共 39 条
Initiation of DNA replication at the human β-globin 3′ enhancer
被引:9
作者:
Buzina, A
Aladjem, MI
Kolman, JL
Wahl, GM
Ellis, J
机构:
[1] Hosp Sick Children, Dev Biol Program, Toronto, ON M5G 1X8, Canada
[2] NCI, Bethesda, MD 20892 USA
[3] Salk Inst, Gene Express Lab, San Diego, CA 92186 USA
[4] Univ Toronto, Dept Mol & Med Genet, Toronto, ON, Canada
基金:
加拿大健康研究院;
关键词:
D O I:
10.1093/nar/gki747
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The origin of DNA replication in the human beta-globin gene contains an initiation region (IR) and two flanking auxiliary elements. Two replicator modules are located within the upstream auxiliary sequence and the IR core, but the functional sequences in the downstream auxiliary element are unknown. Here, we use a combination of benzoylated-naphthoylated DEAE (BND) cellulose purification and nascent strand abundance assays to show that replication initiation occurs at the beta-globin 3' enhancer on human chromosome 11 in the Hu11 hybrid murine erythroleukemia (MEL) cell line. To examine replicator function, 3' enhancer fragments were inserted into an ectopic site in MEL cells via an optimized FRT/EGFP-FLP integration system. These experiments demonstrate that the 1.6 kb downstream auxiliary element is a third replicator module called bGRep-E in erythroid cells. The minimal 260 bp 3' enhancer is required but not sufficient to initiate efficient replication, suggesting cooperation with adjacent sequences. The minimal 3' enhancer also cooperates with elements in an expressing HS3 beta/gamma-globin construct to initiate replication. These data indicate that the beta-globin replicator has multiple initiation sites in three closely spaced replicator modules. We conclude that a mammalian enhancer can cooperate with adjacent sequences to create an efficient replicator module.
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页码:4412 / 4424
页数:13
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