Loss of E2F4 activity leads to abnormal development of multiple cellular lineages

被引:134
作者
Rempel, RE
Saenz-Robles, MT
Storms, R
Morham, S
Ishida, S
Engel, A
Jakoi, L
Melhem, MF
Pipas, JM
Smith, C
Nevins, JR [1 ]
机构
[1] Duke Univ, Med Ctr, Howard Hughes Med Inst, Dept Genet, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[3] Univ Pittsburgh, Sch Med, Dept Biol Sci, Pittsburgh, PA 15260 USA
[4] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA 15260 USA
[5] Myriad Genet, Salt Lake City, UT 84108 USA
关键词
D O I
10.1016/S1097-2765(00)00030-7
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 have generated mice deficient in E2F4 activity, the major form of E2F in many cell types. Analysis of newborn pups deficient in E2F4 revealed abnormalities in hematopoietic lineage development as well as defects in the development of the gut epithelium. Specifically, we observed a deficiency of various mature hematopoietic cell types together with an increased number of immature cells in several lineages. This was associated with an increased frequency of apoptotic cells. We also found a substantial reduction in the thickness of the gut epithelium that normally gives rise to crypts as well as a reduction in the density of villi. These observations suggest a critical role for E2F4 activity in controlling the maturation of cells in a number of tissues.
引用
收藏
页码:293 / 306
页数:14
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