Barzotti Rita, Pelliccia Franca, Rocchi Angela
Dipartimento di Genetica e Biologia Molecolare, Università La Sapienza, 00185 Roma, Italia.
Chromosome Res. 2003;11(4):365-73. doi: 10.1023/a:1024048108918.
Four different units containing three variants of the U1 snRNA gene have been identified in the genome of Asellus aquaticus and only one unit has been identified in the genome of Proasellus coxalis. All four identified U1 snRNA genes can be folded according to the proper secondary structure and possess the functionally useful conserved sequences. Moreover, in the 3 flanking regions, all genes present both the 3 box, a conserved sequence required for 3 processing of mature snRNA, and a polyadenylation signal which is unusual for these genes. The PCR products were used as probes in fluorescent in-situ hybridization (FISH) experiments to locate them on chromosomes of A. aquaticus and P. coxalis.
在普通等足虫的基因组中已鉴定出包含U1小核仁核糖核酸(snRNA)基因三种变体的四个不同单元,而在柯氏原等足虫的基因组中仅鉴定出一个单元。所有四个已鉴定的U1 snRNA基因都可以根据适当的二级结构进行折叠,并拥有功能上有用的保守序列。此外,在3'侧翼区域,所有基因都同时具有3'框(成熟snRNA的3'加工所需的保守序列)和多聚腺苷酸化信号,这对这些基因来说是不寻常的。聚合酶链反应(PCR)产物在荧光原位杂交(FISH)实验中用作探针,以将它们定位在普通等足虫和柯氏原等足虫的染色体上。