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Karyotypic evolution of a novel cervid satellite DNA family isolated by microdissection from the Indian muntjac Y-chromosome

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Abstract

A minilibrary was constructed from DOP-PCR products using microdissected Y-chromosomes of Indian muntjac as DNA templates. Two microclones designated as IM-Y4-52 and IM-Y5-7 were obtained from negative screening of all three cervid satellite DNAs (satellites I, II, and IV). These two microclones were 295 and 382 bp in size, respectively, and shared ∼70% sequence homology. Southern blot analysis showed that the IM-Y4-52 clone was repetitive in nature with an ∼0.32-kb register in HaeIII digest. Sequence comparison revealed no similarities to DNA sequences deposited in the GenBank database, suggesting that the microclone sequences were from a novel satellite DNA family designated as cervid satellite V. A subclone of an Indian muntjac BAC clone which screened positive for IM-Y4-52 had a 3,325-bp insert containing six intact monomers, four deleted monomers, and two partial monomers. The consensus sequence of the monomer was 328 bp in length and shared more than 80% sequence homology with every intact monomer. A zoo blot study using IM-Y4-52 as a probe showed that the strong hybridization with EcoRI digested male genomic DNA of Indian muntjac, Formosan muntjac, Chinese muntjac, sambar deer, and Chinese water deer. Female genomic DNA of Indian muntjac, Chinese water deer, and Formosan muntjac also showed positive hybridization patterns. Satellite V was found to specifically localize to the Y heterochromatin region of the muntjacs, sambar deer, and Chinese water deer and to chromosome 3 of Indian muntjac and the X-chromosome of Chinese water deer.

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References

  • Bogenberger J, Schnell H, Fittler F (1982) Characterization of X-chromosome specific satellite DNA of Muntiacus muntjac vaginalis. Chromosoma 87:9–20

    Google Scholar 

  • Brinkley BR, Valdivia MM, Tousson A, Brenner SL (1984) Compound kinetochores of the Indian muntjac. Evolution by linear fusion of unit kinetochores. Chromosoma 91:1–11

    Google Scholar 

  • Buntjer JB, Nijman IJ, Zijlstra C, Lenstra JA (1998) A satellite DNA element specific for roe deer (Capreolus capreolus). Chromosoma 107:1–5

    Google Scholar 

  • Chaves R, Guedes-Pinto H, Heslop-Harrison J, Schwarzacher T (2000) The species and chromosomal distribution of the centromeric alpha-satellite I sequence from sheep in the tribe Caprini and other Bovidae. Cytogenet Cell Genet 91:62–66

    Google Scholar 

  • Chiang PY, Lin CC, Liao SJ, Hsieh LJ, Li SY, Chao MC, Li YC (2004) Genetic analysis for two subspecies of the Reeve’s mantjac (Cervidae: Muntiacus reevesi) by karyotyping and satellite DNAs analyses. Zool Stud 43:749–758

    Google Scholar 

  • Choo KH, Vissel B, Brown R, Filby RG, Earle E (1988) Homologous alpha satellite sequences on human acrocentric chromosomes with selectivity for chromosomes 13, 14 and 21: implications for recombination between nonhomologues and Robertsonian translocations. Nucleic Acids Res 16:1273–1284

    Google Scholar 

  • Elder FFB, Hsu TC (1988) Tandem fusion in the evolution of mammalian chromosomes. In: Sandberg AA (ed) The cytogenetics of mammalian autochromosomal rearrangements. Alan R. Liss, New York, pp 481–506

    Google Scholar 

  • Engelen JJ, Albrechts JC, Loots WJ, Hollanders-Crombach BH, Hamers AJ, Geraedts JP (1996) Application of micro-FISH to delineate deletions. Cytogenet Cell Genet 75:167–171

    Google Scholar 

  • Ferguson-Smith MA (1973) Human autosomal polymorphism and the non-random involvement of chromosomes in translocations. Chromosomes Today 4:235–246

    Google Scholar 

  • Fontana F, Rubini M (1990) Chromosomal evolution in Cervidae. Biosystems 24:157–174

    Google Scholar 

  • Fronicke L, Scherthan H (1997) Zoo-fluorescence in situ hybridization analysis of human and Indian muntjac karyotypes (Muntiacus muntjac vaginalis) reveals satellite DNA clusters at the margins of conserved syntenic segments. Chromosome Res 5:254–261

    Article  CAS  PubMed  Google Scholar 

  • Hartmann N, Scherthan H (2004) Characterization of ancestral chromosome fusion points in the Indian muntjac deer. Chromosoma 112:213–220

    Article  CAS  PubMed  Google Scholar 

  • Hsu TC, Pathak S, Chen TR (1975) The possibility of latent centromeres and a proposed nomenclature for total chromosome and whole arm translocations. Cytogenet Cell Genet 15:41–49

    Google Scholar 

  • Lan H, Wang W, Shi LM (1995) Phylogeny of Muntiacus (Cervidae) based on mitochondrial DNA RFLPs. Biochem Genet 33:377–388

    Google Scholar 

  • Lee C, Lin CC (1996) Conservation of a 31-bp bovine subrepeat in centromeric satellite DNA monomers of Cervus elaphus and other cervid species. Chromosome Res 4:427–435

    Google Scholar 

  • Lee C, Sasi R, Lin CC (1993) Interstitial localization of telomeric DNA sequences in the Indian muntjac chromosomes: further evidence for tandem chromosome fusions in the karyotypic evolution of the Asian muntjacs. Cytogenet Cell Genet 63:156–159

    Google Scholar 

  • Lee C, Ritchie DBC, Lin CC (1994) A tandemly repetitive, centromeric DNA sequence from the Canadian woodland caribou (Rangifer tarandus caribou): its conservation and evolution in several deer species. Chromosome Res 2:293–306

    Google Scholar 

  • Lee C, Court DR, Cho C, Haslett J, Lin CC (1997) High-order organization of subrepeats and the evolution of cervid satellite I DNA. J Mol Evol 44:327–335

    Google Scholar 

  • Lee C, Griffin DK, O’Brien PC, Yang F, Lin CC, Ferguson-Smith MA (1998) Defining the anatomy of the Rangifer tarandus sex chromosomes. Chromosoma 107:61–69

    Google Scholar 

  • Lee C, Stanyon R, Lin CC, Ferguson-Smith MA (1999) Conservation of human gamma-X centromeric DNA among primates with an autosomal location in certain Old World monkeys. Chromosome Res 7:43–47

    Google Scholar 

  • Li YC, Lee C, Hseu TH, Li SY, Lin CC (2000a) Direct visualization of the genomic distribution and organization of two cervid centromeric satellite DNA families. Cytogenet Cell Genet 89:192–198

    Google Scholar 

  • Li YC, Lee C, Li SY, Lin CC (2000b) Centromeric heterochromatin packaging and centromeric protein binding. Am J Hum Genet 67(Suppl 2):A815

    Google Scholar 

  • Li YC, Lee C, Sanoudou D, Hseu TH, Li SY, Lin CC (2000c) Interstitial colocalization of two cervid satellites DNAs involved in the genesis of the Indian muntjac karyotype. Chromosome Res 8:363–373

    Google Scholar 

  • Li YC, Lee C, Chang WS, Li SY, Lin CC (2002) Isolation and identification of a novel satellite DNA family highly conserved in several Cervidae species. Chromosoma 111:176–183

    Google Scholar 

  • Lin CC, Sasi R, Fan YS, Chen ZQ (1991) New evidence for tandem chromosome fusions in the karyotypic evolution of Asian muntjacs. Chromosoma 101:19–24

    CAS  PubMed  Google Scholar 

  • Lin CC, Chiang PY, Hsieh LJ, Chao MC, Li YC (2004) Cloning, characterization and physical mapping of three cervid satellite DNA families in the genome of Formosan muntjac (Muntiacus reevesi micrurus). Cytogenet Genome Res 105:100–106

    Google Scholar 

  • Ma SL, Wang YX, Xu LH (1986) Taxonomic and phylogenetic studies on the genus Muntiacus. Acta Theriol Sin 6:191–207

    Google Scholar 

  • Neitzel H (1987) Chromosome evolution of cervidae: karyotypic and molecular aspects. In: Obe G, Basler A (eds) Cytogenetics. Springer, Berlin Heidelberg New York, pp 90–112

    Google Scholar 

  • Page SL, Shin JC, Han JY, Choo KH, Shaffer LG (1996) Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation. Hum Mol Genet 5:1279–1288

    Google Scholar 

  • Pomp D, Good BA, Geisert RD, Corbin CJ, Conley AJ (1995) Sex identification in mammals with polymerase chain reaction and its use to examine sex effects on diameter of day-10 or -11 pig embryos. J Anim Sci 73:1408–1415

    Google Scholar 

  • Qureshi SA, Blake RD (1995) Sequence characteristic of a cervid DNA repeat family. J Mol Biol 158:293–304

    Google Scholar 

  • Randi E, Mucci N, Pierpaoli M, Douzery E (1998) New phylogenetic perspectives on the Cervidae (Artiodactyla) are provided by the mitochondrial cytochrome b gene. Proc R Soc Lond B Biol Sci 265:793–801

    Google Scholar 

  • Rattner JB (1986) Organization within the mammalian kinetochore. Chromosoma 93:515–520

    Google Scholar 

  • Scherthan H (1990) Localization of the repetitive telomeric sequence (TTAGGG)n in two muntjac species and implications for their karyotypic evolution. Cytogenet Cell Genet 53:115–117

    Google Scholar 

  • Scherthan H (1995) Chromosome evolution in muntjac revealed by centromere, telomere and whole chromosome paint probes. Kew Chromosome Conf IV:267–280

    Google Scholar 

  • Schmidtke J, Brennecke H, Schmid M, Neitzel H, Sperling K (1981) Evolution of muntjac DNA. Chromosoma 84:187–193

    Google Scholar 

  • Shi LM, Pathak S (1981) Gametogenesis in an Indian muntjac×Chinese muntjac hybrid. Cytogenet Cell Genet 30:152–156

    Google Scholar 

  • Shi LM, Ye YY, Duan XS (1980) Comparative cytogenetic studies on the red muntjac, Chinese muntjac and their F1 hybrids. Cytogenet Cell Genet 26:22–27

    Google Scholar 

  • Slamovits CH, Rossi MS (2002) Satellite DNA: agent of chromosomal evolution in mammals. A review. J Neotrop Mammal 9:297–308

    Google Scholar 

  • Telenius H, Carter NP, Bebb CE, Nordenskjold M, Ponder BA, Tunnacliffe A (1992) Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics 13:718–725

    CAS  PubMed  Google Scholar 

  • Wang W, Lan H (2000) Rapid and parallel chromosomal number reductions in muntjac deer inferred from mitochondrial DNA phylogeny. Mol Biol Evol 17:1326–1333

    Google Scholar 

  • Whitehead GK (1972) Deer of the world. Constable and Company, London, p 194

    Google Scholar 

  • Wichman HA, Payne CT, Ryder OA, Hamilton MJ, Maltbie M, Baker RJ (1991) Genomic distribution of heterochromatic sequences in equids: implication to rapid chromosomal evolution. J Heredity 82:369–377

    Google Scholar 

  • Yang F, Carter NP, Shi L, Ferguson-Smith MA (1995) A comparative study of karyotypes of muntjacs by chromosome painting. Chromosoma 103:642–652

    Article  CAS  PubMed  Google Scholar 

  • Yang F, O’Brien PCM, Wienberg J, Ferguson-Smith MA (1997a) A reappraisal of the tandem fusion theory of karyotype evolution in the Indian muntjac using chromosome painting. Chromosome Res 5:109–117

    Article  CAS  PubMed  Google Scholar 

  • Yang F, O’Brien PCM, Wienberg J, Neitzel H, Lin CC, Ferguson-Smith MA (1997b) Chromosomal evolution of Chinese muntjacs (Muntiacus reevesi). Chromosoma 106:37–43

    Google Scholar 

Download references

Acknowledgements

This study was supported by grants from the National Science Council, Taiwan (NSC92-2320-B-040-048), and from the National Health Research Institute, Taiwan (NHRI-EX92-9207SI). We thank Leona Chemnick and Susan Hansen for help with sample inventory and transfer, including documentation required under US regulations.

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Correspondence to C. C. Lin.

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Communicated by E.A. Nigg

Y.-C. Li and Y.-M. Cheng contributed equally to this work.

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Li, YC., Cheng, YM., Hsieh, LJ. et al. Karyotypic evolution of a novel cervid satellite DNA family isolated by microdissection from the Indian muntjac Y-chromosome. Chromosoma 114, 28–38 (2005). https://doi.org/10.1007/s00412-005-0335-7

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