| |
|
|
|
|
|
|
|||
|
M Castle, D O'Neill and A Bank
Department of Genetics and Development, College of Physicians and Surgeons,
Columbia University, New York, NY.
We report enhanced transcription from the human A gamma-globin gene
promoter in nuclear extracts (NE) of erythroleukemia (K562) cells compared
with that in HeLa NE. We do not observe differences in transcription levels
in the two extracts with nonglobin promoter templates. Our findings,
indicating preferential recognition of the globin gene promoter by nuclear
factors in K562 cells, are consistent with results of studies previously
reported by ourselves and others. A novel finding described here is that
the addition of a double-stranded octamer motif oligonucleotide to K562 NE
increases the level of transcription from the A gamma-globin gene promoter,
suggesting a potential role for an octamer motif-binding factor in the
repression of A gamma-globin gene transcription. A cosmid construct
containing extensive human gamma- and beta-globin gene promoter and
structural sequences as well as upstream control sequences also exhibits
higher levels of globin gene transcription in K562 NE than in HeLa NE. Our
demonstration of the feasibility of efficient, globin promoter-specific in
vitro transcription of this complex template offers a novel approach for
the systematic analysis of the effects of putative regulatory factors on
globin gene expression in vitro in the context of a genetic environment
approximating that found in vivo.
This article has been cited by other articles:
| |||||||||||
| Copyright © 1993 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||