ライフサイエンスコーパス: sporophytic

1 raceae, SI in S. squalidus is expected to be sporophytic.

2 E (TIO) is essential for cytokinesis in both sporophytic and gametophytic cell types.

3 s species, lipids are major products of both sporophytic and gametophytic metabolism during pollen de

4 f the mutant alleles pointed to a dual role, sporophytic and gametophytic, for the gene on the male s

5 The plant life cycle includes diploid sporophytic and haploid gametophytic generations.

6 that the SI system of S. squalidus is indeed sporophytic and is controlled by a single multiallelic S

7 higher plants alternates between the diploid sporophytic and the haploid gametophytic phases.

8 ree known and ancient hormonal regulators of sporophytic branching interact to generate the branching

9 ication of premeiotic gamete precursors from sporophytic cells in the ovule.

10 can induce an egg cell-like transcriptome in sporophytic cells of A. thaliana.

11 To examine sphingolipid function in sporophytic cells, Arabidopsis lines were generated that

12 he haploid female gametophyte or the diploid sporophytic cells.

13 his indirectly through its influence on some sporophytic cells.

14 but all ovules contain genotypically normal sporophytic cells.

15 is MALE STERILITY1 gene, which is a critical sporophytic controlling factor for anther and pollen dev

16 her, this study reveals a chalazal-localized sporophytic cytokinin signal that plays an important rol

17 ype appeared to be caused by an unidentified sporophytic defect due to the mutation.

18 Homozygous myb98 mutants exhibit no sporophytic defects, including trichome and endosperm de

19 related and linked genes, GSL1 and GSL5, in sporophytic development and in reproduction.

20 t at least partially redundant roles in both sporophytic development and in the development of pollen

21 edundantly as an important control point for sporophytic development controlling male gametophyte pro

22 Sporophytic development was nearly normal in gsl1-1 homo

23 mRNA accumulation differ in scutella during sporophytic development.

24 buted by both the gametophytic (haploid) and sporophytic (diploid) genomes.

25 sterility of mpk3(+/-) mpk6(-/-) plants is a sporophytic effect.

26 a form of parental imprinting, and maternal sporophytic effects were detected.

27 idopsis genome not represented in studies of sporophytic expression and function.

28 The sporophytic expression of this gene is therefore also im

29 tified genes were not previously detected by sporophytic expression profiling, suggesting that the em

30 ies for immunoblotting after SDS-PAGE of the sporophytic extracts of B. napus developing anthers, two

31 map all five centromeres, easily distinguish sporophytic from gametophytic mutations, and accurately

32 productive cells develop in the plant body ("sporophytic generation") and then differentiate into a m

33 lele does not remain silenced throughout the sporophytic generation.

34 plant genome are derived primarily from the sporophytic generation.

35 is tightly regulated by maternal zygotic and sporophytic genes, some of which are subject to a parent

36 le paternity, spatial genetic structure, and sporophytic inbreeding depression in natural populations

37 In line with the prediction of sporophytic inbreeding depression sporophyte size was si

38 on, generating the female gametophyte within sporophytic integuments.

39 that is ancient and common to plants without sporophytic leaves.

40 pmental methylation reprogramming during the sporophytic life cycle of flowering plants regulates gen

41 synthetic and perception mutants is profound sporophytic male sterility characterized by failure of s

42 Mutations with both sporophytic maternal effects and gametophytic maternal e

43 were considered including triploid, diploid, sporophytic maternal, and maternal and paternal zygotic

44 at is, homomorphic gametophytic, homomorphic sporophytic or heteromorphic SI.

45 ing two to four nuclei, and random groups of sporophytic ovule cells not undergoing these events were

46 The sporophytic ovule cells were enriched in signaling funct

47 terning is a key divergence point from known sporophytic pathways.

48 dult plants have a reduced fitness in the 2N sporophytic portion of the life cycle, consistent with t

49 ophytic selection than on genes solely under sporophytic selection.

50 ata, a member of the Brassicaceae that has a sporophytic self-incompatibility (SI) system.

51 f S alleles, S. squalidus maintains a strong sporophytic self-incompatibility (SSI) system and there

52 logic considerations and the distribution of sporophytic self-incompatibility among these species dem

53 and the S-locus receptor kinase (SRK) of the sporophytic self-incompatibility system (SSI) in crucife

54 ation; within-morph crosses are impeded by a sporophytic self-incompatibility system.

55 r of species within the Brassicaceae express sporophytic self-incompatibility, under which individual

56 Twenty-six individuals of the sporophytic self-incompatible (SSI) weed, Senecio squali

57 Sporophytic selfing has much stronger effects: even a sm

58 by the same haploid individual, while under sporophytic selfing, a proportion of fertilizations invo

59 ly efflux carriers are primary regulators of sporophytic shoot development in flowering plants, the e

60 Sporophytic SI (SSI) is controlled by a single multi-all

61 ce/recessive relationships characteristic of sporophytic SI (SSI).

62 in higher plants are embedded in specialized sporophytic structures (ovules).

63 In sporophytic systems (SSI), the recognition phenotype of

64 hough the same genes may be expressed in the sporophytic tapetal cells and in gametophytic tissues, t

65 wall (exine) are contributed by surrounding sporophytic tapetal cells.

66 lly non-conserved C-terminal domain with the sporophytic tapetum oleosins.

67 grains are symplasmically isolated from the sporophytic tissue and rely on the nutrients and other c

68 oportion (70%) of the genes expressed in the sporophytic tissue but not in the pollen.

69 nized communication between gametophytic and sporophytic tissue is crucial for successful reproductio

70 fflux that directs patterning in the diploid sporophytic tissues comprising the rest of the plant.

71 In flowering plants, diploid sporophytic tissues in ovules and anthers support meiosi

72 xpressed in populations of dividing cells in sporophytic tissues of the plant body, such as the palis

73 hat MYB108 expression is largely confined to sporophytic tissues of the stamen.

74 se truncated versions of PDIL2-1 function in sporophytic tissues to affect ovule structure and impede

75 enes were expressed both in gametophytic and sporophytic tissues, although under different temporal r

76 usage of flavonoid glycosyltransferases from sporophytic tissues, F3GalTase uses only UDP-galactose a

77 Compared with sporophytic tissues, the young transcriptomes of the mal

78 ubset of genes, including those expressed in sporophytic tissues, was developmentally regulated durin

79 ressed in second generation C. thalictroides sporophytic tissues.

80 hown to be expressed in sperm cells and some sporophytic tissues.

81 ally or preferentially expressed relative to sporophytic tissues.

82 phyte, and six genes are highly expressed in sporophytic tissues.

83 to the intimate association of gametes with sporophytic tissues.

84 e haploid (gametophytic) as well as diploid (sporophytic) tissues of the developing ovule.

85 onditional male sterility in the mutant is a sporophytic trait, and when the double mutant was grown

86 e or whether it is primarily a subset of the sporophytic transcriptome.

87 ns of diploid Arabidopsis lyrata exhibit the sporophytic type of self-incompatibility system characte