Zhou Xiaoshan, Solaroli Nicola, Bjerke Mia, Stewart James B, Rozell Björn, Johansson Magnus, Karlsson Anna
Department of Laboratory Medicine, Karolinska Institute, S-141 86 Huddinge, Sweden.
Hum Mol Genet. 2008 Aug 1;17(15):2329-35. doi: 10.1093/hmg/ddn133. Epub 2008 Apr 22.
Deficient enzymatic activity of the mitochondrial deoxyribonucleoside kinases deoxyguanosine kinase (DGUOK) or thymidine kinase 2 (TK2) cause mitochondrial DNA (mtDNA)-depletion syndromes in humans. Here we report the generation of a Tk2-deficient mouse strain and show that the mice develop essentially normally for the first week but from then on exhibit growth retardation and die within 2-4 weeks of life. Several organs including skeletal muscle, heart, liver and spleen showed progressive loss of mtDNA without increased mtDNA mutations or structural alterations. There were no major histological changes in skeletal muscle, but heart muscle showed disorganized and damaged muscle fibers. Electron microscopy showed mitochondria with distorted cristae. The Tk2-deficient mice exhibited pronounced hypothermia and showed loss of hypodermal fat and abnormal brown adipose tissue. We conclude that Tk2 has a major role in supplying deoxyribonucleotides for mtDNA replication and that other pathways of deoxyribonucleotide synthesis cannot compensate for loss of this enzyme.
线粒体脱氧核糖核苷激酶脱氧鸟苷激酶(DGUOK)或胸苷激酶2(TK2)的酶活性缺陷会导致人类线粒体DNA(mtDNA)耗竭综合征。在此,我们报告了一种Tk2基因缺陷小鼠品系的产生,并表明这些小鼠在出生后的第一周基本正常发育,但从那时起开始出现生长迟缓,并在出生后2至4周内死亡。包括骨骼肌、心脏、肝脏和脾脏在内的多个器官显示出mtDNA逐渐丢失,而mtDNA突变或结构改变并未增加。骨骼肌没有明显的组织学变化,但心肌显示出肌纤维紊乱和受损。电子显微镜显示线粒体嵴扭曲。Tk2基因缺陷小鼠表现出明显的体温过低,皮下脂肪减少,棕色脂肪组织异常。我们得出结论,Tk2在为mtDNA复制提供脱氧核糖核苷酸方面起主要作用,并且脱氧核糖核苷酸合成的其他途径无法弥补该酶的缺失。