Isolation and characterization of a novel epithelium-specific transcription factor, ESE-1, a member of the ets family

被引:203
作者
Oettgen, P
Alani, RM
Barcinski, MA
Brown, L
Akbarali, Y
Boltax, J
Kunsch, C
Munger, K
Libermann, TA
机构
[1] HARVARD UNIV, SCH MED, DEPT PATHOL, BOSTON, MA 02215 USA
[2] BETH ISRAEL DEACONESS MED CTR, DIV PATHOL, BOSTON, MA 02215 USA
[3] UNIV SAO PAULO, DEPT PARASITOL, BR-05508900 SAO PAULO, BRAZIL
[4] HUMAN GENOME SCI INC, ROCKVILLE, MD 20850 USA
关键词
D O I
10.1128/MCB.17.8.4419
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
We report here the isolation of a novel, highly tissue-restricted member of the ets transcription factor/oncogene family, ESE-1 (for epithelium-specific Ets), which has features distinct from those of any other eis-related factor, ESE-1 contains two putative DNA binding domains: an ETS domain, which is unique in that the 5' half shows relatively weak homology to known ets factors, and an A/T hook domain, found in HMG proteins and various other nuclear factors, In contrast to any known ets factors, ESE-1 is expressed exclusively in epithelial cells, ESE-1 expression is induced during terminal differentiation of the epidermis and in a primary human keratinocyte differentiation system. The keratinocyte terminal differentiation marker gene, SPRR2A, is a putative target for ESE-1, since SPRR2A expression during keratinocyte differentiation correlates with induction of ESE-1 expression, and ESE-1 binds with high affinity to and transactivates the ets binding site in the SPRR2A promoter, ESE-1 also binds to and transactivates the enhancer of the Endo A gene, a potential target for ESE-1 in simple epithelia. Due to the important role that other ets factors play in cellular differentiation, ESE-1 is expected to be a critical regulator of epithelial cell differentiation.
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页码:4419 / 4433
页数:15
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