Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients Academic Article uri icon

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abstract

  • The b-globin gene LCR is located approximately 6 kb upstream of the embryonic epsilon-globin gene, and is made up of five DNase I hypersensitive sites (HSs), HS 1-5. LCR plays a pivotal role in regulating the expression of downstream epsilon-, (G)gamma-, (A)gamma-, delta-, and beta-globin genes in cis [1]. Deletions removing the LCR and parts of the downstream beta-globin gene cluster in patients have been described [2]. These individuals present with a (gammadeltabeta)0-thalassemia carrier phenotype. We now report two patients with severe sickle cell disease who were compound heterozygous for Hb S mutation and novel LCR deletion. In one case, HS 1-3 were deleted; in the other, HS 1-5 were deleted. In both cases, the b-like globin genes in cis to the LCR deletions were intact. Genotypically, both patients appeared to have sickle cell trait. Coinherited with either LCR deletion, these individuals presented as sickle cell disease patients. The breakpoints of these LCR deletions were defined. These results affirm that HS 2 and 3 are primarily responsible for conferring erythroid specific high-level expression of cis-linked beta-like globin genes. Furthermore, LCR deletions might cause hemolytic disease of newborns.

authors

  • Koenig, Sara C
  • Becirevic, Esmira
  • Hellberg, Miriam SC
  • Li, Michael Y
  • So, Jason CC
  • Hankins, Jane S
  • Ware, Russell E
  • McMahon, Lillian
  • Steinberg, Martin H
  • Luo, Hong-Yuan
  • Chui, David Hing-kwei

publication date

  • September 2009