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1 wo hexameric half-sites separated by 3 bp of spacer DNA.
2 ependent on conformational variations in the spacer DNA.
3 A show that the protein does not contact the spacer DNA.
4 as weaker than HS2 and more sensitive to the spacer DNA.
5 contact is seen between the proteins and the spacer DNA.
6 tes containing two CGG triplets separated by spacer DNA.
7 x to be the minimal machinery that catalyses spacer DNA acquisition and explain the significance of C
8 heterogeneity in telomere addition sites for spacer DNA also resembles the situation found for telome
9 that the most inactive promoters have short spacer DNA and the NtrC sites on the opposite side of th
10 t of CGG triplets, in contacting a TA in the spacer DNA, and in making direct dimer contacts between
11 ial (cox1) and nuclear (internal transcribed spacer) DNA data from the Schistosoma eggs or miracidia
16 mere addition, we sought to determine if the spacer DNAs might also undergo telomere addition prior t
17 ally interchangeable and require an internal spacer DNA of minimal length between 238 and 325 bp to b
20 s are typically separated from each other by spacer DNA segments, which are eliminated following chro
22 DNA elements differing in the length of the spacer DNA that separates two conserved recognition moti
24 with a specific geometry is required in the spacer DNA, to bring the Sin dimers at sites I and II to
27 pacer' DNA, but how they avoid targeting the spacer DNA within the encoding CRISPR locus itself is un
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