Cloning of the murine transcriptional corepressor component SAP18 and differential expression of its mRNA in the hematopoietic hierarchy

被引:19
作者
Boehmelt, G
Antonio, L
Iscove, NN
机构
[1] Univ Toronto, Ontario Canc Inst, Toronto, ON M5G 2M9, Canada
[2] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2M9, Canada
[3] Amgen Inc, Amgen Ctr, Thousand Oaks, CA 91320 USA
关键词
single cell PCR; subtractive hybridization; B2; element; alternative polyadenylation;
D O I
10.1016/S0378-1119(97)00648-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A differentially expressed sequence tag (EMegR4) was isolated from a subtractive hybridization between a single bipotent erythroid/megakaryocytic precursor (E/Meg) and a single bipotent neutrophil/macrophage precursor (N/M). It was used to clone a novel murine cDNA referred to as mSAP18. The full-length mSAP18 cDNA contains 3415 nucleotides and codes for a protein of 153 amino acids. The open reading frame shows 98 % identity to a human protein, SAP18, recently identified in a complex with the transcriptional corepressor mSin3 and histone deacetylase. mSAP18 cDNA harbours four polyadenylation sites and a B2 small interspersed repetitive element (SINE) in its 3' untranslated region. We demonstrate that mSAP18 RNA is expressed with stage and lineage specificity in the hematopoietic hierarchy, and that alternative polyadenylation sites are used. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:267 / 275
页数:9
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