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A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndrome
  1. Eva Klopocki (eva.klopocki{at}charite.de)
  1. Institut für Medizinische Genetik, Universitätsmedizin Berlin Charité, Berlin, Germany
    1. Claus-Eric Ott (claus-eric.ott{at}charite.de)
    1. Institut für Medizinische Genetik, Universitätsmedizin Berlin Charité, Berlin, Germany
      1. Niels Benatar (n.benatar{at}marienstift-braunschweig.de)
      1. Klinik für Handchirurgie und angeborene Handfehlbildungen, Krankenhaus Marienstift, Braunschweig, Germany
        1. Reinhard Ullmann (ullmann{at}molgen.mpg.de)
        1. Max-Planck-Institut für Molekulare Genetik, Berlin, Germany
          1. Stefan Mundlos (stefan.mundlos{at}charite.de)
          1. Institut für Medizinische Genetik, Universitätsmedizin Berlin Charité, Berlin, Germany
            1. Katarina Lehmann (katarina.lehmann{at}charite.de)
            1. Universitätsmedizin Berlin, Charité, Germany

              Abstract

              Background: Sonic hedgehog (SHH) plays an important role in defining the anterior-posterior axis in the developing limbs. A highly conserved non-coding sequence about ~ 1 Mb upstream from the sonic hedgehog gene (SHH) was shown to be a long range regulator for SHH expression in the limb bud. Point mutations within this non-coding regulatory region designated ZRS lead to ectopic expression of Shh in the anterior margin of the limb bud as shown in mice and cause the human triphalangeal thumb and polysyndactyly (TPT-PS) phenotype. Even though this association is well established, its molecular mechanism remains unclear.

              Methods and results: We investigated a large pedigree with variable TPT-PS. A single nucleotide exchange within the SHH limb regulator sequence was excluded, but locus specific microsatellite marker analyses confirmed a linkage to this region. Subsequently, array CGH was carried out using a submegabase whole human genome tiling path BAC array revealing a microduplication in 7q36.3 in all affected individuals. A duplicated region of 588,819 bp comprising the ZRS was identified by quantitative real-time PCR and direct sequencing.

              Conclusion: A novel microduplication in 7q36.3 results in a similar TPT-PS phenotype as caused by single nucleotide alterations in the ZRS, the limb specific SHH regulatory element. Duplications can be added to the growing list of mechanisms that cause abnormalities of long range transcriptional control.

              • 7q36 microduplication
              • SHH regulation
              • ZRS
              • polysyndactyly
              • triphalangeal thumb

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