ライフサイエンスコーパス: Euplotes

1 GGGGTTTTGG) sequence found at DNA termini in Euplotes.

2 ar telomeres from the ciliates Oxytricha and Euplotes.

3 ptase (RT)-like proteins associated with the Euplotes aediculatus (Ea_p123), Saccharomyces cerevisiae

4 eated sequence, (TTTTGGGG)(n) in the ciliate Euplotes aediculatus and (TTAGGG)(n) in humans.

5 tein subunits of telomerase from the ciliate Euplotes aediculatus and the yeast Saccharomyces cerevis

6 e report the purification of telomerase from Euplotes aediculatus by affinity chromatography with ant

7 tein components, telomerase from the ciliate Euplotes aediculatus contains the subunit p43.

8 inks with the anchor site of telomerase from Euplotes aediculatus nuclear extract.

9 The stabilities of Euplotes aediculatus primer-telomerase complexes were de

10 e processivity of telomeric DNA extension by Euplotes aediculatus telomerase at various concentration

11 elomerase ribonucleoprotein from the ciliate Euplotes aediculatus to telomeric DNA in vitro has been

12 Telomerase was purified from Euplotes aediculatus, a ciliated protozoan, and one of i

13 In the ciliate Euplotes aediculatus, the protein p43 biochemically co-p

14 the same DNA-binding characteristics as the Euplotes and Oxytricha telomere-binding proteins.

15 ndently derived the same eRF1 specificity as Euplotes, and three spirotrichs, Stylonychia lemnae, S.

16 First, it is hosted by a ciliated protist, Euplotes; bacterial symbionts of ciliates are still poor

17 eotide was less precise than Tetrahymena and Euplotes but still had a bias that changed as a function

18 ies of the telomere end binding protein from Euplotes crassus (EcTEBP).

19 The transposon-like Tec elements of Euplotes crassus are precisely excised during formation

20 Telomerase from the ciliate Euplotes crassus incorporates G4T4telomeric repeats onto

21 e histone H3 genes of the ciliated protozoan Euplotes crassus indicates that one gene functions only

22 During sexual reproduction, Euplotes crassus precisely fragments its micronuclear ch

23 avage-elongation reaction carried out by the Euplotes crassus telomerase.

24 , rTP, is a nuclear protein from the ciliate Euplotes crassus that appears to be a novel telomere rep

25 Two genes have been cloned from the ciliate Euplotes crassus that encode proteins with sequence simi

26 R of TR3 with the corresponding segment of a Euplotes crassus TR restricted Sec insertion into the C-

27 istone H2B genes from the ciliated protozoan Euplotes crassus were cloned and sequenced.

28 In the ciliate Euplotes crassus, however, telomerase RNP structure and

29 rmation of a new macronucleus in the ciliate Euplotes crassus, micronuclear chromosomes are reproduci

30 In the ciliate Euplotes crassus, millions of new telomeres are synthesi

31 In Euplotes crassus, most of the micronuclear genome is eli

32 rminal domain of the OnTEBP alpha subunit in Euplotes crassus, Schizosaccharomyces pombe, and Homo sa

33 in Oxytricha trifallax, Stylonychia mytilis, Euplotes crassus, Schizosaccharomyces pombe, and Homo sa

34 In Euplotes crassus, telomerase is responsible for telomere

35 f selenocysteine and cysteine in the ciliate Euplotes crassus, that the dual use of this codon can oc

36 In the ciliate Euplotes crassus, the core telomerase ribonucleoprotein

37 ring macronuclear development in the ciliate Euplotes crassus, the highly repetitive, transposon-like

38 Similarities of the Euplotes fragmentation/telomere addition process to the

39 anslational frameshifting in ciliates of the Euplotes genus.

40 In contrast, the Euplotes hybrid facilitated efficient translation termin

41 Thus, telomerase expression in Euplotes is controlled by unique regulatory mechanisms t

42 These findings suggest that p43 is not the Euplotes La protein but instead plays a dedicated role i

43 th telomerase from vegetative and developing Euplotes macronuclei using chimeric primers that contain

44 lizes to the sites of DNA replication within Euplotes macronuclei.

45 ene, and that the structural arrangements of Euplotes mRNA preserve location-dependent dual function

46 one En-6 isolated from the antarctic species Euplotes nobilii.

47 demonstrated that a hybrid eRF1 carrying the Euplotes octocarinatus domain 1 fused to Saccharomyces c

48 ain 1 from either Tetrahymena thermophila or Euplotes octocarinatus fused to eRF1 domains 2 and 3 fro

49 of 'model' ciliates-Paramecium, Tetrahymena, Euplotes, Oxytricha and Stylonychia-reveal considerable

50 populations in the presence of the predator Euplotes patella.

51 The protozoan Euplotes pheromones were selected by fold recognition as

52 Euplotes provides a unique opportunity to study C strand

53 e Er-11 pheromone of the unicellular ciliate Euplotes raikovi, suggesting a possible common pathway f

54 Ciliates of Euplotes species constitutively secrete pleiotropic prot

55 es recognize only UGA as a stop codon, while Euplotes species recognize only UAA and UAG as stop codo

56 We show that purified Euplotes telomerase has no activity with blunt-ended pri

57 In this study we recruited the Euplotes telomerase to nontelomeric 3' termini in vitro

58 protein particles cooperate to elongate each Euplotes telomere in vivo.

59 mers are aligned with the G-rich strand of a Euplotes telomere, the cross-linked nucleotides correspo

60 at rTP binds specifically to the G-strand of Euplotes telomeric DNA and hence has some of the same DN

61 raints based on sequence alignments with the Euplotes templates and the attractin disulfide bonds.

62 We have used the ciliate Euplotes to study the role of DNA polymerase in telomeri

63 of the chromosome end-replicating enzyme in Euplotes, yeasts, and mammals.