Aksoy S, Lalor T M, Martin J, Van der Ploeg L H, Richards F F
Yale MacArthur Center for Molecular Parasitology, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06510.
EMBO J. 1987 Dec 1;6(12):3819-26. doi: 10.1002/j.1460-2075.1987.tb02718.x.
The 140-nucleotide spliced leader (SL) RNA, involved in mRNA maturation in the African trypanosomes and in other kinetoplastida, is encoded by a tandem array of spliced leader genes. We show that the 1.4-kb SL gene repeat unit in Trypanosoma gambiense is organized in tandem arrays confined to two large (minimum size 350-450 kb) restriction fragments. SL genes in both arrays are interrupted by a total of eight conserved insertion elements. Cleavage of genomic DNA at restriction sites present within the insertion element but not in the SL gene repeat, releases variable numbers of SL genes from the tandem array. Since the insertion element contains a terminal poly(A) track of 36 bases and because a 49-bp duplication of target DNA has occurred at the integration site, we conclude that it is a retroposon. This retropson is uniquely associated with the SL gene clusters. These retroposons presumably originated from a single insertion event after which their copy number increased, possibly through unequal sister chromatid exchange.
140个核苷酸的剪接前导序列(SL)RNA参与非洲锥虫和其他动基体目生物的mRNA成熟过程,由剪接前导基因的串联阵列编码。我们发现,冈比亚锥虫中1.4kb的SL基因重复单元以串联阵列形式组织,局限于两个大的(最小尺寸为350 - 450kb)限制性片段。两个阵列中的SL基因总共被八个保守插入元件打断。在插入元件内而非SL基因重复序列中的限制性位点切割基因组DNA,会从串联阵列中释放出数量可变的SL基因。由于插入元件包含一个36个碱基的末端聚腺苷酸序列,并且在整合位点发生了49bp的靶DNA重复,我们得出结论,它是一个反转录转座子。这个反转录转座子与SL基因簇独特相关。这些反转录转座子可能起源于单个插入事件,之后其拷贝数增加,可能是通过不等姐妹染色单体交换实现的。