Collins J J, Anderson P
Department of Biochemistry and Molecular Biology, University of New Hampshire, Durham 03824.
Genetics. 1994 Jul;137(3):771-81. doi: 10.1093/genetics/137.3.771.
We have identified Tc5, a new family of transposable genetic elements in the nematode Caenorhabditis elegans. All wild-type varieties of C. elegans that we examined contain 4-6 copies of Tc5 per haploid genome, but we did not observe transposition or excision of Tc5 in these strains. Tc5 is active, however, in the mut-2 mutant strain TR679. Of 60 spontaneous unc-22 mutations isolated from strain TR679, three were caused by insertion of Tc5. All three Tc5-induced mutations are unstable; revertants results from precise or nearly precise excision of Tc5. Individual Tc5 elements are similar to each other in size and structure. The 3.2-kb element is bounded by inverted terminal repeats of nearly 500 bp. Eight of the ten terminal nucleotides of Tc5 are identical to the corresponding nucleotides of Tc4. Further, both elements recognize the same target site for insertion (CTNAG) and both cause duplication of the central TNA trinucleotide upon insertion. Other than these similarities to Tc4, Tc5 is unrelated to the three other transposon families (Tc1, Tc3 and Tc4) that transpose and excise at high frequency in mut-2 mutant strains. Mechanisms are discussed by which four apparently unrelated transposon families are all affected by the same mut-2 mutation.
我们在秀丽隐杆线虫中鉴定出了Tc5,这是一种新的可移动遗传元件家族。我们检测的所有秀丽隐杆线虫野生型品种,每个单倍体基因组中都含有4 - 6个Tc5拷贝,但在这些品系中我们未观察到Tc5的转座或切除现象。然而,Tc5在mut - 2突变体品系TR679中是活跃的。从品系TR679中分离出的60个自发unc - 22突变中,有三个是由Tc5插入引起的。所有这三个由Tc5诱导的突变都是不稳定的;回复突变是由Tc5的精确或近乎精确切除导致的。单个Tc5元件在大小和结构上彼此相似。这个3.2 kb的元件由近500 bp的反向末端重复序列界定。Tc5的十个末端核苷酸中有八个与Tc4的相应核苷酸相同。此外,这两个元件识别相同的插入靶位点(CTNAG),并且在插入时都会导致中央TNA三核苷酸的重复。除了与Tc4的这些相似之处外,Tc5与在mut - 2突变体品系中高频转座和切除的其他三个转座子家族(Tc1、Tc3和Tc4)无关。文中讨论了四个明显不相关的转座子家族都受相同mut - 2突变影响的机制。