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Dianat, M.

Publications and source records attributed to Dianat, M..

3 recordsLinked to original sources

Incipient speciation, rapid expansion and repeated introgressive hybridization in an African Giant Shrew (Crocidura olivieri)

The African giant shrew (Crocidura olivieri) is one of the most widespread native small mammals in sub-Saharan Africa, occupying habitats ranging from humid tropical forests to arid Savanna. Its broad distribution, ecological diversity, and unresolved evolutionary relationships suggest a history of rapid diversification, yet the roles of hybridization and demographic expansion remain poorly understood. We combined genome-wide ddRAD and mitochondrial data from populations sampled across sub-Saharan Africa to reconstruct the evolutionary history of African giant shrews. We reveal extensive mitonuclear discordance across the clade and show that it reflects a complex history of repeated introgressive hybridization rather than a single evolutionary event. Genomic analyses resolve three major evolutionary lineages and identify four introgression events, including extensive bidirectional genome-wide introgression between the ancestors of the C. olivieri and arid adapted species followed by later unidirectional introgression associated with range expansion. Within the C. olivieri group, we identify five geographically structured lineages connected by ongoing gene flow, representing different stages of incipient speciation. Demographic analyses further reveal repeated population expansion during the Late Pleistocene and Early Holocene, with lineage-specific timing consistent with climatic fluctuations and a possible contribution of increasing human association. Our results identify repeated range expansion and hybridization as major drivers of diversification in African giant shrews and establish this system as a powerful model for studying the genomic processes underlying early speciation.

evolutionary biology↗

DNA methylation profile is not inherited in offspring of a short-lived annual fish

Parental ageing can influence offspring through non-genetic mechanisms. The contribution of epigenetic inheritance parental effects still remains poorly understood. DNA methylation is a widespread regulator of gene expression that changes during development and ageing and can also act as a mediator of intergenerational effects. We tested whether age-related changes in parental DNA methylation are transmitted to offspring in the short-lived turquoise killifish (Nothobranchius furzeri, Cyprinodontiformes). Using reduced-representation sequencing, we quantified genome-wide DNA methylation and examined methylation dynamics at individual loci. The overall proportion of methylated CpG sites increased during early ageing but declined at later ages, revealing a non-linear trajectory with substantial among-individual variation. Despite these age-related changes, we found no evidence that parental methylation patterns were transmitted to offspring, either at the genome-wide level or at individual loci. Our findings indicate that although DNA methylation undergoes pronounced age-dependent remodelling in adult killifish, these changes are not detectably inherited by the next generation. We discuss these results in the context of epigenetic inheritance and ageing in vertebrate model systems.

evolutionary biology↗

Fins as a reliable surrogate tissue for age-related changes of telomeres and DNA methylation in gonads of a short-lived fish

Senescence is a multifactorial and individualised process of age-related physiological decline. Cellular markers, such as telomere length and DNA methylation, can reveal subtle changes associated with chronological age or expected lifespan. In this study, we evaluated the utility of fin tissue as a surrogate for assessing telomere length and proportion of DNA methylation in the gonads of a small, short-lived laboratory fish, the turquoise killifish (Nothobranchius furzeri). We collected fin and gonadal tissues from both females and males at three different ages, and extracted DNA to measure telomere length via terminal restriction fragment (TRF) analysis and global DNA methylation levels using double-digest restriction-associated DNA sequencing (ddRADseq). Our results show a notable correspondence between telomere length and DNA methylation patterns in fin and gonadal tissues. These findings support the use of fin biopsies as a non-lethal method for assessing ageing biomarkers in the gonads of small freshwater fish.

molecular biology↗