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PMID: 2461587 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Activation of developmentally mutated human globin genes by cell fusion.

Science (New York, N.Y.) ·Vol. 242 ·No. 4881 ·1988-11-18 ·Pages 1056-8

Papayannopoulou T, Enver T, Takegawa S, Anagnou NP, Stamatoyannopoulos G

Abstract

Human fetal globin genes are not expressed in hybrid cells produced by the fusion of normal human lymphocytes with mouse erythroleukemia cells. In contrast, when lymphocytes from persons with globin gene developmental mutations (hereditary persistence of fetal hemoglobin) are used for these fusions, fetal globin is expressed in the hybrid cells. Thus, mutations of developmental origin can be reconstituted in vitro by fusing mutant lymphoid cells with differentiated cell lines of the proper lineage. This system can readily be used for analyses, such as globin gene methylation, that normally require large numbers of pure nucleated erythroid cells, which are difficult to obtain.

MeSH Terms
Animals Cell Fusion Chromosome Deletion Fetal Hemoglobin/genetics Gene Expression Regulation Globins/genetics Hemoglobinopathies/genetics Humans Leukemia, Erythroblastic, Acute Mice Mutation Promoter Regions, Genetic RNA, Messenger/genetics
Chemicals
RNA, Messenger Globins Fetal Hemoglobin
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Papayannopoulou T
Division of Hematology, University of Washington, Seattle 98195.
Enver T
Takegawa S
Anagnou N P
Stamatoyannopoulos G
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1988-11-18
Pages
1056-8
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIDDK NIH HHS · DK30852 · United States
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