Variants of a major DNA satellite discriminate parental subgenomes in a hybrid parthenogenetic lizard Darevskia unisexualis (Darevsky, 1966)

Author:

Nikitin Pavel12ORCID,Sidorov Sviatoslav3ORCID,Liehr Thomas4ORCID,Klimina Ksenia5ORCID,Al‐Rikabi Ahmed4ORCID,Korchagin Vitaly6ORCID,Kolomiets Oxana7ORCID,Arakelyan Marine8ORCID,Spangenberg Victor7ORCID

Affiliation:

1. Laboratory of Comparative Ethology and Biocommunication Severtsov Institute of Ecology and Evolution RAS Moscow Russia

2. Faculty of Bioengineering and Bioinformatics Lomonosov Moscow State University Moscow Russia

3. Computational Regulatory Genomics MRC Laboratory of Medical Sciences, Hammersmith Hospital Campus London UK

4. Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics Jena Germany

5. Lopukhin Federal Research and Clinical Center of Physical‐Chemical Medicine of Federal Medical Biological Agency Moscow Russia

6. Institute of Gene Biology RAS Moscow Russia

7. Laboratory of Cytogenetics Vavilov Institute of General Genetics RAS Moscow Russia

8. Department of Zoology Yerevan State University Yerevan Armenia

Abstract

AbstractHybrid parthenogenetic animals are an exceptionally interesting model for studying the mechanisms and evolution of sexual and asexual reproduction. A diploid parthenogenetic lizard Darevskia unisexualis is a result of an ancestral cross between a maternal species Darevskia raddei nairensis and a paternal species Darevskia valentini and presents a unique opportunity for a cytogenetic and computational analysis of a hybrid karyotype. Our previous results demonstrated a significant divergence between the pericentromeric DNA sequences of the parental Darevskia species; however, an in‐depth comparative study of their pericentromeres is still lacking. Here, using target sequencing of microdissected pericentromeric regions, we reveal and compare the repertoires of the pericentromeric tandem repeats of the parental Darevskia lizards. We found species‐specific sequences of the major pericentromeric tandem repeat CLsat, which allowed computational prediction and experimental validation of fluorescent DNA probes discriminating parental chromosomes within the hybrid karyotype of D. unisexualis. Moreover, we have implemented a generalizable computational method, based on the optimization of the Levenshtein distance between tandem repeat monomers, for finding species‐specific fluorescent probes for pericentromere staining. In total, we anticipate that our comparative analysis of Darevskia pericentromeric repeats, the species‐specific fluorescent probes that we found and the pipeline that we developed will form a basis for the future detailed cytogenomic studies of a wide range of natural and laboratory hybrids.

Publisher

Wiley

Reference56 articles.

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