Bozzoni I, Fragapane P, Annesi F, Pierandrei-Amaldi P, Amaldi F, Beccari E
J Mol Biol. 1984 Dec 25;180(4):987-1005. doi: 10.1016/0022-2836(84)90267-5.
The expression of two Xenopus laevis ribosomal protein genes (L1 and L14) has been analysed by microinjection of the cloned genomic sequences into frog oocyte nuclei. While the injection of the L14 gene causes the accumulation of the corresponding protein in large excess with respect to that synthesized endogenously, the L1 gene does not. Analysis of the RNA shows that both genes are actively transcribed. The seven-intron-containing L14 transcript is completely processed to a mature form, while two out of nine intron sequences persist in the L1 transcript. This precursor RNA is confined to the nucleus; its accumulation is due to a specific block of splicing operating at the level of two defined introns and not to saturation of the processing apparatus of the oocyte. The different behaviour of the two genes may reflect different mechanisms of regulation which, in the case of the L1 gene, could operate at the level of splicing.
通过将克隆的基因组序列显微注射到蛙卵母细胞核中,对非洲爪蟾的两个核糖体蛋白基因(L1和L14)的表达进行了分析。虽然注射L14基因会导致相应蛋白质的积累量大大超过内源性合成的量,但L1基因则不然。对RNA的分析表明,两个基因均被积极转录。含有7个内含子的L14转录本被完全加工成成熟形式,而L1转录本的9个内含子序列中有2个保留下来。这种前体RNA局限于细胞核内;其积累是由于在两个特定内含子水平上发生的剪接特异性阻断,而不是由于卵母细胞加工装置的饱和。这两个基因的不同行为可能反映了不同的调控机制,就L1基因而言,这种调控可能在剪接水平上发挥作用。