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Our fluorescence\n                    <jats:italic>in situ<\/jats:italic>\n                    hybridization experiments revealed that all analysed taxa share the presence of Nfu\u2010SatC repeat but with diverse organization and distribution on chromosomes. Nfu\u2010SatC landscape was similar in conspecific populations of\n                    <jats:italic>Nothobranchius guentheri<\/jats:italic>\n                    and\n                    <jats:italic>Nothobranchius melanospilus<\/jats:italic>\n                    but slightly\u2010to\u2010moderately differed between populations of\n                    <jats:italic>Nothobranchius pienaari<\/jats:italic>\n                    , and between closely related\n                    <jats:italic>Nothobranchius kuhntae<\/jats:italic>\n                    and\n                    <jats:italic>Nothobranchius orthonotus<\/jats:italic>\n                    . Inter\u2010individual variability in Nfu\u2010SatC patterns was found in\n                    <jats:italic>N. orthonotus<\/jats:italic>\n                    and\n                    <jats:italic>Nothobranchius krysanovi<\/jats:italic>\n                    . We revealed mostly no sex\u2010linked patterns of studied repetitive DNA distribution. Only in\n                    <jats:italic>Nothobranchius brieni<\/jats:italic>\n                    , possessing multiple sex chromosomes, Nfu\u2010SatC repeat occupied a substantial portion of the neo\u2010Y chromosome, similarly as formerly found in the XY sex chromosome system of turquoise killifish\n                    <jats:italic>N. furzeri<\/jats:italic>\n                    and its sister species\n                    <jats:italic>Nothobranchius kadleci<\/jats:italic>\n                    \u2014representatives not closely related to\n                    <jats:italic>N. brieni<\/jats:italic>\n                    . All studied species further shared patterns of expected telomeric repeats at the ends of all chromosomes and no additional interstitial telomeric sites. In summary, we revealed (i) the presence of conserved satDNA class in\n                    <jats:italic>Nothobranchius<\/jats:italic>\n                    clades (a rare pattern among ray\u2010finned fishes); (ii) independent trajectories of\n                    <jats:italic>Nothobranchius<\/jats:italic>\n                    sex chromosome differentiation, with recurrent and convergent accumulation of Nfu\u2010SatC on the Y chromosome in some species; and (iii) genus\u2010wide shared tendency to loss of telomeric repeats during interchromosomal rearrangements. Collectively, our findings advance our understanding of genome structure, mechanisms of karyotype reshuffling, and sex chromosome differentiation in\n                    <jats:italic>Nothobranchius<\/jats:italic>\n                    killifishes from the genus\u2010wide perspective.\n                  <\/jats:p>","DOI":"10.1111\/jfb.15550","type":"journal-article","created":{"date-parts":[[2023,9,4]],"date-time":"2023-09-04T03:40:23Z","timestamp":1693798823000},"page":"1501-1514","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":8,"title":["Conserved satellite\n                    <scp>DNA<\/scp>\n                    motif and lack of interstitial telomeric sites in highly rearranged African\n                    <i>Nothobranchius<\/i>\n                    killifish 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