Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Homogeneously Staining Regions (HSR) in Chromosome 1 of the House Mouse: Synapsis and Recombination at Meiosis. / Torgunakov, Nikita Y.; Kizilova, Elena A.; Karamysheva, Tatyana V. и др.
в: Cytogenetic and Genome Research, Том 161, № 1-2, 05.2021, стр. 14-22.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Homogeneously Staining Regions (HSR) in Chromosome 1 of the House Mouse: Synapsis and Recombination at Meiosis
AU - Torgunakov, Nikita Y.
AU - Kizilova, Elena A.
AU - Karamysheva, Tatyana V.
AU - Malinovskaya, Lyubov P.
AU - Bikchurina, Tatiana I.
AU - Borodin, Pavel M.
N1 - Funding Information: This research was funded by the Russian Foundation for Basic Research, grant #19-04-00021, and by the Ministry of Science and Higher Education of the Russian Federation grants #0324-2019-0042 and #2019-0546 (FSUS-2020-0040). The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results. Publisher Copyright: © 2021 S. Karger AG. All rights reserved. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/5
Y1 - 2021/5
N2 - Amplified sequences constitute a large part of mammalian genomes. A chromosome 1 containing 2 large (up to 50 Mb) homogeneously staining regions (HSRs) separated by a small inverted euchromatic region is present in many natural populations of the house mouse (Mus musculus musculus). The HSRs are composed of a long-range repeat cluster, Sp100-rs, with a repeat length of 100 kb. In order to understand the organization and function of HSRs in meiotic chromosomes, we examined synapsis and recombination in male mice hetero- and homozygous for the HSR-carrying chromosome using FISH with an HSR-specific DNA probe and immunolocalization of the key meiotic proteins. In all homozygous and heterozygous pachytene nuclei, we observed fully synapsed linear homomorphic bivalents 1 marked by the HSR FISH probe. The synaptic adjustment in the heterozygotes was bilateral: the HSR-carrying homolog was shortened and the wild-type homolog was elongated. The adjustment was reversible: desynapsis at diplotene was accompanied by elongation of the HSRs. Immunolocalization of H3K9me2/3 indicated that the HSRs in the meiotic chromosome retained the epigenetic modification typical for C-heterochromatin in somatic cells. MLH1 foci, marking mature recombination nodules, were detected in the proximal HSR band in heterozygotes and in both HSR bands of homozygotes. Unequal crossing over within the long-range repeat cluster can cause variation in size of the HSRs, which has been detected in the natural populations of the house mouse.
AB - Amplified sequences constitute a large part of mammalian genomes. A chromosome 1 containing 2 large (up to 50 Mb) homogeneously staining regions (HSRs) separated by a small inverted euchromatic region is present in many natural populations of the house mouse (Mus musculus musculus). The HSRs are composed of a long-range repeat cluster, Sp100-rs, with a repeat length of 100 kb. In order to understand the organization and function of HSRs in meiotic chromosomes, we examined synapsis and recombination in male mice hetero- and homozygous for the HSR-carrying chromosome using FISH with an HSR-specific DNA probe and immunolocalization of the key meiotic proteins. In all homozygous and heterozygous pachytene nuclei, we observed fully synapsed linear homomorphic bivalents 1 marked by the HSR FISH probe. The synaptic adjustment in the heterozygotes was bilateral: the HSR-carrying homolog was shortened and the wild-type homolog was elongated. The adjustment was reversible: desynapsis at diplotene was accompanied by elongation of the HSRs. Immunolocalization of H3K9me2/3 indicated that the HSRs in the meiotic chromosome retained the epigenetic modification typical for C-heterochromatin in somatic cells. MLH1 foci, marking mature recombination nodules, were detected in the proximal HSR band in heterozygotes and in both HSR bands of homozygotes. Unequal crossing over within the long-range repeat cluster can cause variation in size of the HSRs, which has been detected in the natural populations of the house mouse.
KW - Insertion
KW - Inversion
KW - MLH1
KW - Synaptic adjustment
KW - Synaptonemal complex
KW - Multigene Family
KW - Cell Nucleus/metabolism
KW - Epigenesis, Genetic
KW - Male
KW - Recombination, Genetic
KW - Karyotyping
KW - Female
KW - Chromosome Banding
KW - Mice, Inbred C57BL
KW - In Situ Hybridization, Fluorescence
KW - Chromosome Mapping
KW - Meiosis
KW - DNA/genetics
KW - Homozygote
KW - Animals
KW - Chromosome Aberrations
KW - Heterozygote
KW - Mice
KW - Spermatocytes/cytology
KW - Histones/genetics
UR - http://www.scopus.com/inward/record.url?scp=85102819715&partnerID=8YFLogxK
U2 - 10.1159/000513266
DO - 10.1159/000513266
M3 - Article
C2 - 33725692
AN - SCOPUS:85102819715
VL - 161
SP - 14
EP - 22
JO - Cytogenetic and Genome Research
JF - Cytogenetic and Genome Research
SN - 1424-8581
IS - 1-2
ER -
ID: 28142240