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Cutting edge:: Ig heavy chain 3′ HS1-4 directs correct spatial position-independent expression of a linked transgene to B lineage cells
被引:0
|作者:
Chauveau, C
Jansson, EÅ
Müller, S
Cogné, M
Pettersson, S
[1
]
机构:
[1] Karolinska Inst, Ctr Genom Res, S-17177 Stockholm, Sweden
[2] Fac Med Limoges, Lab Immunol Genet, F-87025 Limoges, France
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D O I:
暂无
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
The Ig H chain locus is regulated by a set of cis-acting elements, Hypersensitive sites (HS) located 3' of the IgH, HS1-4, has been suggested to act as a locus control region (LCR) in cell lines, To assess the proposed role of HS1-4 acting as an LCR, we generated transgenic mice harboring a V-H promoter-beta-globin reporter gene linked to the Ig H chain HS1-4 3'-regulatory sequences. Transgene expression is strictly confined to B 12-lymphocytes, vith no detectable expression outside the B cell lineage in all transgenic founder lines. Furthermore, reporter gene activity is integration independent but not copy number dependent. Thus, additional sequences are required to,allow the HS1-4 regulatory region to act as a classical LCR in mice. Our data are discussed in the contest of tissue-specific gene expression in B lineage cells.
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页码:4637 / 4641
页数:5
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