DISRUPTION OF THE ADENOSINE-DEAMINASE GENE CAUSES HEPATOCELLULAR IMPAIRMENT AND PERINATAL LETHALITY IN MICE

被引:128
作者
WAKAMIYA, M
BLACKBURN, MR
JURECIC, R
MCARTHUR, MJ
GESKE, RS
CARTWRIGHT, J
MITANI, K
VAISHNAV, S
BELMONT, JW
KELLEMS, RE
FINEGOLD, MJ
MONTGOMERY, CA
BRADLEY, A
CASKEY, CT
机构
[1] BAYLOR COLL MED, DEPT BIOCHEM, HOUSTON, TX 77030 USA
[2] BAYLOR COLL MED, CTR COMPARAT MED, HOUSTON, TX 77030 USA
[3] BAYLOR COLL MED, DEPT PATHOL, HOUSTON, TX 77030 USA
[4] BAYLOR COLL MED, HOWARD HUGHES MED INST, HOUSTON, TX 77030 USA
关键词
D O I
10.1073/pnas.92.9.3673
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have generated mice with a null mutation at the Ada locus, which encodes the purine catabolic enzyme adenosine deaminase (ADA, EC 3.5.4.4), ADA-deficient fetuses exhibited hepatocellular impairment and died perinatally, Their lymphoid tissues were not largely affected, Accumulation of ADA substrates was detectable in ADA-deficient conceptuses as early as 12.5 days postcoitum, dramatically increasing during late in utero development, and is the likely cause of liver damage and fetal death. The results presented here demonstrate that ADA is important for the homeostatic maintenance of purines in mice.
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收藏
页码:3673 / 3677
页数:5
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