
Molecular Phylogenetics and Evolution, Год журнала: 2024, Номер unknown, С. 108282 - 108282
Опубликована: Дек. 1, 2024
Язык: Английский
Molecular Phylogenetics and Evolution, Год журнала: 2024, Номер unknown, С. 108282 - 108282
Опубликована: Дек. 1, 2024
Язык: Английский
bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown
Опубликована: Окт. 25, 2024
Abstract In a balanced lethal system, half the reproductive output succumbs. Triturus newts are best-known example. Their chromosome 1 comes in two distinct versions and embryos carrying same version twice experience developmental arrest. Those possessing different survive, suggesting that each carries something uniquely vital. With target capture we obtain over 7,000 nuclear DNA markers across genus all main lineages of Salamandridae (the family to which belongs) investigate evolutionary history Triturus’ versus other chromosomes. Dozens genes completely missing from either one or . Furthermore, unique gene content 1A 1B is remarkably similar species, system evolved before radiated. The tree topology differs rest genome, presumably due pervasive, ancient hybridization between ancestor newt lineages. Our findings accentuate complex nature – ‘bloopergene’ driving evolutionarily enigmatic system.
Язык: Английский
Процитировано
6bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown
Опубликована: Ноя. 1, 2024
Abstract The balanced lethal system found in crested and marbled newts of the genus Triturus presents an intriguing mystery. All adults possess two distinct forms their largest chromosome, resulting 50% offspring inheriting copies one these forms. These homomorphic individuals undergo fatal developmental arrest during embryogenesis. How could such obviously maladaptive trait, destroying half organism’s reproductive output, evolve? We construct a high-density linkage maps for its sister Lissotriton , identifying genes involved system. find that each chromosome 1 is characterized by single massive deletion. Ploidy analysis shows deletion compensated duplication same region on opposite chromosome. This suggests was created suddenly, as result unequal exchange between chromosomes individual. simulate consequences mutation, finding that, if rearranged exert fitness penalty when combined with ancestral version, stable can become fixed within population. Counterintuitively, deleterious nature causes isolation protects them from invasion fitter ancestor. conclude origin effectively instantaneous speciation event, which resulted fixation
Язык: Английский
Процитировано
5Conservation Genetics, Год журнала: 2025, Номер unknown
Опубликована: Фев. 6, 2025
Язык: Английский
Процитировано
0bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown
Опубликована: Окт. 25, 2024
Abstract We introduce multiplex Kompetitive Allele-Specific PCR (mxKASP): a modification of ‘classical’ KASP genotyping that allows zygosity to be determined in diploid organisms. Rather than targeting SNP associated with single marker, mxKASP targets two non-homologous markers. show proof concept by applying the balanced lethal system Triturus newts, which individuals are known possess either: (1) zero copies 1A version chromosome 1 and 1B version; (2) one copy 1B; or (3) 1B. is successful amplifying both marker reaction (if present), allowing inferred. independently confirm our results approach. argue can applied rapidly economically determine zygostity organisms, for large number samples at once.
Язык: Английский
Процитировано
3bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown
Опубликована: Окт. 29, 2024
Abstract High throughput sequencing technologies have become essential in the fields of evolutionary biology and genomics. When dealing with non-model organisms or genomic gigantism, whole genomes is still relatively costly therefore reduced-genome representations are frequently obtained, for instance by ‘target capture’ approaches. While computational tools exist that can handle target capture data identify small-scale variants such as single nucleotide polymorphisms micro-indels, options to large scale structural limited. To meet this need, we introduce PAV-spotter: a tool presence/absence variation (PAV) data. PAV-spotter conducts signal cross-correlation calculation, which distribution read counts per between samples different priori defined classes – e.g. male versus female, diseased healthy compared. We apply test our methodology studying Triturus newts: salamanders gigantic currently lack an annotated reference genome. newts suffer from hereditary disease kills half their offspring during embryogenesis. compare two types embryos, characterized unique deletions, those embryos. Our findings show helps expose variants, even face medium low coverage levels, sample sizes, background noise due mis-mapped reads. be used study underlying supergene systems absence genome assemblies. The code, including further explanation on how use customize it, available through GitHub repository: https://github.com/Wielstra-Lab/PAVspotter .
Язык: Английский
Процитировано
2Molecular Phylogenetics and Evolution, Год журнала: 2024, Номер unknown, С. 108282 - 108282
Опубликована: Дек. 1, 2024
Язык: Английский
Процитировано
0