Human alpha- and beta-globin gene transcription in mouse erythroleukaemia cells

Philos Trans R Soc Lond B Biol Sci. 1984 Dec 4;307(1132):261-70. doi: 10.1098/rstb.1984.0126.

Abstract

Human beta-globin genes introduced into mouse erythroleukaemia (MEL) cells by DNA co-transformation are correctly regulated when erythroid cell differentiation is induced by dimethylsulphoxide (DMSO). In contrast, cloned human alpha-globin genes are efficiently transcribed in MEL cells before induction, and no increase in the level alpha-globin mRNA is observed when the cells differentiate. These observations suggest that the mechanisms by which alpha- and beta-globin genes are activated during erythroid cell differentiation are fundamentally different. Analysis of the transcription of hybrid human alpha-beta-globin genes in MEL cells revealed that the sequences responsible for differences in transcription of the intact alpha- and beta-globin genes are located on the 3' side of the mRNA capping site of the two genes, suggesting that cis-acting regulatory sequences are located within the structural genes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Cell Differentiation / drug effects
  • Cell Line
  • DNA Restriction Enzymes
  • Dimethyl Sulfoxide / pharmacology
  • Genes*
  • Globins / genetics*
  • Humans
  • Leukemia, Erythroblastic, Acute / metabolism*
  • Leukemia, Erythroblastic, Acute / pathology
  • Leukemia, Experimental / metabolism*
  • Leukemia, Experimental / pathology
  • Mice
  • Plasmids
  • Transcription, Genetic*
  • Transformation, Genetic

Substances

  • Globins
  • DNA Restriction Enzymes
  • Dimethyl Sulfoxide