ライフサイエンスコーパス: testa

1 dling roots, developing spikes, and pericarp/testa.

2 ng to the genotype of the maternally derived testa.

3 g a lineage dependence in development of the testa.

4 haliana MYB transcription factor TRANSPARENT TESTA 2 (TT2) in Medicago trunculata hairy roots induces

5 Expression of the Arabidopsis TRANSPARENT TESTA 2 (TT2) MYB family transcription factor leads to m

6 e and chalcone isomerase mutant (transparent testa 5, tt5) seedlings grown under anthocyanin inductiv

7 lated dark pigment in the cell layers of the testa above the endothelium, which itself accumulated pr

8 proteins include a family of proteins named TESTA ABUNDANT1 (TBA1) to TBA3; a less abundant fourth h

9 The toughening of the bks testa and associated poor germination were partially ove

10 By focusing on the stages between testa and endosperm rupture, we were able to circumvent

11 ot proximity to maternal tissues such as the testa and pericarp are important for aleurone developmen

12 er antioxidant activity than those with pale testa, and a positive correlation was found between tota

13 similar, with a round shape, a disorganized testa, and viviparism.

14 perm rupture, we were able to circumvent the testa barrier to the GUS substrate and observe diverse t

15 Bio- and physicochemical analysis of the bks testa determined that it accumulated a melanic substance

16 Whole seeds, seeds lacking the testa, embryos, and isolated aleurone layers of Arabidop

17 h revealed that different seed compartments (testa, endosperm, and embryo) control germination, but l

18 g seedling epidermal patterning, TRANSPARENT TESTA GLABRA (TTG) and WEREWOLF (WER), also control the

19 RHF induced by auxin in rhd6 and transparent testa glabra (ttg) mutants.

20 kers lutescens (lu; 17.6 cM) and transparent testa glabra (ttg; 35.5 cM) on the top arm of Arabidopsi

21 Five loci (TRANSPARENT TESTA GLABRA [TTG], GLABRA2 [GL2], ROOT HAIR DEFECTIVE6

22 (Petunia hybrida [petunia]) and TRANSPARENT TESTA GLABRA1 (TTG1) (Arabidopsis thaliana).

23 om petunia (Petunia hybrida) and TRANSPARENT TESTA GLABRA1 (TTG1) from Arabidopsis thaliana and assoc

24 The TRANSPARENT TESTA GLABRA1 (TTG1) locus regulates several development

25 Mutations in TRANSPARENT TESTA GLABRA1 (TTG1) result in several pleiotropic defec

26 tors, and a WD40 repeat protein, TRANSPARENT TESTA GLABRA1 (TTG1), act in concert to activate trichom

27 f the trichome promoting factors TRANSPARENT TESTA GLABRA1 (TTG1), GLABRA3 (GL3)/ENHANCER OF GL3 (EGL

28 (GL1; R2R3MYB), GL3 (bHLH), and transparent TESTA GLABRA1 (TTG1; WD40).

29 of trichome development, GL3 and TRANSPARENT TESTA GLABRA1, also impaired cuticle development and SAR

30 ranscriptional regulators MYB12, Transparent Testa Glabra1, and Production of Anthocyanin Pigment aft

31 the promoters of GLABRA2 (GL2), TRANSPARENT TESTA GLABRA2 (TTG2), CAPRICE (CPC) and ENHANCER OF TRIP

32 eles for endosperm growth factor transparent testa glabra2 and HAIKU1 and defense response regulators

33 t epidermal transcriptome of the transparent testa glabra2 mutant to clarify its role in the network.

34 of both the GLABROUS1 (GL1) and TRANSPARENT TESTA GLABROUS (TTG) genes.

35 abidopsis (Arabidopsis thaliana) transparent testa glabrous1 mutant.

36 successively after G lignin within the same testa layers, concurrently with apparent loss of the fun

37 C analyses revealed that several transparent testa lines blocked at intermediate steps of the flavono

38 This suggests that the testa manufactures components before its demise that can

39 yo produces factors that are conveyed to the testa, mitigating this process.

40 ion pattern was also examined in transparent testa mutants blocked at different steps in the flavonoi

41 ny of the 13 flavonoid-deficient transparent testa mutants for which a map position is known.

42 The transparent testa mutants were shown to have precursor accumulation

43 tannins (proanthocyanidins) in the pigmented testa of some sorghum cultivars have been implicated in

44 Samples with dark testa (or seed coat), namely black lentils and diavoli b

45 tment of seeds with PME resulted in enhanced testa permeability and promoted TR.

46 nsparent testa15 and displayed a transparent testa phenotype and a reduction in seed size.

47 hi mutant restores the seed coat transparent testa phenotype and the accumulation of flavonoids.

48 osynthesis is TT2, named for the transparent testa phenotype of tt2 mutant seeds that lack PAs in the

49 Mttt8 mutant seeds have a transparent testa phenotype with reduced PAs and anthocyanins.

50 atterns indicated a role for PME activity in testa rupture (TR).

51 a), PME activities peaked around the time of testa rupture but declined just before the completion of

52 mination, which was not connected to altered testa rupture morphology but to alterations of the micro

53 The ungerminated knockout seeds exhibited testa rupture, but failed to penetrate the endosperm lay

54 This increases again at testa rupture, the start of the second transcriptional p

55 ses during germination that are separated by testa rupture.

56 The Arabidopsis aberrant testa shape (ats) mutant produces a single integument in

57 that involves transcription factor ABERRANT TESTA SHAPE (ATS).

58 g ovule development, independent of ABERRANT TESTA SHAPE (ATS, also known as KANADI4) activity.

59 ABERRANT TESTA SHAPE (ATS, or KAN4) is necessary during ovule dev

60 ing the KANADI transcription factor ABERRANT TESTA SHAPE.

61 mponents before its demise that can maximize testa strength, whereas the endosperm/embryo produces fa

62 is probably due to the impermeability of the testa to the GUS substrate.

63 Mutations in the transparent testa (tt) loci abolish pigment production in Arabidopsi

64 HA10 result in seed coats with a transparent testa (tt) phenotype (light-colored seeds).

65 by comparing wild-type (WT) and transparent testa (tt4) plants with a mutation in the gene encoding