Herrick G, Cartinhour S, Dawson D, Ang D, Sheets R, Lee A, Williams K
Cell. 1985 Dec;43(3 Pt 2):759-68. doi: 10.1016/0092-8674(85)90249-1.
A novel family of micronuclear elements termed telomere-bearing elements (TBEs) is described. All 1900 family members are eliminated during macronuclear development. We conclude that they are transposons, first because the members are moderately conserved in sequence and probably dispersed in the genome. Second, in two cases, sequence comparison of the termini and flanks of the element with the corresponding empty site indicate that elements cause 3 bp target duplications (AAT) upon insertion; the 3 bp are part of the 5 bp target sequence, AATGA. Lastly, both elements carry 77 or 78 bp inverted terminal repeats. The tip of each inverted terminal repeat is the 17 bp telomere-like sequence 5' C1A4C4A4C4. At least half of the elements have these 17 bp or an extremely similar sequence. One possible pathway for transposition into new micronuclear sites starts in the developing macronucleus with excision to create a free linear form to which telomeres are added, followed by a low frequency of movement to the micronucleus, and insertion into the germ-line micronuclear DNA.
本文描述了一类新的微核元件,称为端粒携带元件(TBEs)。在大核发育过程中,所有1900个家族成员都会被消除。我们得出结论,它们是转座子,首先是因为这些成员在序列上有适度的保守性,并且可能分散在基因组中。其次,在两个案例中,元件末端和侧翼与相应空位的序列比较表明,元件插入时会导致3 bp的靶标重复(AAT);这3 bp是5 bp靶标序列AATGA的一部分。最后,两个元件都带有77或78 bp的反向末端重复序列。每个反向末端重复序列的末端是17 bp的端粒样序列5' C1A4C4A4C4。至少一半的元件具有这17 bp或极其相似的序列。一种可能的转座到新微核位点的途径始于发育中的大核,通过切除产生一个游离的线性形式,在其上添加端粒,随后以低频率移动到微核,并插入种系微核DNA中。