High levels of intra-strain structural variation in Drosophila simulans X pericentric heterochromatin.
Autor: | Courret C; Department of Biology, University of Rochester, Rochester, NY 14627, USA., Larracuente AM; Department of Biology, University of Rochester, Rochester, NY 14627, USA. |
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Jazyk: | angličtina |
Zdroj: | Genetics [Genetics] 2023 Dec 06; Vol. 225 (4). |
DOI: | 10.1093/genetics/iyad176 |
Abstrakt: | Large genome structural variations can impact genome regulation and integrity. Repeat-rich regions like pericentric heterochromatin are vulnerable to structural rearrangements although we know little about how often these rearrangements occur over evolutionary time. Repetitive genome regions are particularly difficult to study with genomic approaches, as they are missing from most genome assemblies. However, cytogenetic approaches offer a direct way to detect large rearrangements involving pericentric heterochromatin. Here, we use a cytogenetic approach to reveal large structural rearrangements associated with the X pericentromeric region of Drosophila simulans. These rearrangements involve large blocks of satellite DNA-the 500-bp and Rsp-like satellites-which colocalize in the X pericentromeric heterochromatin. We find that this region is polymorphic not only among different strains, but between isolates of the same strain from different labs, and even within individual isolates. On the one hand, our observations raise questions regarding the potential impact of such variation at the phenotypic level and our ability to control for such genetic variability. On the other hand, this highlights the very rapid turnover of the pericentric heterochromatin most likely associated with genomic instability of the X pericentromere. It represents a unique opportunity to study the dynamics of pericentric heterochromatin, the evolution of associated satellites on a very short time scale, and to better understand how structural variation arises. Competing Interests: Conflicts of interest The author(s) declare no conflict of interest. (© The Author(s) 2023. Published by Oxford University Press on behalf of The Genetics Society of America.) |
Databáze: | MEDLINE |
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