TL;DR: It is proposed that the G-quartet structure must be dealt with in vivo by the telomere replication machinery, hydrogen-bonded structures formed from four guanosine residues in a square-planar array.
TL;DR: The complete nucleotide sequence of the small-subunit ribosomal RNA genes for the ciliate protozoans Stylonychia pustulata and Oxytricha nova are determined and are homologous and sufficiently similar that these organisms must be closely related.
Abstract: We have determined the complete nucleotide sequence of the small-subunit ribosomal RNA genes for the ciliate protozoans Stylonychia pustulata and Oxytricha nova. The sequences are homologous and sufficiently similar that these organisms must be closely related. In a phylogeny inferred from comparisons of several eukaryotic small-subunit ribosomal RNAs, the divergence of the ciliates from the eukaryotic line of descent is seen to coincide with the radiation of the plants, the animals, and the fungi. This radiation is preceded by the divergence of the slime mold, Dictyostelium discoideum.
TL;DR: The sequence d(GGGGTTTTGGGG) from the 3' overhang of the Oxytricha telomere has been crystallized and its three-dimensional structure solved to 2.5 Å resolution, showing that the structure has some intrinsic flexibility.
Abstract: The sequence d(GGGGTTTTGGGG) from the 3' overhang of the Oxytricha telomere has been crystallized and its three-dimensional structure solved to 2.5 A resolution. The oligonucleotide forms hairpins, two of which join to make a four-stranded helical structure with the loops containing four thymine residues at either end. The guanine residues are held together by cyclic hydrogen bonding and an ion is located in the centre. The four guanine residues in each segment have a glycosyl conformation that alternates between anti and syn. There are two four-stranded molecules in the asymmetric unit showing that the structure has some intrinsic flexibility.
TL;DR: 1H NMR spectroscopy is used to study the conformations of the DNA oligonucleotides d(G4T4G4) (Oxy-1.5), which contain the Oxytricha telomere repeat (T3G4), and d(T4T 4G4 T4G 4T4 G-quartet) (oxy-3.5) which are found to form a symmetrical bimolecular and an int
Abstract: THE telomeres of most eukaryotes contain a repeating G-rich sequence with the consensus d(T/A)1–4G1–8, of which 12–16 bases form a 3' single-strand overhang beyond the telomeric duplex1. It has been proposed that these G-rich oligonucleotides associate to form four-stranded structures from one2–4, two2,5 or four6,7 individual strands and that these structures may be relevant in vivo. The proposed structures contain Hoogsteen base-paired G-quartets, precedent for which has been in the literature for many years8. Here we use 1H NMR spectroscopy to study the conformations of the DNA oligonucleotides d(G4T4G4) (Oxy-1.5) and d(G4T4G4T4G4T4G4) (Oxy-3.5) which contain the Oxytricha telomere repeat (T4G4). We find that these molecules fold to form a symmetrical bimolecular and an intramolecular quadruplex, respectively. Both structures have four G-quartets formed from nucleotides that are alternately syn and anti along each strand. This arrangement differs from earlier models in which the strands are alternately all syn or all anti2,3,5. The T4 loops in Oxy-1.5 are on opposite ends of the quadruplex and loop diagonally across the G-quartet, resulting in adjacent strands being alternately parallel and antiparallel.
TL;DR: Two immunologically distinct proteins of 55 and 26 kd, which are tenaciously, but noncovalently associated with Oxytricha macronuclear DNA termini, have been purified and represent the first described example of telomeric-specific proteins.