Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Synapsis and recombination of autosomes and sex chromosomes in two terns (Sternidae, Charadriiformes, Aves). / Lisachov, A. P.; Malinovskaya, L. P.; Druzyaka, A. V. и др.
в: Вавиловский журнал генетики и селекции, Том 21, № 2, 2017, стр. 259-268.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Synapsis and recombination of autosomes and sex chromosomes in two terns (Sternidae, Charadriiformes, Aves)
AU - Lisachov, A. P.
AU - Malinovskaya, L. P.
AU - Druzyaka, A. V.
AU - Borodin, P. M.
AU - Torgasheva, A. A.
N1 - Publisher Copyright: © AUTHORS, 2017.
PY - 2017
Y1 - 2017
N2 - The frequency of recombination and the patterns of crossover site distribution along the chromosomes vary considerably among animal species, including closely related species. Several hypotheses concerning the adaptive value and evolution of these variations were proposed. It was supposed that the recombination patterns of the species' genomes are influenced by their phylogenetic history and ecology. However, most original data were obtained from mammals. The mammals show high karyological variability, which strongly influences the recombination patterns. Therefore it is important to study recombination rate and distribution in more karyologically stable taxa, such as reptiles and birds. We used immunolocalization of SYCP3, the protein of the lateral element of the synaptonemal complex (SC), centromere proteins and the mismatch-repair protein MLH1, which is associated with the recombination nodules, at the synaptonemal complex spreads of prophase oocytes of two tern species, black tern (Chlidonias Niger) and common tern (Sterna hirundo). We first described the karyotype of Ch. Niger (2n=74, FN=94) and identified suggestive rearrangements by which its karyotype differs from that of S. hirundo (2n=68, FN=90). We found that these species significantly differed by the numbers of the MLH1 foci per cell (Ch. Niger: 53.0 ± 4.2; S. hirundo: 44.1 ± 5.0). We showed that the difference in the crossover numbers per cell was determined by the difference in the SC length (total and of individual bivalents) and by chromosomal rearrangements, which also influenced the distributions of crossover sites along the chromosomes. The difference in recombination patterns was higher between the rearranged homeologues than between the non-rearranged ones. We investigated the synaptic patterns of the heteromor-phic Z and W chromosomes, localized the pseudoautosomal regions and estimated their lengths. In spite of several autosomal rearrangements, which differentiate these species, the structure and synaptic patterns of the sex chromosomes have not changed over 9 MY, which have passed since the moment of divergence between the genera Sterna and Chlidonias.
AB - The frequency of recombination and the patterns of crossover site distribution along the chromosomes vary considerably among animal species, including closely related species. Several hypotheses concerning the adaptive value and evolution of these variations were proposed. It was supposed that the recombination patterns of the species' genomes are influenced by their phylogenetic history and ecology. However, most original data were obtained from mammals. The mammals show high karyological variability, which strongly influences the recombination patterns. Therefore it is important to study recombination rate and distribution in more karyologically stable taxa, such as reptiles and birds. We used immunolocalization of SYCP3, the protein of the lateral element of the synaptonemal complex (SC), centromere proteins and the mismatch-repair protein MLH1, which is associated with the recombination nodules, at the synaptonemal complex spreads of prophase oocytes of two tern species, black tern (Chlidonias Niger) and common tern (Sterna hirundo). We first described the karyotype of Ch. Niger (2n=74, FN=94) and identified suggestive rearrangements by which its karyotype differs from that of S. hirundo (2n=68, FN=90). We found that these species significantly differed by the numbers of the MLH1 foci per cell (Ch. Niger: 53.0 ± 4.2; S. hirundo: 44.1 ± 5.0). We showed that the difference in the crossover numbers per cell was determined by the difference in the SC length (total and of individual bivalents) and by chromosomal rearrangements, which also influenced the distributions of crossover sites along the chromosomes. The difference in recombination patterns was higher between the rearranged homeologues than between the non-rearranged ones. We investigated the synaptic patterns of the heteromor-phic Z and W chromosomes, localized the pseudoautosomal regions and estimated their lengths. In spite of several autosomal rearrangements, which differentiate these species, the structure and synaptic patterns of the sex chromosomes have not changed over 9 MY, which have passed since the moment of divergence between the genera Sterna and Chlidonias.
KW - Chromosomal rearrangements
KW - Immunostaining
KW - Meiosis
KW - Sex chromosomes
KW - Sternidae
KW - Synaptonemal complex
UR - http://www.scopus.com/inward/record.url?scp=85023183040&partnerID=8YFLogxK
U2 - 10.18699/VJ17.245
DO - 10.18699/VJ17.245
M3 - Article
AN - SCOPUS:85023183040
VL - 21
SP - 259
EP - 268
JO - Вавиловский журнал генетики и селекции
JF - Вавиловский журнал генетики и селекции
SN - 2500-0462
IS - 2
ER -
ID: 8975511