Heterochromatin is not the only place for satDNAs: the high diversity of satDNAs in the euchromatin of the beetle Chrysolina americana (Coleoptera, Chrysomelidae)

The satellitome of the beetle Chrysolina americana Linneo, 1758 has been characterized through chromosomal analysis, genomic sequencing, and bioinformatics tools. C-banding reveals the presence of constitutive heterochromatin blocks enriched in A+T content, primarily located in pericentromeric regio...

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Detalhes bibliográficos
Autores: Rico-Porras, José M, Mora, Pablo, Palomeque, Teresa, Montiel, Eugenia E, C. Cabral-de-Mello, Diogo, Lorite, Pedro
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2024
País:España
Recursos:Universidad de Jaén
Repositório:RUJA. Repositorio Institucional de la Producción Científica de la Universidad de Jaén
OAI Identifier:oai:dnet:ruja________::616a516e1c346bdbff647f7416c10b22
Acesso em linha:https://doi.org/10.3390/genes15040395
https://hdl.handle.net/10953/7637
Access Level:Acceso aberto
Palavra-chave:Chrysomelidae
karyotype
repetitive DNA
satellite DNA
satellitome
fluorescence in situ hybridization
genome evolution
heterochromatin
euchromatin
chromosome in silico mapping
CHRISMAPP
240108 Genética Animal
Descrição
Resumo:The satellitome of the beetle Chrysolina americana Linneo, 1758 has been characterized through chromosomal analysis, genomic sequencing, and bioinformatics tools. C-banding reveals the presence of constitutive heterochromatin blocks enriched in A+T content, primarily located in pericentromeric regions. Furthermore, a comprehensive satellitome analysis unveils the extensive diversity of satellite DNA families within the genome of C. americana. Using fluorescence in situ hybridization techniques and the innovative CHRISMAPP approach, we precisely map the localization of satDNA families on assembled chromosomes, providing insights into their organization and distribution patterns. Among the 165 identified satDNA families, only three of them exhibit a remarkable amplification and accumulation, forming large blocks predominantly in pericentromeric regions. In contrast, the remaining, less abundant satDNA families are dispersed throughout euchromatic regions, challenging the traditional association of satDNA with heterochromatin. Overall, our findings underscore the complexity of repetitive DNA elements in the genome of C. americana and emphasize the need for further exploration to elucidate their functional significance and evolutionary implications.