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- W3085706967 abstract "Abstract Genome functioning in hybrids faces inconsistency. This mismatch is manifested clearly in meiosis during chromosome synapsis and recombination. Species with chromosomal variability can be a model for exploring genomic battles with high visibility due to the use of advanced immunocytochemical methods. We studied synaptonemal complexes (SC) and prophase I processes in 44-chromosome intraspecific ( Ellobius tancrei × E. tancrei ) and interspecific ( Ellobius talpinus × E. tancrei ) hybrid mole voles heterozygous for 10 Robertsonian translocations. The same pachytene failures were found for both types of hybrids. In the intraspecific hybrid, the chains were visible in the pachytene stage, then 10 closed SC trivalents formed in the late pachytene and diplotene stage. In the interspecific hybrid, as a rule, SC trivalents composed the SC chains and rarely could form closed configurations. Metacentrics involved with SC trivalents had stretched centromeres in interspecific hybrids. Linkage between neighboring SC trivalents was maintained by stretched centromeric regions of acrocentrics. This centromeric plasticity in structure and dynamics of SC trivalents was found for the first time. We assume that stretched centromeres were a marker of altered nuclear architecture in heterozygotes due to differences in the ancestral chromosomal territories of the parental species. Restructuring of the intranuclear organization and meiotic disturbances can contribute to the sterility of interspecific hybrids, and lead to the reproductive isolation of studied species. Author summary Meiosis is essential for sexual reproduction to produce haploid gametes. Prophase I represents a crucial meiotic stage because key processes such as chromosomal pairing, synapsis and desynapsis, recombination, and transcriptional silencing occur at this time. Alterations in each of these processes can activate meiotic checkpoints and lead to the elimination of meiocytes. Here we have shown that two groups of experimental hybrids, intraspecific and interspecific—which were heterozygous for 10 identical Robertsonian translocations—had pachytene irregularities and reduced recombination. However, intraspecific and interspecific hybrids exhibited different patterns of synaptonemal complex (SC) trivalent behavior. In the former, open SC trivalents comprised SC chains due to heterosynapsis of short arms of acrocentrics in early and mid-pachytene and were then able to form 2–4 and even 7 and 10 closed SC trivalents in the late pachytene and diplotene stages. In the second mole voles, SC trivalents had stretched centromeres of the metacentrics, and chains of SC trivalents were formed due to stretched centromeres of acrocentrics. Such compounds could not lead to the formation of separate closed SC trivalents. The distant ancestral points of chromosome attachment with a nuclear envelope in the heterozygous nuclei probably lead to stretching of SC trivalents and their centromeric regions, which can be regarded as an indicator of the reorganization of the intranuclear chromatin landscape. These abnormalities, which were revealed in in prophase I, contribute to a decrease the fertility of intraspecific mole voles and promote the sterility of interspecific mole voles." @default.
- W3085706967 created "2020-09-21" @default.
- W3085706967 creator A5017193610 @default.
- W3085706967 creator A5017222197 @default.
- W3085706967 creator A5067902935 @default.
- W3085706967 creator A5073559550 @default.
- W3085706967 creator A5075246132 @default.
- W3085706967 date "2020-09-17" @default.
- W3085706967 modified "2023-09-27" @default.
- W3085706967 title "Meiotic nuclear architecture in distinct mole vole hybrids with Robertsonian translocations: chromosome chains, stretched centromeres, and distorted recombination" @default.
- W3085706967 cites W112846145 @default.
- W3085706967 cites W123646701 @default.
- W3085706967 cites W129902228 @default.
- W3085706967 cites W142319277 @default.
- W3085706967 cites W1489009047 @default.
- W3085706967 cites W1491559418 @default.
- W3085706967 cites W1526311449 @default.
- W3085706967 cites W1679571303 @default.
- W3085706967 cites W1826887444 @default.
- W3085706967 cites W186539977 @default.
- W3085706967 cites W187612398 @default.
- W3085706967 cites W1934445300 @default.
- W3085706967 cites W1965195727 @default.
- W3085706967 cites W1965368044 @default.
- W3085706967 cites W1965933247 @default.
- W3085706967 cites W1965966508 @default.
- W3085706967 cites W1967008105 @default.
- W3085706967 cites W1968369626 @default.
- W3085706967 cites W1969138129 @default.
- W3085706967 cites W1972157095 @default.
- W3085706967 cites W1979847948 @default.
- W3085706967 cites W1981770888 @default.
- W3085706967 cites W1983642572 @default.
- W3085706967 cites W1983844625 @default.
- W3085706967 cites W1984895636 @default.
- W3085706967 cites W1996916367 @default.
- W3085706967 cites W1999155341 @default.
- W3085706967 cites W2000983354 @default.
- W3085706967 cites W2001341582 @default.
- W3085706967 cites W2001612496 @default.
- W3085706967 cites W2002878335 @default.
- W3085706967 cites W2011874180 @default.
- W3085706967 cites W2017434003 @default.
- W3085706967 cites W2019457580 @default.
- W3085706967 cites W2020633819 @default.
- W3085706967 cites W2021294944 @default.
- W3085706967 cites W2022484204 @default.
- W3085706967 cites W2030707215 @default.
- W3085706967 cites W2031655127 @default.
- W3085706967 cites W2037255380 @default.
- W3085706967 cites W2037842315 @default.
- W3085706967 cites W2040019088 @default.
- W3085706967 cites W2043937191 @default.
- W3085706967 cites W2045334024 @default.
- W3085706967 cites W2047683703 @default.
- W3085706967 cites W2048376696 @default.
- W3085706967 cites W2049921855 @default.
- W3085706967 cites W2050677841 @default.
- W3085706967 cites W2052668971 @default.
- W3085706967 cites W2054008728 @default.
- W3085706967 cites W2055273296 @default.
- W3085706967 cites W2056369811 @default.
- W3085706967 cites W2056942376 @default.
- W3085706967 cites W2057092823 @default.
- W3085706967 cites W2060228572 @default.
- W3085706967 cites W2060450076 @default.
- W3085706967 cites W2061182429 @default.
- W3085706967 cites W2062952072 @default.
- W3085706967 cites W2064512698 @default.
- W3085706967 cites W2069321209 @default.
- W3085706967 cites W2080615813 @default.
- W3085706967 cites W2094616277 @default.
- W3085706967 cites W2098955066 @default.
- W3085706967 cites W2099312080 @default.
- W3085706967 cites W2100705274 @default.
- W3085706967 cites W2103076523 @default.
- W3085706967 cites W2106879271 @default.
- W3085706967 cites W2107009563 @default.
- W3085706967 cites W2107359881 @default.
- W3085706967 cites W2111408573 @default.
- W3085706967 cites W2120151566 @default.
- W3085706967 cites W2124684088 @default.
- W3085706967 cites W2132979925 @default.
- W3085706967 cites W2133894023 @default.
- W3085706967 cites W2135527005 @default.
- W3085706967 cites W2137683329 @default.
- W3085706967 cites W2138657939 @default.
- W3085706967 cites W2157537668 @default.
- W3085706967 cites W2159479483 @default.
- W3085706967 cites W2163064140 @default.
- W3085706967 cites W2177046257 @default.
- W3085706967 cites W2181533914 @default.
- W3085706967 cites W2185796732 @default.
- W3085706967 cites W2216502324 @default.
- W3085706967 cites W2219149818 @default.
- W3085706967 cites W2224241142 @default.
- W3085706967 cites W2312521344 @default.
- W3085706967 cites W2345350775 @default.
- W3085706967 cites W2345887576 @default.
- W3085706967 cites W2346702349 @default.