ANALYSIS OF THE HUMAN CD10/NEUTRAL ENDOPEPTIDASE-24.11 PROMOTER REGION - 2 SEPARATE REGULATORY ELEMENTS

被引:39
作者
ISHIMARU, F
SHIPP, MA
机构
[1] DANA FARBER CANC INST,DEPT MED,DIV HEMATOL MALIGNANCIES,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,BOSTON,MA
关键词
D O I
10.1182/blood.V85.11.3199.bloodjournal85113199
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The cell surface zinc metalloproteinase CD10/neutral endopeptidase 24.11 (NEP) is expressed on normal and malignant lymphoid progenitors, granulocytes, and a variety of epithelial cells. To further define the tissue-specific and developmentally related expression of CD10/NEP, we have characterized two separate regulatory regions that control the transcription of 5' alternatively spliced CD10/NEP transcripts. These type 1 and 2 CD10/NEP regulatory regions are both characterized by the presence of multiple transcription initiation sites and the absence of classic TATA boxes and consensus initiator elements. The purine-rich type 1 regulatory region, which includes 5' UTR exon 1 sequence, is characterized by multiple putative PU.1 binding sites and consensus ets-binding motifs. In marked contrast, the GC-rich type 2 regulatory region contains multiple putative Sp1 binding sites, a potential consensus retinoblastoma control element (RCE), and an inverted CCAAT box. In the majority of tissues examined to date, type 2 CD10/NEP transcripts were more abundant; the abundance of type 1 transcripts was more variable, with the highest type 1 levels in fetal thymus and certain lymphoblastic leukemia cell lines. (C) 1995 by The American Society of Hematology.
引用
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页码:3199 / 3207
页数:9
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