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Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes

Abstract

Williams syndrome (WS) is a contiguous gene deletion disorder caused by haploinsufficiency of genes at 7q11.23 . We have shown that hemizygosity of elastin is responsible for one feature of WS, supravalvular aortic stenosis (SVAS). We have also implicated LIM-kinase 1 hemizygosity as a contributing factor to impaired visual-spatial constructive cognition in WS. However, the common WS deletion region has not been completely characterized, and genes for additional features of WS, including mental retardation, infantile hypercalcemia, and unique personality profile, are yet to be discovered. Here, we present a physical map encompassing 1.5 Mb DNA that is commonly deleted in individuals with WS. Fluorescence in situ hybridization analysis of 200 WS individuals shows that WS individuals have the consistent deletion interval. In addition, we identify three novel genes from the common deletion region: WS-βTRP, WS-bHLH, and BCL7B. WS-βTRP has four putative β-transducin (WD40) repeats, and WS-bHLH is a novel basic helix-loop-helix leucine zipper (bHLHZip) gene. BCL7B belongs to a novel family of highly conserved genes. We describe the expression profile and genomic structure for each of these genes. Hemizygous deletion of one or more of these genes may contribute to developmental defects in WS.

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Received: 29 June 1998 / Accepted: 3 September 1998

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Meng, X., Lu, X., Li, Z. et al. Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes. Hum Genet 103, 590–599 (1998). https://doi.org/10.1007/s004390050874

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Keywords

  • Aortic Stenosis
  • Hypercalcemia
  • Williams Syndrome
  • Leucine Zipper
  • Personality Profile