Добавил:
Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Клональное разнообразие и механизмы его формирования у однополых видов ящериц рода Darevskia. Монография

.pdf
Скачиваний:
0
Добавлен:
07.09.2026
Размер:
2 Мб
Скачать
Ê
ЛОНАЛЬНОЕ РАЗНООБРАЗИЕ И МЕХАНИЗМЫ ЕГО ФОРМИРОВАНИЯ У ЯЩЕРИЦ РОДА
Darevskia
armeniaca, D. dahli, D. rostombekowi и D. unisexualis. Определе­на структура и особенности этих локусов у однополых и роди­тельских бисексуальных видов рода Darevskia. В изученных по­пуляциях партеновидов выявлены аллельные варианты каждо­го локуса и определена нуклеотидная последовательность каж­дого аллеля.
Установлено, что:
― отличия аллелей связаны с вариациями в структуре
микросателлитных кластеров и с однонуклеотидны­ми заменами на фиксированных расстояниях в при­лежащих к кластеру участках ДНК;
― однонуклеотидные вариации вместе с прилежащим
микросателлитом формируют гаплотипические мар­керы (гаплотипы), специфические для каждого ал­леля;
― гаплотипические маркеры наследуются от роди-
тельских двуполых видов
― сочетания гаплотипов образуют генотипы, отличаю-
щиеся по частоте встречаемости и распределению в популяциях;
― особи с одинаковыми генотипами образуют отдель-
ные клональные линии гибридного и постмутаци­онного происхождения;
полиморфные однонуклеотидные маркеры дают
прямую информацию о числе событий межвидовой гибридизации с образованием исходных гибридных клонов, а микросателлитные маркеры дают дополни­тельную информацию о возможных мутациях в ис­ходных гибридных клонах с образованием новых генотипов и клональных линий.
Разработанный нами подход генотипирования может найти универсальное приложение для оценки клонального разнообра­зия и определения его происхождения ных гибридного происхождения. Продолжение исследований по данной тематике может быть связано с привлечением для гено­типирования дополнительных локусов ядерного генома, опре­делением изменчивости митохондриальной ДНК, а также полно­геномным и транскриптомным секвенированием с последующим анализом совокупности полученных данных.
;
у любых видов живот-
g 81 G
À.À. Â
ЕРГУН
, À.Å. Ã
ИРНЫК
, Ô.À. Î
СИПОВ
, À.Â. Î
МЕЛЬЧЕНКО
СПИСОК ЛИТЕРАТУРЫ
1. A fine line between sex and unisexuality: the phylogenetic constraints on parthenogenesis in lacertid lizards / Murphy R. W., Fu J., Mac­Culloch R. D. et al. // Zoological Journal of Linnean Society. 2000. V. 130. Рp. 527549.
2. Aharoni A., Baran N., Manor H. Characterization of a multi-subunit human protein which selectively binds single stranded d(GA)
sequence repeats in DNA // Nucleic Acid Research. 1993. V.
d(GT)
n
21. Pp. 5221–5228.
3. A highly conserved repetitive DNA sequence, (TTAGGG) the telomeres of human chromosomes / Moyzis R. K., Buckingham J. M., Cram L. S. et al. // Proceedings of the National Academy of Sciences USA. 1988. V. 85. . 18. Pp. 66226626.
4. Aissani В., Bernardi G. CpG-islands: features and distribution in the genome of vertebrates // Gene. 1991. V. 106. Pp. 173183.
5. Alu repeats: a source for the genesis of primate microsatellites / Arcot S. S., Wang Z., Weber J. L. et al. // Genomics. 1995. V. 29. Pp. 136–144.
6. A novel unstable mouse VNTR family expanded from SINE B1 ele­ments / Bois P., Willianson J., Brown J. et al. // Genomics. 1998. V.
49. Pp.122–128.
7. Arribas O. J. Phylogeny and relationships of the mountain lizards of Europe and Near East (Archaeolacerta Merttens, 1921, Sensu Lato) and their relationships among the Eurasian Lacertid lizards // Russian Journal of Herpetology. 1999. V. 6. 1. Pp. 122.
8. Bernardi G. J. Compositional patterns, in Nuclear Genome of cold-blooded vertebrates // Journal of Molecular Evolution. 1990. V. 31. Pp. 265−281.
9. Bernardi G. J. Compositional properties of nuclear genes from cold­blooded vertebrates // Journal of Molecular Evolution. 1991. V. 33. Pp. 5767.
10. Bi K., Bogart J. P. Identification of intergenomic recombinations in unisexual slamanaders of the genus Ambystoma by genomic in situ hybridization // Cytogenet Genome Res. 2006. 112. Рp. 307–312.
11. Bi K., Bogart J. P. Time and time again: unisexual salamanders (genus Ambystoma) are the oldest unisexual vertebrates // BMC Evolutionary Biology. 2010. 10. Р. 238.
12. Bi K., Bogart J. P., Fu J. Genealogical relationships of southern On­tario polyploid unisexual salamanders (genus Ambystoma) inferred from intergenomic exchanges and major rDNA cytotypes // Chromo­some Res. 2008. 16. Рp. 275–289.
and
n
, present at
n
g 82 G
Ê
ЛОНАЛЬНОЕ РАЗНООБРАЗИЕ И МЕХАНИЗМЫ ЕГО ФОРМИРОВАНИЯ У ЯЩЕРИЦ РОДА
13. Bi K., Bogart J. P., Fu J. Intergenomic translocations in unisexual salamanders of the genus Ambystoma (Amphibia, Caudata) // Cytoge­net Genome Res. 2007. 116. Рp. 289–297.
14. Bi K., Bogart J. P., Fu J. Two rare aneutriploids in the unisexual Am- bystoma (Amphibia, Caudata) identified by GISH indicating two dif­ferent types of meiotic errors // Cytogenet Genome Res. 2007. 119. Рp. 127–130.
15. Bi K., Bogart J. P., Fu J. The prevalence of genome replacement in unisexualis salamanders of the genus Ambystoma (Amphibia, Cau­data) revealed by nuclear gene genealogy // BMC Evolutionary Biol­ogy. 2008. 8. Рp.158.
16. Biet E.,Sun J., Dutreix M. Conserved sequence preference in DNA binding among recombination proteins: an effect of ssDNA secondary structure // Nucleic Acids Research. 1999. V. 27. Pp. 596-600
17. Bogart J. P. Genetics and systematics of hybrid species // Reproduc­tive Biology and Phylogeny of Urodela. Volume 1 Enfield: M/s ScienceSever DM. 2003. Рp. 109–134.
18. Brohede J., Ellegren H. Microsatellite evolution: polarity of substitu­tions within repeats and neutrality of flanking sequences // The Royal Society. 1999. V. 266. Pp. 825–833.
19. Capriglione T. Repetitive DNA as a tool to study the phylogeny of cold-blooded vertebrates // Chromosomes Today. 2000. V. 13. Pp. 183194.
20. Capriglione T. Satellite DNA and phylogeny of Lacertid lizards // Scientia Herpetologica. 1995. V. 60. № 13. Pp. 68−70.
21. Chen Y., Roxby R. Identification of a functional CT-element in the Phytophthora infestans piyptl gene promoter // Gene. 1997. V.198. Pр.159–164.
22. Chromosome G-banding comparison among some mediterranean lacertid lizards / Odierna G., Capriglione Т., Caputo V. et al.; Eds: Valakos E. D., Böhme W., Perez-Mellado V., Maragou P. // Lacertid of the mediterranean region. 1993. Pр. 5159.
23. CHK1 frameshift mutations in genetically unstable colorectal and en­dometrial cancers / Bertoni F., Codegoni A. M., Furlan D. et al. // Genes Chromosomes Cancer. 1999. V. 26. Pp. 176–180.
24. Cimino M. C. Egg production, polyploidization and evolution in a diploid all-female fish of the genus Poeciliopsis // Evolution. 1972. V.
26. Pр. 294–306.
25. Clonal Diversity and Clone Formation in the Parthenogenetic Cauca­sian Rock Lizard Darevskia dahli / Vergun A.A., Martirosyan I.A., Semyenova S.K. et al. // PLoS ONE. 2014. V. 9(3). e91674. doi:10.1371/journal.pone.0091674
Darevskia
g 83 G
À.À. Â
ЕРГУН
, À.Å. Ã
ИРНЫК
, Ô.À. Î
СИПОВ
, À.Â. Î
МЕЛЬЧЕНКО
26. Clonal stability and mutation in the self-fertilizing hermaphroditic fish, Rivulus marmoratus / Laughlin T. F., Lubinski B. A., Park E. H. et al. // Journal of Heredity. 1995. V. 86. . 5. Рp. 399−402.
27. Clonal variations in the Caucasian rock lizard Lacerta armeniaca and its origin / Fu J., MacCulloch R. D., Murphy R. W. et al. // Amphib­reptil. 2000. 21(1). Pр. 83–89.
28. Cole C. J., Dessauer H. C., Barrowclough G. F.Hybrid origin of a unisexual species of whiptail lizard, Cnemidophorus neomexicanus, in western North America: new evidence and a review //Am Mus Novit.
1988. 2905. Рр. 1–38.
29. Cole C. J., Townsend C. R. Parthenogenetic species of reptiles / Reinboth R., Springer-Verlad E. D. (ed.) // Intersexuality in the Ani­mal Kindom. Berlin, 1975. Pp. 340355.
30. Csink A. K., Henikoff S. Something from nothing: the evolution and utility
of satellite repeats // Trends in Genetics. 1998. V. 14. Pp. 200−204.
31. Darevsky I. S. Evolution and Ecology of parthenogenesis in reptiles // Current Research of biology of amphibians and reptiles. – Oxford, Ohio, 1993. Pp. 209257.
32. Darevsky I. S. Rock lizards of the Caucasus: systematics, ecology and phylogenesis of the polymorphic groups of Caucasian rock lizards of the subgenus Archaeolacerta // Leningrad: Nauka, 1967. Pp.1–216 [in Russian: English translation published by Indian Natl Sci Doc Ctr, New Delhi, 1978].
33. Darevsky I. S., Kupriyanova L. A. Uzzel T Parthenogenesis in Rep­tiles / Gans C., Billett D. F. (ed.) // Biology of Reptilia. 1985. New York: John Wiley & Sons. – Рp. 413–526.
34. Davoyan A. Study of morphological and genetic variability of parthe­nogenetic rock lizard Darevskia dahli. Yerevan, Armenia // PhD The­sis. 2007. 119 p.
35. Dawley R. M. An introduction to unisexual vertebrates / Dawley R. M., Bogart J. P. (ed.) // Evolution and ecology of unisexual verte­brates. Bull New York State Museum. Albany, New York, 1989. V. 466. Pp. 18.
36. Destabilization of tracts of simple repetitive DNA in yeast by muta­tions affecting DNA mismatch repair / Strand M., Prolla T. A., Liskay R. M. et al. // Nature. 1993. 365. Рр. 274–276.
37. Distribution of dinucleotide microsatellites in the Drosophila melanogaster genome / Bachtrog D., Wegs S., Zangerl B. et al. // Molecular Biology Evolution. 1999. V. 16. Pp. 602−610.
38. Divergence of the cytohrome b gene in the Lacerta raddei complex and its parthenogenetic daughter species: Evidence for recent multiple origins / Fu J., MacCulloch R. D., Murphy R.W. et al. // Copeia.
2000. V. 2. Pр. 432–440.
g 84 G
Ê
ЛОНАЛЬНОЕ РАЗНООБРАЗИЕ И МЕХАНИЗМЫ ЕГО ФОРМИРОВАНИЯ У ЯЩЕРИЦ РОДА
Darevskia
39. Effect of tandemly repeated AGG triplets on the translation of CAT­mRNA in E. coli. / Ivanov I., Alexandrova R., Dragulev B. et al. // FEBS Letters. 1992. V. 307. Pр. 173–176.
40. Elder J. F., Schlosser I. J. Extreme clonal uniformity of Phoxinus eos/ neogaeus gynogens among variable habitats in northern Minnesota beaver ponds // Proceedings of the National Academy of Sciences USA. 1995. V. 92. Pp. 50015005.
41. Ellegren H. Microsatellite mutations in the germline: implication for evolutionary inference // Trends in genetics. 2000. V. 16. 12. Pp. 551558.
42. Ellegren H. Microsatellites: simple sequences with complex evolu­tion // Nat Rev Genet. 2004. 5. Р. 435–445.
43. Engeler B., Reyer H. U. Choosy females and indiscriminative males: mate choice in mixed populations of sexual and hybridogenetic water frogs (Rana lessonae, Rana esculenta) // Behavioral Ecology. 2001. V. 12. Pp. 600606.
44. Enhanced gene expression by the poly (dT-dG)-poly (dC-dA) se­quence / Hamada H., Seidman M., Howard B. H. et al. // Molecular and Cellular Biology. 1984. V.4 . Pр. 2622–2630.
45. Evidence for a connection between the mismatch repair system and the G2 cell cycle checkpoint / Hawn M. T., Umar A., Carethers J. M. et al. // Cancer Research. 1995. V. 55. Pр. 3721–3725.
46. Extensive somatic microsatellite mutations in normal human tissue / Vilkki S., Loukola A., Poyhonen M. et al. // Cancer Research. 2001. V. 61. Pр. 4541–4544.
47. Fitness loss and germline mutations in barn swallows breeding in Chernobyl / Ellegren H., Lindgren G., Primmer C. R. et al. // Nature.
1997. V. 389. Pp. 593596.
48. Fu J., MacCulloch R. D, Murphy R. W. The parthenogenetic Rock Lizard Lacerta unisexualis: An Example of Limited Genetic Polymor­phism // Journal of Molecular Evolution. 1998. V. 46. Pр. 127–130.
49. Gendrel C. G., Boulet A., Dutreix M. (CA/GT)
microsatellites affect
n
homologous recombination during yeast meiosis // Genes & Develop­ment. 2000. V. 14. Pр. 1261–1268.
50. Genetic diversity and the dynamics of hybrid parthenogenesis in Cne- midophorus (Teiidae) and Heteronotia (Gekkonidae) / Moritz C., Brown W. M., Densmore L. D. et al. // Dawley R. M, Bogart J. P. (eds.). Evolution and Ecology of Unisexual vertebrates. Albany, N.Y. // New York State Museum Bulletin. 1989. 466. Pp. 87−112.
51. Genetic variation and de novo mutations in the parthenogenetic Cau­casian rock lizard Darevskia unisexualis / Badaeva T. N., Malysheva D. N., Korchagin V. I. et al. // PLoS ONE. 2008; 3(7): e2730. doi:10.1371/journal.pone.0002730.
g 85 G
À.À. Â
ЕРГУН
, À.Å. Ã
ИРНЫК
, Ô.À. Î
СИПОВ
, À.Â. Î
МЕЛЬЧЕНКО
52. Genetic variation in clonal vertebrates detected by simple sequence DNA fingerprinting / Turner B. J., Elder J. F., Laughlin T. H. et al. // Proceedings of the National Academy of Sciences USA. 1990. V. 87. Pр. 56535657.
53. Genetic variation in parthenogenetic Caucasian rock lizards of the genus Lacerta (L. dahli, L. armeniaca, L. unisexualis) analyzed by DNA fingerprinting / Tokarskaya O. N., Kan N. G., Petrosyan V. G. et al. // Molecular Genetics and Genomics. 2001. V. 265. Pр. 812819.
54. Genome composition and tandemly repetitive sequence at some cen­tromers in the lizard Podarcis s. sicula Raf / Capriglione Т., Olmo E., Odierna G. et al. // Genetica. 1989. V. 79. Pp. 8591.
55. Genomic variation in parthenogenetic lizard Darevskia armeniaca: evidence from DNA fingerprinting data / Malysheva D. N., Tokar­skaya O. N., Petrosyan V. G. et al. // Journal of Heredity. 2007. V. 98. 2. Рp. 173178.
56. Goldstein D. B., Pollock D. D. Launching microsatellites: a review of mutation processes and methods of phylogenetic inference // Journal of Heredity. 1997. V. 88. Pр. 335–342.
57. Gordenin D. A., Kunkel T. A., Resnick M. A. Repeat expansion – all in a flap? // Nature Genetics. 1997. 16. Рр. 24–33.
58. Graf J-D and Muller W. P. Experimental gynogenesis provides evi­dence of hybridogenetic reproduction in the Rana esculenta com­plex // Experimentia. 1979. V. 35. Pр. 1574–1576.
59. Harrington R.W. Oviparous hermaphroditic fish with internal fertiliza­tion // Science. 1961. V. 134. Pр. 17491750.
60. Hedrick P. W. Highly variable loci and their interpretation in evolution and conservation // Evolution. 1999. V. 53. . 2. Pр. 313318.
61. Herpetofauna of Armenia and Nagoro-Karabakh / Arakelyan M. S., Danielyan F. D., Corti C. et al. // Salt Lake City: Society for Study of Amphibians and Reptiles, 2011. Pp.154.
62. Highly conserved repetitive DNA sequences are present at human centro­meres / Grady D. L., Ratliff R. L., McCanlies E. C. et al. // Proceedings of National Academy of Sciences USA. 1992. V. 89. Pр. 16951699.
63. Hubbs C., Drewry G., Warburton B. Occurrence and Morphology of a Phenotypic Male of a Gynogenetic Fish // Science. 1959. V. 129. . 3357. Pр. 12271229.
64. Instability of (GATA) sian rock lizard Darevskia unisexualis (Lacertidae) / Tokarskaya O. N., Martirosyan I. A., Badaeva T. N. et al. // Molecular Genetics and Genomics. 2004. V. 270. Pр. 509513.
65. Internal fertilization in an oviparous frog (Eleutherodactylus coqui) / Townsend D. S., Stewart M. M., Pough F. H. et al. // Science. 1981. V. 212. P. 469471.
microsatellite loci in parthenogenetic Cauca-
n
g 86 G
Ê
ЛОНАЛЬНОЕ РАЗНООБРАЗИЕ И МЕХАНИЗМЫ ЕГО ФОРМИРОВАНИЯ У ЯЩЕРИЦ РОДА
Darevskia
66. Jeffreys A. J., Wilson V., Tein S. L. Hypervariable minisatellite regions in human DNA // Nature. 1985. V. 314. Pр. 6773.
67. Kelly R. G. Similar origins of two mouse minisatellites within transpo­son-like LTRs // Genomics. 1994. V. 24. Pp. 509–515.
68. Koreth J., O’leary J. J., McGee J. O. D. Microsatellites and PCR ge­nomic analysis // Journal of Pathology. 1996. V. 178. Pp. 239248.
69. Kupriyanova L. A. Additional chromosomes of Mabuya aurata sep- temtaeniata lizard // Tsitologiya i Genetika. 1974. № 16(12). Рр. 15191521.
70. Laboratory synthesis of an independently reproducing vertebrate spe­cies / Lutes A. A., Baumann D. P., Neaves W. B. et al. // PNAS.
2011. V. 108. 24. Pp. 9910–9915.
71. Li Q., Hisatsune T., Kijima A. Induction of haploid androgenesis in Pacific oyster by UV irradiation // Marine Biotechnology (New York).
2004. V. 6. . 3. Pp. 291297.
72. Lima N. R. W., Koback C. J., Vrijenhoek R. C. Evolution of sexual mim­icry in sperm-dependent clonal forms of Poeciliopsis (Pisces: Poecilii­dae) // Journal of Evolutionary Biology. 1996. V. 9. Pp. 185203.
73. Lyapunova E. A., Ahverdyan M. R., Vorontsov N. N. Robertson’s fan of variability of chromosome in Caucasian subalpic field-vole (Pitymys, Microtinae, Rodentia) // Russ J Genet. 1988. 9(2). Pp. 480483.
74. Macgregor H. C., Uzzell T. M. Gynogenesis in salamanders related to Ambystoma jeffersonianum // Science. 1964. V. 143. N. 3. Pp. 10431045.
75. Marescalchi O., Scali V. Automictic parthenogenesis in the diploid­triploid stick insect Bacillus atticus and its flexibility leading to het­erospecific diploid hybrids // Invertebrate Reproduction and Devel­opment. 2003. V. 43. Pp. 163–172.
76. Microsatellites: genomic distribution, putative functions and muta­tional mechanisms: a review / Li Y. C., Korol A. B., Fahima T. et al. // Molecular Ecology. 2002. V. 11. Pp. 2453 –2465.
77. Microsatellite mutations in litters of the Australian lizard Egernia stokesii / Gardner M. G., Bull C. M., Cooper S. J. B. et al. // Journal of Molecular Biology. 2000. V. 13. Pр. 551−560.
78. Molecular characterization of allelic variants of (GATA)
microsatellite
n
loci in parthenogenetic lizards Darevskia unisexualis (Lacertidae) / Korchagin V. I., Badaeva T. N., Tokarskaya O. N. et al. // Gene. 2007. V. 392. Pp. 126133.
79. Morishima K., Yoshikawa H., Arai K. Meiotic hybridogenesis in trip­loid Misgurnus loach derived from a clonal lineage // Heredity. 2008. Pp. 100, 581–586.
g 87 G
À.À. Â
ЕРГУН
, À.Å. Ã
ИРНЫК
, Ô.À. Î
СИПОВ
, À.Â. Î
МЕЛЬЧЕНКО
80. Moritz C., Wright J. W., Brown C. M. Mitochondrial DNA analysis and the origin and relative age of parthenogenetic Cnemidophorus: phylogenetic constraints on hybrid origins // Evolution. 1992. 46. Pp. 184–192.
81. Mutational processes of simple sequence repeat loci in human popula­tions / Di Rienzo A., Peterson A. C., Garza J. C. et al. // Proceedings of National Academy of Sciences USA. 1994. 91. Рp. 3166–3170.
82. Mutation rate varies among alleles at a microsatellite locus: Phyloge­netic evidence / Jin L., Macaubas C., Hallmayer J. et al. // Proceed­ings of the National Academy of Sciences USA. 1996. V. 93. Pр. 1528515288.
83. Natural clones detected by multilocus DNA fingerprinting in gynoge­netic triploid ginbuna Carassius langsdorfii in the Kurose River, Hi­roshima / Umino T., Arai K., Maeda K. et al. // Fisheries Science.
1997. V. 63. Pр. 147148.
84. Nur U. Mitotically unstable supernumerary chromosomes with an ac­cumulation mechanism in a grasshopper // Chromosoma. 1963. V. 14. Pp. 407–422.
85. Ohta T., Kimura M. The model of mutation appropriate to calculate the number of electrophoretically detectable alleles in a genetic popu­lation // Genetics Research. 1973. 22. P. 201.
86. Olde age, multiple formations or genetic plasticity? Clonal diversity in the uniparental Caucasian rock lizard, Lacerta dahli / Murphy R. W., Darevsky I. S., MacCulloch R. D. et al. // Genetica. 1997. 101. Pp. 125−130.
87. Olmo E. Genome Variations in the transition from Amphibians to Reptiles // Journal of Molecular Evolution. 1991. V. 33. P. 6875.
88. Olmo E., Odierna G., Capriglione T. The karyology of mediterranean Lacertidae lizards / Eds: Valakos E. D., Böhme W., Perez-Mellado V., Maragou P., Athens, Bonn, Alicante // Lacertid of the mediterranean region. 1993. Pp. 6184.
89. Olsen M. W. Performance record of a parthenogenetic turkey male // Science. 1960. V. 132. . 3440. Pp. 1661.
90. On the essence of 'meaningless' simple repetitive DNA in eukaryote genomes / Epplen C., Melmer G., Siedlaczck I. et al. // DNA Finger­printing: State of the Science (eds: Pena S. D. J., Chakraborty R., Ep­plen J. T., Jeffreys A. J. ). 1993. Pр. 29–45.
91. On the stability of dispensable constituents of the eukaryotic genome: Stability of coding sequences versus truly hypervariable sequences in a clonal vertebrate, the amazon molly, Poecilia Formosa / Schartl M., Schlupp I., Schartl A. et al. // Proceedings of the National Academy of Sciences USA. 1991. V. 88. Pp. 8759 – 8763.
g 88 G
Ê
ЛОНАЛЬНОЕ РАЗНООБРАЗИЕ И МЕХАНИЗМЫ ЕГО ФОРМИРОВАНИЯ У ЯЩЕРИЦ РОДА
Darevskia
92. Osipov F., Vergun A., Ryskov A. Clonal variation in the parthenoge­netic lizard species Darevskia rostombekowi (Lacertidae) // Book of Abstracts of 9th Symposium on the Lacertids of the Mediterranean Basin & 1st Symposium on Mediterranean Lizards. Lemesos (Limassol), Cyprus. 2023 June 2016. P. 29.
93. Parker E. D., Walker J. M, Paulissen M. A. Clonal diversity in Cnemi- dophorus: ecological and morphological consequences / Dawley R. M, Bogart J. P. (ed.). Evolution and Ecology of Unisexual vertebrates. Albany, N.Y // New York State Museum Bulletin. 1989. № 466. Pp. 72−86.
94. Pearson C. E., Sinden R. R. Alternative structures in duplex DNA formed within the trinucleotide repeats of the myotonic dystrophy and fragile X loci // Biochemistry. 1996. 35. Pp. 5041–5053.
95. Porter K. R. Androgenetic development of the egg of Rana pipiens // Biological Bulletin. 1939. V. 77. P.233257.
96. Purdom C. E. Genetics and fish breeding / Chapman, Hall. // Fish and Fisheries Series. United Kingdom, London, 1993. 8. P. 291.
97. Restriction endonuclease analysis of highly repetitive DNA as a phy­logenetic tool / Grechko V. V., Fedorova L. V., Slobodyanyuk S. Ya. et al. // Journal of Molecular Evolution. 1997. V. 45. 3. Pр. 332336.
98. Ryskov A. P. Genetically unstable microsatellite-containing loci and genome diversity in clonally reproduced unisexual vertebrates / Ed: Kwang Jeon // International Review of Cell and Molecular Biology. – Elsevier, Academic Press (USA), 2008. V. 270. Pp. 319349.
99. Sister Chromosome Pairing Maintains Heterozygosity in Parthenoge­netic Lizards / Lutes A. A., Neaves W. B., Baumann D. P. et al. // Nature. 2010. 464(7286). Pp. 283–286.
100. Schafer R., Zischler H., Epplen J. T. (CAC)
, a very informative oli-
5
gonucleotide probe for DNA fingerprinting // Nucleic Acids Re­search. 1988. V. 16. . 11. Pp. 5196.
101. Schlötterer C., Tautz D. Slippage synthesis of simple sequence
DNA // Nucleic Acids Research. 1992. V. 20. Pp. 211215.
102. Spruell P., Thorgaard G.H. Sine sequences detect DNA fingerprints
in salmonid fishes // Heredity. 1996. V. 17. Pp. 317–324.
103. Suomalainen E., Saura A., Lokki J. Polyploidy in association with
parthenogenesis // Cytology and Evolution in Parthenogenesis. Eds: Suomalainen E., Saura A., Lokki J. // CRC Press, Boca Raton. Flor­ida. 1987. P. 71–112.
104. The dynamics of genome evolution and species differentiation / Do-
ver G. A., Brown S., Coen E. et al.; Eds: Dover G. A., Flavel R. B. // Genome evolution. L.: Acad. Press, 1982. Pp. 351−367.
g 89 G
À.À. Â
ЕРГУН
, À.Å. Ã
ИРНЫК
, Ô.À. Î
СИПОВ
, À.Â. Î
МЕЛЬЧЕНКО
105. The effect of mismatch repair deficiency on tumourigenesis; microsa-
tellite instability affecting genes containing short repeated sequences / Johannsdottir J. T., Jonasson J. G., Bergthorsson J. T. et al. // Inter­national Journal of Oncology. 2000. V. 16. Pp.133–139.
106. The Caucasian rock lizard Lacerta rostombekovi: a monoclonal
parthenogenetic vertebrate / MacCulloch R. D., Murphy R. W., Ku­priyanova L. A. et al. // Biochem Syst Ecol. 1997. 25. Pp. 33–37.
107. The origin and evolution of parthenogenesis in Heteronotia binoei
(Gekkonidae): Extensive genotypic diversity among parthenogens / Moritz C., Donnelan S., Adams M. et al. // Evolution. 1989. 43. Pp. 994–1003.
108. The maternal ancestry and approximate age of parthenogenetic spe-
cies of Caucasian rock lizards (Lacerta: Lacertidae) / Moritz C., Uzzel Т., Spolsky C. et al. // Genetica. 1992. 87. Pp. 5362.
109. Toth G., Gaspan Z., Jurka J. Microsatellites in different eukaryotic
genomes survey and analysis // Genome Research. 2000. V. 10. Pр. 967981.
110. Two dispersed highly repeated DNA families of Truturus vulgaris
meridionales (Amphibia, Urodela) are widely conserved among Sala­mandridae / Vignali R., Rijili F. M., Batistoni R. et al. // Chromo­soma. 1991. V. 100. Pр. 8796.
111. Unisexual salamanders (genus Ambystoma) present a new reproduc-
tive mode for eukaryotes / Bogart J. P., Bi K., Fu J. et al. // Genome.
2007. 50. Рp. 119–136.
112. Uzzell Т. М., Darevsky I. S. Biochemical evidence for the hybrid ori-
gin of the parthenogenetic species of the Lacerta saxicola complex (Sauria: Lacertidae), with a discussion of some ecological and evolu­tionary implications // Copeia. 1975. V. 2. Pр. 204222.
113. Uzzell T. M. Meiosis mechanisms of naturally occurring unisexual
vertebrates // American Nature. 1970. V. 104. Pр. 433445.
114. Valdes A. M., Slatkin M., Freimer N. B. Allele frequencies at mi-
crosatellite loci: the stepwise mutation model revisited // Genetics.
1993. V.133. P.737–749.
115. Varley J. M., Macgregor H. C., Barnett L. Characterisation of a short,
highly repeated and centromerically localised DNA sequence in crested and marbled newts of the genus Triturus // Chromosoma.
1990. V. 100. . 1. P. 1531.
116. Wang Weber J. L., Wong C.
peats // Human Molecular Genetic. 1993. 2. Рр. 1123–1128.
117. Wells R. D. Molecular basis of genetic instability of triplet repeats //
Journal of Biological Chemistry. 1996. 271(6). Рр. 2875–2878.
118. Wolfgang S., Cho S. Possible role of natural selection in the formation
of Tanden-Repetitive noncoding DNA // Genetics. 1994. V. 136. Pр. 333341.
Mutation of human short tandem re-
g 90 G
Соседние файлы в предмете [НЕСОРТИРОВАННОЕ]