Kozak L P
Genetics. 1985 May;110(1):123-43. doi: 10.1093/genetics/110.1.123.
The cerebellum of BALB/cJ mice has approximately 2.5 times as much glycerol-3-phosphate dehydrogenase (GPDH) as that of C57BL/6J mice. This difference in enzyme levels, which positively correlates with similar differences in the levels of hybridizable GPDH mRNA, is controlled by at least two unlinked regulatory loci and the structural gene, Gdc-1, located on chromosome 15. These regulatory loci, which act predominantly during the second and third weeks of postnatal cerebellar development and differentiation, have been separated from each other in the CXB recombinant inbred strains of mice. One regulatory locus, Gdcr-1, although unlinked to the structural gene, has an allele in BALB/c mice that preferentially enhances expression of the BALB/c structural allele at Gdc-1. The other locus, Gdcr-2, which may or may not be single, enhances GPDH expression at Gdc-1 irrespective of the allele present, as is commonly observed for loci acting from a distance. Measurements of GPDH mRNA in the recombinant inbred mice suggest that these regulatory genes act by modulating mRNA levels. Accordingly, the regulation of GPDH expression in the cerebellum of mice depends on a complex interaction of unlinked regulatory elements with regulatory elements near the structural gene. Furthermore, since the Gdc-1 locus is expressed in virtually every tissue of the mouse except blood and since the observed genetic variation is restricted to the cerebellum, it is likely that other tissues will have their own distinctive genetic mechanisms for modulating Gdc-1 expression.
BALB/cJ小鼠小脑的甘油-3-磷酸脱氢酶(GPDH)含量约为C57BL/6J小鼠的2.5倍。这种酶水平的差异与可杂交的GPDH mRNA水平的类似差异呈正相关,它受至少两个不连锁的调控基因座以及位于15号染色体上的结构基因Gdc-1控制。这些调控基因座主要在出生后小脑发育和分化的第二和第三周起作用,在小鼠的CXB重组近交系中已彼此分离。一个调控基因座Gdcr-1虽然与结构基因不连锁,但在BALB/c小鼠中有一个等位基因,它优先增强Gdc-1处BALB/c结构等位基因的表达。另一个基因座Gdcr-2可能是单一的,也可能不是,它会增强Gdc-1处的GPDH表达,而不管存在何种等位基因,这是远距离起作用的基因座常见的情况。对重组近交小鼠中GPDH mRNA的测量表明,这些调控基因通过调节mRNA水平起作用。因此,小鼠小脑中GPDH表达的调控取决于不连锁的调控元件与结构基因附近调控元件的复杂相互作用。此外,由于Gdc-1基因座几乎在小鼠除血液外的每个组织中都有表达,并且观察到的遗传变异仅限于小脑,很可能其他组织有其自身独特的调节Gdc-1表达的遗传机制。