gottschalk W, Kaul MLH (1980a) Asynapsis and desynapsis in flowering plants. I. Asynapsis. Nucleus 23:1–5Google Scholar
  8. Gottschalk W, Kaul MLH (1980b) Asynapsis and desynapsis in flowering plants. II. Desynapsis. Nucleus 23:97–120Google Scholar
  9. John B, Henderson SA (1962) Asynapsis and polyploidy in Schistocerca paranensis. Chromosoma 13:114–147Google Scholar
  10. John B, Lewis KR (1965) Protoplasmatologia. I. The meiotic system. Springer, Berlin Heidelberg, p 335Google Scholar
  11. John B, Naylor B (1961) Anomalous chromosome behaviour in the germ line of Schistocerca gregaria. Heredity 16:187–198Google Scholar
  12. Jones GH, Croft JA (1986) Surface spreading of synaptonemal complexes in locusts. II. Zygotene pairing behaviour. Chromosoma 93:489–495Google Scholar
  13. Koduru PKR, Rao MK (1981) Cytogenetics of synaptic mutants in higher plants. Theor Appl Genet 59:197–214Google Scholar
  14. Koller PC (1938) Asynapsis in Pisum sativum. J Genet 36:275–306Google Scholar
  15. Li HW, Pao WK, Li Ch (1945) Desynapsis in common wheat. Am J Bot 32:92–101Google Scholar
  16. Omara MK, Hayward MD (1978) Asynapsis in Lolium perenne. Chromosoma 67:87–96Google Scholar
  17. Pi PH, Chao CY (1974) Microsporogenesis in Paspalum longifolium and P. commersonii on two different ploidy levels. Cytologia 39:453–465Google Scholar
  18. Prakken R (1943) Studies of asynapsis in rye. Hereditas 29:475–495Google Scholar
  19. Rees H (1957) Distribution of chiasmata in an “asynaptic” locust. Nature 180:559Google Scholar
  20. Richardson MM (1935) Meiosis in Crepis. II. Failure of pairing in Crepis capillaris (L.) WALLR. J Genet 31:119–143Google Scholar
  21. Rufas JS, Iturra P, de Souza W, Esponda P (1982) Simple silver staining procedure for the localization of nucleolus and nucleolar organizer under light and electron microscopy. Arch Biol 93:267–274Google Scholar
  22. Santos JL, Giráldez R (1978) The effect of C-heterochromatin in chiasma terminalization in Chorthippus biguttulus L. (Acrididae, Orthoptera). Chromosoma 70:59–66Google Scholar
  23. Santos JL, Giráldez R (1982) C-heterochromatin polymorphism and variation in chiasma localization in Euchorthippus pulvinatus gallicus (Acrididae, Orthoptera). Chromosoma 85:507–518Google Scholar
  24. Sjödin J (1970) Induced asynaptic mutants in Vicia faba L. Hereditas 66:215–232Google Scholar
  25. Soost RK (1951) Comparative cytology and genetics of asynaptic mutants in Lycopersicum esculentum MILL. Genetics 36:412–434Google Scholar
  26. Thomas H, Rajhathy T (1966) A gene for desynapsis and aneuploidy in tetraploid Avena. Can J Genet Cytol 8:506–515Google Scholar
  27. Zickler D, de Lares L, Moreau PJF, Leblon G (1985) Defective pairing and synaptonemal complex formation in a Sordaria mutant (spo44) with a translocated segment of the nucleolar organizer. Chromosoma 92:37–47Google Scholar

Copyright information

© Springer-Verlag 1990

Authors and Affiliations

  • J. L. Santos
    • 1
  1. 1.Departamento de Genética, Facultad de BiologiaUniversidad ComplutenseMadridSpain

Personalised recommendations