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        "description": "Cite as: \nLeroy T, Anselmetti A, Tilak MK, B\u00e9rard S, Csukonyi L, Gabrielli M, Scornavacca C, Mil\u00e1 B, Th\u00e9baud C and Nabholz B. A bird's white-eye view on neo-sex chromosomeTo cite:  evolution. bioRxiv 505610, ver. 4 peer-reviewed and recommended by PCI Evolutionary Biology (2019). DOI: 10.1101/505610",
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          "name": "Thibault Leroy",
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        "person_or_org": {
          "family_name": "S\u00e9verine B\u00e9rard",
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        "affiliations": [
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            "name": "Laboratoire Evolution et Diversit\u00e9 Biologique (EDB), UMR 5174 CNRS \u2013 Universit\u00e9 Paul Sabatier \u2013 IRD, Toulouse, France"
          }
        ],
        "person_or_org": {
          "family_name": "Ma\u00ebva Gabrielli",
          "name": "Ma\u00ebva Gabrielli",
          "type": "personal"
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      },
      {
        "affiliations": [
          {
            "name": "ISEM, Univ Montpellier, CNRS, IRD, EPHE, Montpellier, France"
          }
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          "family_name": "C\u00e9line Scornavacca",
          "name": "C\u00e9line Scornavacca",
          "type": "personal"
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      },
      {
        "affiliations": [
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            "name": "National  Museum  of  Natural  Sciences   (MNCN),  Spanish  National  Research Council (CSIC), Madrid, Spain"
          }
        ],
        "person_or_org": {
          "family_name": "Borja Mil\u00e1",
          "name": "Borja Mil\u00e1",
          "type": "personal"
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      },
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        "affiliations": [
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        ],
        "person_or_org": {
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          "name": "Christophe Th\u00e9baud",
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            "name": "ISEM, Univ Montpellier, CNRS, IRD, EPHE, Montpellier, France"
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    "description": "<p>Chromosomal organization is relatively stable among avian species, especially with regards to sex chromosomes. Members of the large Sylvioidea clade however have a pair of neo-sex chromosomes which is unique to this clade and originate from a parallel translocation of a region of the ancestral 4A chromosome on both W and Z chromosomes. Here, we took advantage of this unusual event to study the early stages of sex chromosome evolution. To do so, we sequenced a female (ZW) of two Sylvioidea species, a <em>Zosterops borbonicus and a Z. pallidus</em>. Then, we organized the <em>Z. borbonicus</em> scaffolds along chromosomes and annotated genes. Molecular phylogenetic dating under various methods and calibration sets confidently confirmed the recent diversification of the genus <em>Zosterops</em> (1-3.5 million years ago), thus representing one of the most exceptional rates of diversification among vertebrates. We then combined genomic coverage comparisons of five males and seven females, and homology with the zebra finch genome (<em>Taeniopygia guttata</em>) to identify sex chromosome scaffolds, as well as the candidate chromosome breakpoints for the two translocation events. We observed reduced levels of within-species diversity in both translocated regions and, as expected, even more so on the neoW chromosome. In order to compare the rates of molecular evolution in genomic regions of the autosomal-to-sex transitions, we then estimated the ratios of non-synonymous to synonymous polymorphisms (<em>&pi;</em><sub><em>N</em></sub><em>/&pi;</em><sub><em>S</em></sub>) and substitutions (d<sub><em>N</em></sub>/d<sub><em>S</em></sub>). Based on both ratios, no or little contrast between autosomal and Z genes was observed, thus representing a very different outcome than the higher ratios observed at the neoW genes. In addition, we report significant changes in base composition content for translocated regions on the W and Z chromosomes and a large accumulation of transposable elements (TE) on the newly W region. Our results revealed contrasted signals of molecular evolution changes associated to these autosome-to-sex chromosome transitions, with congruent signals of a W chromosome degeneration yet a surprisingly weak support for a fast-Z effect.</p>",
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