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RNA transcripts of the β‐thalassaemia allele IVS‐2–654 C → T: a small amount of normally processed β‐globin mRNA is still produced from the mutant gene
Author(s) -
Huang Shuzhen,
Zeng Fanyi,
Ren Zhaorui,
Lu Zhihong,
Rodgers Griffin P.,
Schechter Alan N.,
Zeng Yitao
Publication year - 1994
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.1994.tb05071.x
Subject(s) - mutant , messenger rna , microbiology and biotechnology , gene , biology , allele , genetics , globin
Summary. IVS‐2–654 C → T is a common Chines β‐thalassaemia mutation. Previous studies report that this mutation resulted in the formation of an abnormally spliced mRNA and the absence of detectable normal β‐globin mRNA, hence the mutation was considered to cause βd́; ‐ thalassaemia. We recently used the method of PCR amplified cDNA copies of circulating erythroid cell mRNA to analyse the mutant gene transcripts and found that this IVS‐2–654 mutation does not abolish normal RNA processing entirely, but that a significant amount (over 15%) of normally processed β‐globin mRNA is produced. Microglobin chain biosynthetic analysis using the HPLC method showed that β‐globin chain was also present in the blood of patients with IVS‐2–654 C → T mutation. Accordingly, this mutant allele leads to a β + ‐thalassaemia. Further, the methodology described in this paper provides a new approach towards the detection of RNA transcripts in β‐thalassaemia and other genetic diseases.