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Sequence and evolution of rhesus monkey alphoid DNA

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Summary

Analysis of rhesus monkey alphoid DNA suggests that it arose by tandem duplication of an ancestral monomer unit followed by independent variation within two adjacent monomers (one becoming more divergent than the other) before their amplification as a dimer unit to produce tandem arrays. The rhesus monkey alphoid DNA is a tandemly repeated, 343-bp dimer; the consensus dimer is over 98% homologous to the alphoid dimers reported for baboon and bonnet monkey, 81% homologous to the African green monkey alpha monomer, and less than 70% homologous to the more divergent human alphoid DNAs. The consensus dimer consists of two wings (I and II, 172 and 171 bp, respectively) that are only 70% homologous to each other, but share seven regions of exact homology. These same regions are highly conserved among the consensus sequences of the other cercopithecid alphoid DNAs. The three alpha-protein binding sites reported for African green monkey alpha DNA by F. Strauss and A. Varshavsky (Cell 37: 889–901, 1984) occur in wings I and II, but with one site altered in wing I. Two cloned dimer segments are 98% homologous to the consensus, each containing 8 single-base-pair differences within the 343-bp segment. Surprisingly, 37% of these differences occur in regions that are evolutionarily conserved in the alphoid consensus sequences, including the alpha-protein binding sites. Sequence variation in this highly repetitive DNA family may produce unique nucleosomal architectures for different members of an alphoid array. These unique architectures may modulate the evolution of these repetitive DNAs and may produce unique centromeric characteristics in primate chromosomes.

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Abbreviations

AGM:

African green monkey

EBr:

ethidium bromide

EDTA:

disodium ethylenediaminetetraacetate

PEG:

polyethylene glycol

RE:

restriction enzyme

RM:

rhesus monkey

I×SSC buffer:

0.15 M NaCl, 0.015 M sodium citrate, pH 7.0

TBE buffer:

50 mM Tris, 50 mM boric acid, 1 mM EDTA

References

  • Alwine JC, Kemp DJ, Parker BA, Reiser J, Renart J, Stark GR, Wahl GM (1979) Detection of specific RNAs or specific fragments of DNA by fractionation in gels and transfer to diazobenzyloxymethyl paper. Methods Enzymol 68:220–242

    PubMed  Google Scholar 

  • Birnboim HC, Doly J (1979) A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res 7:1513–1523

    PubMed  Google Scholar 

  • Brown FL, Musich PR, Maio JJ (1979) The repetitive sequence structure of component alpha DNA and its relationship to the nucleosomes of the African green monkey. J Mol Biol 131:777–799

    Article  PubMed  Google Scholar 

  • de Grouchy J, Turleau C, Finaz C (1978) Chromosomal phylogeny of the primates. Annu Rev Genet 12:289–328

    Article  PubMed  Google Scholar 

  • Donehower L, Furlong C, Gillespie D, Kurnit D (1980) DNA sequence of baboon highly repeated DNA: evidence for evolution by nonrandom unequal crossovers. Proc Natl Acad Sci USA 79:1497–1500

    Google Scholar 

  • Dretzen G, Bellard M, Sassone-Corsi P, Chambon P (1981) A reliable method for the recovery of DNA fragments from agarose and acrylamide gels. Anal Biochem 112:295–298

    Article  PubMed  Google Scholar 

  • Gray KM, White JW, Costanzi C, Gillespie D, Gillespie D, Schroeder WT, Calabretta B, Saunders GF (1985) Recent amplification of an alpha satellite DNA in humans. Nucleic Acids Res 13: 521–535

    PubMed  Google Scholar 

  • Hong S-B (1985) Studies on rhesus monkey alphoid DNA. Thesis, East Tennessee State University, Johnson City

    Google Scholar 

  • Horz W, Zachau HG (1977) Characterization of distinct segments in mouse satellite DNA by restriction nucleases. Eur J Biochem 73:383–392

    Article  PubMed  Google Scholar 

  • Johnson DA, Gautsch JW, Sportsman JR, Elder JH (1984) Improved technique utilizing nonfat dry milk for analysis of proteins and nucleic acids transferred to nitrocellulose. Gene Anal Techniques 1:3–8

    Article  Google Scholar 

  • King MC, Wilson AC (1975) Evolution at two levels in humans and chimpanzees. Science 188:107–116

    PubMed  Google Scholar 

  • Kurnit DM, Maio JJ (1973) Subnuclear redistribution of DNA species in confluent and growing mammalian cells. Chromosoma 2:23–36

    Article  Google Scholar 

  • Lam BS, Carroll D (1983) Tandomly repeated DNA sequences fromXenopus laevis I. Studies on sequence organization and variation in satellite I DNA (741 base-pair repeat). J Mol Biol 165:567–585

    PubMed  Google Scholar 

  • Maio J (1971) DNA strand reassociation and polynucleotide binding in the African green monkeyCercopithecus aethiops. J Mol Biol 56:579–595

    Article  PubMed  Google Scholar 

  • Maio JJ, Brown FL, Musich PR (1977) Subunit structure of chromatin and the organization of eukaryotic highly repetitive DNA: recurrent periodicities and models for the evolutionary origins of repetitive DNA. J Mol Biol 117:637–655

    Article  PubMed  Google Scholar 

  • Maio JJ, Brown FL, Musich PR (1981) Toward a molecular paleontology of primate genomes I. The HindIII and EcoRI dimer families of alphoid DNA. Chromosoma 83:103–125

    Article  PubMed  Google Scholar 

  • Maniatis AM, Fritsch EF, Sambrook J (1982) Molecular cloning. Cold Spring Harbor Laboratory. Cold Spring Harbor, New York

    Google Scholar 

  • Manuelidis L, Ward DC (1984) Chromosomal and nuclear distribution of the HindIII 1.9-kb human DNA repeat segment. Chromosoma 91:28–38

    Article  PubMed  Google Scholar 

  • Manuelidis L, Wu JC (1978) Homology between human and simian repeated DNA. Nature 276:92–94

    Article  PubMed  Google Scholar 

  • Maxam AM, Gilbert W (1980) Sequencing end-labeled DNA with base-specific chemical cleavages. Methods Enzymol 65: 499–560

    PubMed  Google Scholar 

  • Musich PR, Brown FL, Maio JJ (1977a) Subunit structure of chromatin and the organization of eukaryotic highly repetitive DNA: nucleosomal proteins associated with a highly repetitive mammalian DNA. Proc Natl Acad Sci USA 74:3297–3301

    PubMed  Google Scholar 

  • Musich PR, Maio JJ, Brown FL (1977b) Subunit structure of chromatin and the organization of eukaryotic highly repetitive DNA: indications of a phase relation between restriction sites and chromatin subunits in African green monkey and calf nuclei. J Mol Biol 117:657–677

    Article  PubMed  Google Scholar 

  • Musich PR, Brown FL, Maio JJ (1980) Highly repetitive component alpha and related alphoid DNAs in man and monkeys. Chromosoma 80:331–348

    Article  PubMed  Google Scholar 

  • Musich PR, Brown FL, Maio JJ (1982) Nucleosome phasing and micrococcal nuclease cleavage of African green monkey component alpha DNA. Proc Natl Acad Sci USA 79:118–122

    PubMed  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

    PubMed  Google Scholar 

  • Rosenberg H, Singer M (1978) Highly reiterated sequence of simiansimiansimiansimiansimian. Science 200: 394–402

    PubMed  Google Scholar 

  • Rubin CM, Deininger PL, Houck CM, Schmid CW (1980) A dimer satellite sequence in bonnet monkey DNA consists of distinct monomer subunits. J Mol Biol 136:151–167

    Article  PubMed  Google Scholar 

  • Schleif RF, Wensink PC (1981) Practical methods in molecular biology. Springer-Verlag, New York, p 97

    Google Scholar 

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

    Article  PubMed  Google Scholar 

  • Smith GP (1976) Evolution of repeated DNA sequence by unequal crossover. Science 193:528–535

    Google Scholar 

  • Southern EM (1975) Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 98:503–517

    PubMed  Google Scholar 

  • Strauss F, Varshavsky A (1984) A protein binds to a satellite DNA repeat at three specific sites that would be brought into mutual proximity by DNA folding in the nucleosome. Cell 37:889–901

    Article  PubMed  Google Scholar 

  • Thayer RE, Singer MF, McCutchan TF (1981) Sequence relationships between single repeat units of highly reiterated African green monkey DNA. Nucleic Acids Res 9:169–181

    PubMed  Google Scholar 

  • Wittig B, Wittig S (1979) A phase relationship associates tRNA structural gene sequences with nucleosome cores. Cell 18: 1173–1183

    Article  PubMed  Google Scholar 

  • Wu JC, Manuelidis L (1980) Sequence definition and organization of a human repeated DNA. J Mol Biol 142:363–386

    Article  PubMed  Google Scholar 

  • Zassenhaus HP, Butow RA, Hannon YP (1982) Rapid electroelution of nucleic acids from agarose and acrylamide gels. Anal Biochem 125:125–130

    Article  PubMed  Google Scholar 

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Pike, L.M., Carlisle, A., Newell, C. et al. Sequence and evolution of rhesus monkey alphoid DNA. J Mol Evol 23, 127–137 (1986). https://doi.org/10.1007/BF02099907

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  • DOI: https://doi.org/10.1007/BF02099907

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