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Satellite DNA I in chromatin loops of rat pachytene chromosomes and in spermatids

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Abstract

Biotinylated rat satellite DNA I probe p93-50 was used to visualize the chromatin of surface-spread rat pachytene chromosomes. Fluorescein isothiocyanate (FITC)-conjugated avidin produces a beaded fluorescence pattern along the chromatin loops that insert in the centromeric region of the synaptonemal complex (SC), the paired cores of homologous chromosomes. The number of fluorescent beads ranges from zero for centromeres without satellite DNA I homologous to probe p 93-50, to several hundred for satellite-rich centromeric regions. For the chromosomes that can be identified, the relative amount of satellite DNA is chromosome specific. No satellite DNA I was detected at the non-centromeric ends of the chromosomes or interstitially. DNase-digested nuclei or isolated SCs did not have detectable amounts of satellite DNA in the centromeric regions of the chromosomes or in the residual SCs. The fate of the satellite DNA was followed during spermiogenesis. In the round spermatid the centromeric regions, which appear to be attached to the nuclear envelope, are still distinct and have converging loops of fluorescent chromatin. At later stages there are fewer but still bright fluorescent patches. Satellite DNA I is still detectable in the mature sperm head. These results demonstrate the organization of satellite DNA I in the chromatin loops at the centromeric regions, and they forecast the analysis of chromosome organization in unprecedented detail with a variety of probes in surface spreads of meiotic prophase chromosomes.

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References

  • Brinkley BR, Brenner SL, Hall JM, Tousson A, Balczon RD, Valdivia MM (1986) Arrangements of kinetochores in mouse cells during meiosis and spermiogenesis. Chromosoma 94:309–3417

    Google Scholar 

  • Counce SJ, Meyer GF (1973) Differentiation of the synaptonemal complex and the kinetochore in Locusta spermatocytes studied by whole mount electron microscopy. Chromosoma 44:231–253

    Google Scholar 

  • Cremisi F, Vignali R, Batistoni R, Barsacchi G (1988) Heterochromatic DNA in Triturus (Amphibia, Urodela) II. A centromeric satellite DNA. Chromosoma 97:204–211

    Google Scholar 

  • Dresser ME (1987) The synaptonemal complex and meiosis: an immunocytochemical approach. In: Moens PB (ed) Meiosis. Academic Press, New York, pp 245–274

    Google Scholar 

  • Dresser ME, Moses MJ (1980) Synaptonemal complex karyotyping of the Chinese hamster (Cricetulus griseus). IX. Light and electron microscopy of synapsis and nucleolar development by silver staining. Chromosoma 76:1–22

    Google Scholar 

  • Feinberg AP, Vogelstein B (1983) A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 132:6–13

    Google Scholar 

  • Heyting C, Dettmers RJ, Dietrich AJJ, Redeker EJW, Vink ACG (1988) Two major components of the synaptonemal complex are specific for meiotic prophase nuclei. Chromosoma 96:325–332

    Google Scholar 

  • Heyting C, Dietrich AJJ, Moens PB, Dettmers RJ, Offenberg HH, Redeker EJW, Vink ACG (1989) Synaptonemal complex proteins. Genome 31:81–87

    Google Scholar 

  • Hutchison NJ, Langer-Safer PR, Ward DC, Hamkalo BA (1982) In situ hybridization at the electron microscope level: hybrid detection by autoradiography and colloidal gold. J Cell Biol 95:609–618

    Google Scholar 

  • Lawrence JB, Villnave CA, Singer RH (1988) Sensitive, high-resolution chromatin and chromosome mapping in situ: Presence and orientation of two closely integrated copies of EBV in a lymphoma line. Cell 52:51–61

    Google Scholar 

  • Li S, Meistrich ML, Brock WA, Hsu TC, Kuo MT (1983) Isolation and preliminary characterization of the synaptonemal complex from rat pachytene spermatocytes. Exp Cell Res 144:63–72

    Google Scholar 

  • Maniatis T, Fritsch EF, Sambrook J (1982) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, NY

    Google Scholar 

  • Manuelidis L, Langer-Safer PR, Ward DC (1982) High-resolution mapping of satellite DNA using biotin-labeled DNA probes. J Cell Biol 95:619–625

    Google Scholar 

  • Mitchell AR, Ambros P, McBeath S, Chandley AC (1986) Molecular hybridization to meiotic chromosomes in man reveals sequence arrangement on the No. 9 chromosome and provides clues to the nature of “parameres”. Cytogenet Cell Genet 41:89–95

    Google Scholar 

  • Moens PB (1978) Lateral element cross connections of the synaptonemal complex and their relationship to chiasmata in rat spermatocytes. Can J Genet Cytol 20:567–579

    Google Scholar 

  • Moens PB, Earnshaw WC (1989) Anti-topoisomerase II recognizes meiotic chromosome cores. Chromosoma, in press

  • Moens PB, Pearlman RE (1988) Chromatin organization at meiosis. BioEssays 9:151–153

    Google Scholar 

  • Moens PB, Heyting C, Dietrich AJJ, van Raamsdonk W, Chen Q (1987) Synaptonemal complex antigen location and conservation. J Cell Biol 105:93–103

    Google Scholar 

  • Pech M, Igo-Kemenes T, Zachau HG (1979) Nucleotide sequence of a highly repetitive component of rat DNA. Nucleic Acids Res 7:417–432

    Google Scholar 

  • Radic MZ, Lundgren K, Hamkalo BA (1987) Curvature of mouse satellite DNA and condensation of heterochromatin. Cell 50:1101–1108

    Google Scholar 

  • Sealy L, Hartley J, Donelson J, Chalkley R, Hutchison N, Hamkalo BA (1981) Characterization of a highly repetitive sequence DNA family in rat. J Mol Biol 145:291–318

    Google Scholar 

  • Shen D, Wang Z, Wu M (1987) Gene mapping on maize pachytene chromosomes by in situ hybridization. Chromosoma 95:311–314

    Google Scholar 

  • von Wettstein D, Rasmussen SW, Holm PB (1984) The synaptonemal complex in genetic segregation. Annu Rev Genet 18:331–431

    Google Scholar 

  • Waye JS, Willard HF (1989) Chromosome specificity of satellite DNAs: short- and long-range organization of a diverged dimeric subset of human alpha satellite from chromosome 3. Chromosoma 97:475–480

    Google Scholar 

  • Weith A, Traut W (1980) Synaptonemal complexes with associated chromatin in a moth, Ephestia kuehniella Z. Chromosoma 78:275–291

    Google Scholar 

  • Witney FR, Furano AV (1983) The independent evolution of two closely related satellite DNA elements in rats (Rattus). Nucleic Acids Res 11:291–304

    Google Scholar 

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Moens, P.B., Pearlman, R.E. Satellite DNA I in chromatin loops of rat pachytene chromosomes and in spermatids. Chromosoma 98, 287–294 (1989). https://doi.org/10.1007/BF00327315

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  • DOI: https://doi.org/10.1007/BF00327315

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