Szkukalek A, Mougin A, Grégoire A, Solymosy F, Branlant C
Laboratoire d' Enzymologie et de Génie Génétique, URA CNRS 457, Université Henri-Poincaré, Nancy I. Faculté des Sciences, Vandoeuvre-lès-Nancy, France.
Biochimie. 1996;78(6):425-35. doi: 10.1016/0300-9084(96)84749-3.
The 5' terminal sequence of U1 snRNA that base-pairs with the intron 5' splice site in the course of spliceosome assembly was considered to be universally conserved. A study of the P polycephalum U1 snRNA at both RNA and gene levels shows that there are exceptions to this rule: the P polycephalum U1 snRNA has a U to A substitution at position 5, that is partially compensated by a high frequency of T residue at position +4 of introns. In contrast to the yeast genome, the P polycephalum genome contains several U1 snRNA coding sequences (about 20). They either encode the U1A snRNA expressed in microplasmodia or correspond to the previously cloned U1B coding sequence. Both coding sequences show the U5A substitution. The ratio of U1A versus U1B coding sequences is of about 3. A U1A gene was cloned. The 60 nt region upstream of the coding sequence has the same sequence as in the U1B gene. The U1B gene is probably expressed at another stage of the P polycephalum life cycle.
在剪接体组装过程中与内含子5'剪接位点碱基配对的U1 snRNA的5'末端序列被认为是普遍保守的。对多头绒泡菌U1 snRNA在RNA和基因水平上的研究表明,这一规则存在例外情况:多头绒泡菌U1 snRNA在第5位有一个从U到A的替换,这在一定程度上被内含子第+4位高频率的T残基所补偿。与酵母基因组不同,多头绒泡菌基因组包含多个U1 snRNA编码序列(约20个)。它们要么编码在微原质团中表达的U1A snRNA,要么对应于先前克隆的U1B编码序列。这两个编码序列都显示出U5A替换。U1A与U1B编码序列的比例约为3。克隆了一个U1A基因。编码序列上游60 nt区域的序列与U1B基因中的相同。U1B基因可能在多头绒泡菌生命周期的另一个阶段表达。