| Literature DB >> 12512836 |
Hua-bing Zhang1, De-Pei Liu, Chih-Chuan Liang.
Abstract
The alpha-globin gene cluster is located at the very tip of the short arm of chromosome 16. It produces the alpha-like globins, which is combined with the beta-like globins to form hemoglobin, and its mutants cause alpha-thalassemia, which is one of the most common genetic diseases. Its expression shows a tissue and developmental stage specificity that is balanced with that of the beta-globin gene cluster. In this article, we summarize the research on the control of expression of the alpha-globin gene cluster, mainly with respect to the alpha-major regulatory element (alpha-MRE): HS-40, the tissue-specific and developmental control of its expression, and its chromosomal environment. In summary, the alpha-globin gene cluster is expressed in an open chromosomal environment; HS-40, the 5'-flanking sequence, the transcribed region, and the 3'-flanking sequence interact to fully regulate its expression.Entities:
Mesh:
Substances:
Year: 2002 PMID: 12512836 DOI: 10.1007/bf02982807
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490