Recombination
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UCLA symposia on molecular and cellular biology ; New series //Vol. 47
782 s. : il.
- MeSH
- rekombinace genetická MeSH
- replikace DNA MeSH
- Publikační typ
- kongresy MeSH
- Konspekt
- Biologické vědy
- NLK Obory
- biologie
- embryologie a teratologie
- genetika, lékařská genetika
UCLA Symposia on Molecular and Cellular Biology.New Series,Vol.47.
25,782 s.,obr.,tab.,grafy. : Bibliogr.,rejstřík.
The survival of species depends on their ability to adapt to environmental changes. While organisms are known to activate common transcriptional pathways in response to temperature variations, the impact of temperature on recombination, a key source of genetic variability, remains largely unexplored. Previous studies in model species have shown that the frequency of recombination during meiotic prophase I can be influenced by extreme temperatures. Yet, it remains unclear whether this effect is also conserved in non-model vertebrates. In this study, we investigated the effect of temperature on recombination in the Guibé's ground gecko (Paroedura guibeae), an ectotherm species. We analyzed the formation of double-strand breaks (DSBs) and crossovers (COs) by immunolocalizing the meiotic proteins involved in these processes. Furthermore, we determined the frequency and chromosomal location of COs and the levels of CO interference (COI). Our findings show the presence of hyper-COs spermatocytes in individuals exposed to both high and low temperatures. Notably, this significant increase in COs was associated with a decrease in chromosome axis lengths and elevated levels of meiotic DSBs in later stages of prophase I. In conclusion, our results provide new insights into the effects of environmental temperatures on meiotic recombination in ectothermic species, underscoring the intricate interplay between environmental factors and genetic processes.
- MeSH
- crossing over (genetika) MeSH
- dvouřetězcové zlomy DNA MeSH
- ještěři * genetika MeSH
- meióza genetika MeSH
- profáze meiózy I genetika MeSH
- rekombinace genetická * genetika MeSH
- spermatocyty metabolismus MeSH
- teplota MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Recently, the reticulated giraffe (G. reticulata) was identified as a distinct species, which emphasized the need for intensive research in this interesting animal. To shed light on the meiotic process as a source of biodiversity, we analysed the frequency and distribution of meiotic recombination in 2 reticulated giraffe males. We used immunofluorescence detection of synaptonemal complex protein (SYCP3), meiotic double strand breaks (DSB, marked as RAD51 foci) in leptonema, and crossovers (COs, as MLH1 foci) in pachynema. The mean number of autosomal MLH1 foci per cell (27), which resulted from a single, distally located MLH1 focus observed on most chromosome arms, is one of the lowest among mammalian species analysed so far. The CO/DSB conversion ratio was 0.32. The pseudoautosomal region was localised in the Xq and Yp termini by FISH and showed an MLH1 focus in 83% of the pachytene cells. Chromatin structures corresponding to the nucleolus organiser regions were observed in the pachytene spermatocytes. The results are discussed in the context of known data on meiosis in Cetartiodactyla, depicting that the variation in CO frequency among species of this taxonomic group is mostly associated with their diploid chromosome number.
- MeSH
- fluorescenční protilátková technika MeSH
- hybridizace in situ fluorescenční MeSH
- meióza genetika MeSH
- MutL homolog 1 genetika MeSH
- organizátor jadérka genetika MeSH
- rekombinace genetická * MeSH
- rekombinasa Rad51 genetika MeSH
- synaptonemální komplex genetika MeSH
- žirafy genetika MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
The hypothesis of wide spread reticulate evolution in Tick-Borne Encephalitis virus (TBEV) has recently gained momentum with several publications describing past recombination events involving various TBEV clades. Despite a large body of work, no consensus has yet emerged on TBEV evolutionary dynamics. Understanding the occurrence and frequency of recombination in TBEV bears significant impact on epidemiology, evolution, and vaccination with live vaccines. In this study, we investigated the possibility of detecting recombination events in TBEV by simulating recombinations at several locations on the virus' phylogenetic tree and for different lengths of recombining fragments. We derived estimations of rates of true and false positive for the detection of past recombination events for seven recombination detection algorithms. Our analytical framework can be applied to any investigation dealing with the difficult task of distinguishing genuine recombination signal from background noise. Our results suggest that the problem of false positives associated with low detection P-values in TBEV, is more insidious than generally acknowledged. We reappraised the recombination signals present in the empirical data, and showed that reliable signals could only be obtained in a few cases when highly genetically divergent strains were involved, whereas false positives were common among genetically similar strains. We thus conclude that recombination among wild-type TBEV strains may occur, which has potential implications for vaccination with live vaccines, but that these events are surprisingly rare.
Genetic recombination during meiosis functions to increase genetic diversity, promotes elimination of deleterious alleles, and helps assure proper segregation of chromatids. Mammalian recombination events are concentrated at specialized sites, termed hotspots, whose locations are determined by PRDM9, a zinc finger DNA-binding histone methyltransferase. Prdm9 is highly polymorphic with most alleles activating their own set of hotspots. In populations exhibiting high frequencies of heterozygosity, questions remain about the influences different alleles have in heterozygous individuals where the two variant forms of PRDM9 typically do not activate equivalent populations of hotspots. We now find that, in addition to activating its own hotspots, the presence of one Prdm9 allele can modify the activity of hotspots activated by the other allele. PRDM9 function is also dosage sensitive; Prdm9+/- heterozygous null mice have reduced numbers and less active hotspots and increased numbers of aberrant germ cells. In mice carrying two Prdm9 alleles, there is allelic competition; the stronger Prdm9 allele can partially or entirely suppress chromatin modification and recombination at hotspots of the weaker allele. In cell cultures, PRDM9 protein variants form functional heteromeric complexes which can bind hotspots sequences. When a heteromeric complex binds at a hotspot of one PRDM9 variant, the other PRDM9 variant, which would otherwise not bind, can still methylate hotspot nucleosomes. We propose that in heterozygous individuals the underlying molecular mechanism of allelic suppression results from formation of PRDM9 heteromers, where the DNA binding activity of one protein variant dominantly directs recombination initiation towards its own hotspots, effectively titrating down recombination by the other protein variant. In natural populations with many heterozygous individuals, allelic competition will influence the recombination landscape.
- MeSH
- alely * MeSH
- HEK293 buňky MeSH
- heterozygot MeSH
- histonlysin-N-methyltransferasa genetika MeSH
- histony genetika MeSH
- kompenzace dávky (genetika) MeSH
- lidé MeSH
- lokus kvantitativního znaku MeSH
- myši knockoutované MeSH
- myši MeSH
- poškození DNA MeSH
- rekombinace genetická * MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
