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Genomic and cytological analysis of the Y chromosome of Drosophila melanogaster: telomere-derived sequences at internal regions
Authors:José?P.?Abad,Beatriz?de?Pablos,Marta?Agudo,Isabel?Molina,Giovanna?Giovinazzo,Antonia?Martín-Gallardo,Alfredo?Villasante  author-information"  >  author-information__contact u-icon-before"  >  mailto:avillasante@cbm.uam.es"   title="  avillasante@cbm.uam.es"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Centro de Biología Molecular Severo Ochoa (CBMSO), CSIC-UAM, Cantoblanco, 28049 Madrid, Spain;(2) Present address: Centre for Neuroscience, King"rsquo"s College London, London, UK;(3) Present address: Departamento de Biología, UAM, Madrid, Spain;(4) Present address: Centro Nacional de Biotecnología, CSIC, Cantoblanco, Madrid, Spain;(5) Servicio Interdepartamental de Investigación (SIdI), UAM, Madrid, Spain
Abstract:The genomic analysis of heterochromatin is essential for studying chromosome behavior as well as for understanding chromosome evolution. The Y chromosome of Drosophila melanogaster is entirely heterochromatic and the under-representation of this chromosome in genomic libraries together with the difficulty of assembling its sequence has made its study very difficult. Here, we present the construction of bacterial artificial chromosome (BAC) contigs from regions h14, h16 and the centromeric region h18. The analysis of these contigs shows that telomere-derived sequences are present at internal regions. In addition, immunostaining of prometaphase chromosomes with an antibody to the kinetochore-specific protein BubR1 has revealed the presence of this protein in some Y chromosome regions rich in telomere-related sequences. Collectively, our data provide further evidence for the hypothesis that the Drosophila Y chromosomes might have evolved from supernumerary chromosomes.The first two authors contributed equally to this workAntonia Martín-Gallardo died Monday, 23 August 2004, after a long battle with cancerThe GenBank Accession numbers for the sequences reported in this paper are AJ549653–96, AJ549701–2, AJ549725–6, AJ 549737–8, AJ549747–8, AJ549751–2, AJ 586980, AJ781048–58
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