Collins J, Forbes E, Anderson P
Department of Genetics, University of Wisconsin, Madison 53706.
Genetics. 1989 Jan;121(1):47-55. doi: 10.1093/genetics/121.1.47.
We describe genetic and molecular properties of Tc3, a family of transposable elements in Caenorhabditis elegans. About 15 Tc3 elements are present in the genomes of several different wild-type varieties of C. elegans, but Tc3 transposition and excision are not detected in these strains. Tc3 transposition and excision occur at high frequencies, however, in strain TR679, a mutant identified because of its highly active Tc1 elements. In TR679, Tc3 is responsible for several spontaneous mutations affecting the unc-22 gene. Tc3-induced mutations are unstable, and revertants result from precise or nearly precise excision of Tc3. Although Tc3 is very active in TR679, it is not detectably active in several other mutator mutants, all of which exhibit high levels of Tc1 activity. Tc3 is 2.5 kilobases long, and except for sequences near its inverted repeat termini, it is unrelated to Tc1. The termini of Tc3 are inverted repeats of at least 70 base pairs; the terminal 8 nucleotides of Tc3 are identical to 8 of the terminal 9 nucleotides of Tc1.
我们描述了秀丽隐杆线虫中一个转座元件家族Tc3的遗传和分子特性。在几种不同野生型秀丽隐杆线虫的基因组中大约存在15个Tc3元件,但在这些品系中未检测到Tc3的转座和切除。然而,在TR679品系中,Tc3的转座和切除高频发生,TR679是一个因其高活性Tc1元件而被鉴定出的突变体。在TR679中,Tc3导致了几个影响unc - 22基因的自发突变。Tc3诱导的突变不稳定,回复突变体是由Tc3的精确或近乎精确切除产生的。尽管Tc3在TR679中非常活跃,但在其他几个诱变突变体中未检测到其活性,所有这些诱变突变体都表现出高水平的Tc1活性。Tc3长2.5千碱基,除了其反向重复末端附近的序列外,它与Tc1无关。Tc3的末端是至少70个碱基对的反向重复序列;Tc3末端的8个核苷酸与Tc1末端9个核苷酸中的8个相同。