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Differential amplification of the subtelomeric satellite DNA JcSAT1 in the genus Jatropha L. (Euphorbiaceae)

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Abstract

Satellite DNAs (satDNAs) are highly repetitive sequences that occur in virtually all eukaryotic genomes and can undergo rapid copy number and nucleotide sequence variation among relatives. After chromosomal mapping of the satDNA JcSAT1, it was found a large accumulation at subtelomeres of Jatropha curcas (subgenus Curcas), but an absence of these monomers in J. integerrima (subgenus Jatropha). This fact suggests a dynamic scenario for this satellite repeat in Jatropha genomes. Here, we used a multitasking approach (sequence analysis, DNA blotting and chromosomal mapping) to investigate the molecular organization and chromosomal abundance and distribution of JcSAT1 in a broader group of species from the subgenus Jatropha (J. gossypiifolia, J. mollissima, J. podagrica, and J. multifida) in addition to J. curcas, with the aiming of understanding the evolution of this satDNA. Based on the analysis of BAC clone sequences of J. curcas, a large array (~ 30 kb) of 80 homogeneous monomers of JcSAT1 was identified in BAC 23J11. The monomer size was conserved (~ 358 bp) and contained a telomeric motif at the 5’ end. PCR amplification coupled with a Southern blot revealed the presence of JcSAT1-like sequences in all species examined. However, a large set of genome copies was identified only in J. curcas, where a ladder-like pattern with multimers of different sizes was observed. In situ hybridization of BAC 23J11 confirmed the subtelomeric pattern for J. curcas, but showed no signals on chromosomes of species from the subgenus Jatropha. Our data indicate that JcSAT1 is a highly homogeneous satDNA that originated from a region near the telomeres and spread throughout the chromosomal subtermini, possibly due to frequent ectopic recombination between these regions. The abundance of JcSAT1 in the genome of J. curcas suggests that an amplification event occurred either at the base of the subgenus Curcas or at least in this species, although the repeat is shared by all species of the genus studied so far.

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Acknowledgements

We thank Andrea Pedrosa-Harand from the Laboratory of Plant Cytogenetics and Evolution (Department of Botany, UFPE, Recife-PE, Brazil) for providing the chemicals and devices used in our PCR and Southern blot experiments.

Funding

This study was partially funded by the Brazilian National Council for Scientific and Technological Development (CNPq; PDJ 150912/2017-0) and the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001.

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The study was conceived by A.C.B.V., E.V. and T.R. D.A.M provided the plant material. T.R. conducted bioinformatics, PCR and Southern blot experiments, while E.V. and S.S. assisted with BAC DNA isolation. FISH assays were performed by E.V. and J.R.M.F. A.C.B.V., D.A.M. and S.S. contributed to the discussion. T.R. wrote the paper with final approval from all authors.

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Correspondence to Tiago Ribeiro or Ana Christina Brasileiro-Vidal.

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Ribeiro, T., Vasconcelos, E., de Mendonça Filho, J.R. et al. Differential amplification of the subtelomeric satellite DNA JcSAT1 in the genus Jatropha L. (Euphorbiaceae). Genetica 152, 43–49 (2024). https://doi.org/10.1007/s10709-024-00204-5

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  • DOI: https://doi.org/10.1007/s10709-024-00204-5

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