ライフサイエンスコーパス: pentatricopeptide repeat

1 dence that the maize (Zea mays) nuclear gene Pentatricopeptide repeat 2263 (PPR2263) encoding a DYW d

2 ly, which includes tetratricopeptide repeat, pentatricopeptide repeat, and the recently identified oc

3 Here, we demonstrate that Leucine Rich Pentatricopeptide Repeat Containing (LRPPRC) controls CD

4 Leigh Syndrome protein LRPPRC (leucine-rich pentatricopeptide repeat containing).

5 One was the leucine-rich pentatricopeptide-repeat containing protein (LRPPRC), wh

6 Here, we show that a heterodimer of pentatricopeptide repeat-containing (PPR) proteins, term

7 rans-acting small interfering RNA gene (TAS)-pentatricopeptide repeat-containing gene (PPR)-small int

8 We report identification of KPAF4, a pentatricopeptide repeat-containing PABP which sequester

9 ve binder of Beclin-1, known as leucine-rich pentatricopeptide repeat-containing protein (LRPPRC), an

10 ructurome in wild-type (WT) and leucine-rich pentatricopeptide repeat-containing protein (LRPPRC)-def

11 d by the recent finding by Fleck et al. that pentatricopeptide repeat-containing protein 1 (PTCD1) ge

12 t rare protein altering variants in the gene pentatricopeptide repeat-containing protein 1 (PTCD1) sh

13 ty and was mapped to an exonic region of the pentatricopeptide repeat-containing protein At4g02750-li

14 LRPPRC (leucine-rich pentatricopeptide repeat-containing protein) has a key r

15 cine rich repeat proteins and genes encoding pentatricopeptide repeat-containing proteins.

16 Here, we identify an essential pentatricopeptide repeat-containing RNA binding protein,

17 he FOXM1 directly bound to and increased the pentatricopeptide repeat domain 1 (PTCD1) protein, a mit

18 ipts, mitochondrial RNA polymerase (POLRMT), pentatricopeptide repeat domain 3 protein (PTCD3), and a

19 This encodes the leucine-rich pentatricopeptide repeat domain protein (LRPPRC), which

20 Here, we found that Drosophila leucine-rich pentatricopeptide repeat domain-containing protein 1 (Dm

21 Sequence analysis identified Rf5 as a pentatricopeptide repeat-encoding gene.

22 nd gene-specific RNA-binding proteins of the pentatricopeptide repeat family and others that impede t

23 FACTOR1 (MTL1) protein, a new member of the Pentatricopeptide Repeat family, and show that it is ess

24 The petuniaRf gene is a member of the pentatricopeptide repeat gene family (PPR), an unusually

25 genome containing large numbers of candidate pentatricopeptide repeat genes (PPRs).

26 entirely composed of 14 repeats of the 35-aa pentatricopeptide repeat motif.

27 sess the respective importance of individual pentatricopeptide repeat motifs in PRORP2 for RNA bindin

28 eous RNase P (PRORP) possesses two domains - pentatricopeptide repeat (PPR) and metallonuclease (NYN)

29 typical metallonuclease domain tethered to a pentatricopeptide repeat (PPR) domain by a structural zi

30 The pentatricopeptide repeat (PPR) family represents one of

31 RNA editing factors of the pentatricopeptide repeat (PPR) family show a very high d

32 putative RNA binding proteins in plants, the pentatricopeptide repeat (PPR) family, no physiologicall

33 nucleus-encoded RNA-binding proteins of the pentatricopeptide repeat (PPR) family, which bind upstre

34 AS1/2, produces tasiRNAs regulating a set of pentatricopeptide repeat (PPR) genes and has been charac

35 The pentatricopeptide repeat (PPR) is a degenerate 35-amino

36 The pentatricopeptide repeat (PPR) is a degenerate 35-amino

37 The 3' modifications are modulated by pentatricopeptide repeat (PPR) Kinetoplast Polyadenylati

38 Members of the PLS subclass of the pentatricopeptide repeat (PPR) motif-containing family a

39 It belongs to a growing family of pentatricopeptide repeat (PPR) motif-containing proteins

40 Pentatricopeptide repeat (PPR) motifs are alpha-helical

41 The pentatricopeptide repeat (PPR) protein family is a large

42 LRPPRC belongs to the pentatricopeptide repeat (PPR) protein family, originall

43 the 'editosome' that contains members of the pentatricopeptide repeat (PPR) protein family, the RNA e

44 of editing are recognized by members of the pentatricopeptide repeat (PPR) protein family.

45 We show that the pentatricopeptide repeat (PPR) protein RNA PROCESSING FA

46 In this paper, we show that the E(+)-type pentatricopeptide repeat (PPR) protein SLO2, which lacks

47 this line is caused by lack of a chloroplast pentatricopeptide repeat (PPR) protein that we named SUP

48 We describe a pentatricopeptide repeat (PPR) protein, PPR10, whose bin

49 leotide deletion in At3g61360 that encodes a pentatricopeptide repeat (PPR) protein.

50 Pentatricopeptide repeat (PPR) proteins (PPRPs) are enco

51 Pentatricopeptide repeat (PPR) proteins are a large fami

52 The pentatricopeptide repeat (PPR) proteins are at the core

53 Pentatricopeptide repeat (PPR) proteins are helical repe

54 Pentatricopeptide repeat (PPR) proteins are helical repe

55 Pentatricopeptide repeat (PPR) proteins are members of o

56 Nuclear encoded pentatricopeptide repeat (PPR) proteins are required as

57 Pentatricopeptide repeat (PPR) proteins bind RNA via a m

58 Pentatricopeptide repeat (PPR) proteins comprise a large

59 Pentatricopeptide repeat (PPR) proteins constitute a lar

60 end maturation posits that sequence-specific pentatricopeptide repeat (PPR) proteins define termini b

61 netic screens demonstrated a requirement for pentatricopeptide repeat (PPR) proteins for RNA editing.

62 Nuclear encoded pentatricopeptide repeat (PPR) proteins include an RNA b

63 Most plant pentatricopeptide repeat (PPR) proteins localize to and

64 RNA-binding pentatricopeptide repeat (PPR) proteins specifically rec

65 s, including several hundred nuclear-encoded pentatricopeptide repeat (PPR) proteins that regulate pl

66 Pentatricopeptide repeat (PPR) proteins with C-terminal

67 NA, a set of SSU ribosomal proteins, several pentatricopeptide repeat (PPR) proteins, and proteins no

68 sites are presumably recognized by up to 200 pentatricopeptide repeat (PPR) proteins.

69 ich was an expanding clade of genes encoding pentatricopeptide repeat (PPR) proteins.

70 nt organelles relies on specific RNA-binding pentatricopeptide repeat (PPR) proteins.

71 king discernible motifs and approximately 20 pentatricopeptide repeat (PPR) RNA binding proteins.

72 Many proteins of unknown function, including pentatricopeptide repeat (PPR), tetratricopeptide repeat

73 vents in plant mitochondria and plastids are pentatricopeptide repeat (PPR)-containing proteins with

74 roteins that has significantly expanded, the pentatricopeptide repeat (PPR)-containing proteins.

75 ied two independent defective genes encoding pentatricopeptide repeat (PPR)-like proteins [CELL WALL

76 F10 protein is characterized by a stretch of pentatricopeptide repeats (PPR) and a C-terminal extensi

77 In mammals, the leucine-rich pentatricopeptide repeat protein (LRPPRC) and the stem-l

78 e, we demonstrated that under Cd treatments, Pentatricopeptide Repeat Protein 1 (PPR1), the target of

79 family protein, ABC transporter G family and pentatricopeptide repeat protein are the major markers f

80 red for ORRM1 to interact with site-specific pentatricopeptide repeat protein editing factors.

81 A member of the pentatricopeptide repeat protein family that carries a p

82 ere, we studied the functions of Arabidopsis PENTATRICOPEPTIDE REPEAT PROTEIN FOR GERMINATION ON NaCl

83 77 editing, like the essential site-specific pentatricopeptide repeat protein LOW PSII ACCUMULATION66

84 ome profiling to revisit the function of the pentatricopeptide repeat protein LPE1, reported to stimu

85 rbcL, downstream of the binding site of the pentatricopeptide repeat protein MATURATION OF RBCL 1 (M

86 f one of these translational activators, the pentatricopeptide repeat protein Pet111p, with its presu

87 1 mRNA-specific translational activator, the pentatricopeptide repeat protein Pet309.

88 y been identified as a chloroplast-localized pentatricopeptide repeat protein that integrates informa

89 The loss of GUN1 (a plastid-localized pentatricopeptide repeat protein) is able to restore nuc

90 d to investigate the role of a PLS-subfamily pentatricopeptide repeat protein, Mitochondrial Editing

91 EME1), an Arabidopsis (Arabidopsis thaliana) pentatricopeptide repeat protein-encoding gene belonging

92 ying a mutation in a gene encoding a P-class pentatricopeptide repeat protein.

93 gene, which encodes a mitochondria-localized PentatricoPeptide Repeat protein.

94 show here that GUN1, a chloroplast-localized pentatricopeptide-repeat protein, and ABI4, an Apetala 2

95 nd mitochondria of flowering plants requires pentatricopeptide repeat proteins (PPR proteins) for sit

96 affected in RNA editing have shown that many pentatricopeptide repeat proteins (PPRs) are required fo

97 ipts and target several transcripts encoding pentatricopeptide repeat proteins and proteins of unknow

98 Pentatricopeptide repeat proteins constitute a large fam

99 p4 transcripts to the function of the P-type pentatricopeptide repeat proteins RNA PROCESSING FACTORs

100 ith genes encoding chloroplast ribosomal and pentatricopeptide repeat proteins well represented among

101 Additionally, we identified 71 pentatricopeptide repeat proteins, 29 membrane carriers/

102 1 and RPF8), both restorer of fertility like pentatricopeptide repeat proteins, are required for proc

103 Here, we characterize two pentatricopeptide repeat proteins, ORGANELLE TRANSCRIPT

104 process, requiring numerous nuclear-encoded pentatricopeptide repeat proteins.

105 rtility genes) has identified genes encoding pentatricopeptide-repeat proteins as key regulators of p

106 hypotheses, we examined whether a synthetic pentatricopeptide repeat (sPPR) protein can substitute f