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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 ion in nonseed plant gametophytes, ancestral sporophytic and nonmeristematic functions in land plants
8 higher plants alternates between the diploid sporophytic and the haploid gametophytic phases.
9 ree known and ancient hormonal regulators of sporophytic branching interact to generate the branching
10     Thus, in contrast to the role of ASF1 in sporophytic cell cycle progression, our data indicate th
11 ication of premeiotic gamete precursors from sporophytic cells in the ovule.
12 can induce an egg cell-like transcriptome in sporophytic cells of A. thaliana.
13          To examine sphingolipid function in sporophytic cells, Arabidopsis lines were generated that
14 he haploid female gametophyte or the diploid sporophytic cells.
15 his indirectly through its influence on some sporophytic cells.
16  but all ovules contain genotypically normal sporophytic cells.
17 is MALE STERILITY1 gene, which is a critical sporophytic controlling factor for anther and pollen dev
18 her, this study reveals a chalazal-localized sporophytic cytokinin signal that plays an important rol
19 ype appeared to be caused by an unidentified sporophytic defect due to the mutation.
20          Homozygous myb98 mutants exhibit no sporophytic defects, including trichome and endosperm de
21  related and linked genes, GSL1 and GSL5, in sporophytic development and in reproduction.
22 t at least partially redundant roles in both sporophytic development and in the development of pollen
23 edundantly as an important control point for sporophytic development controlling male gametophyte pro
24                                              Sporophytic development was nearly normal in gsl1-1 homo
25  mRNA accumulation differ in scutella during sporophytic development.
26 buted by both the gametophytic (haploid) and sporophytic (diploid) genomes.
27 sterility of mpk3(+/-) mpk6(-/-) plants is a sporophytic effect.
28  a form of parental imprinting, and maternal sporophytic effects were detected.
29 idopsis genome not represented in studies of sporophytic expression and function.
30                                          The sporophytic expression of this gene is therefore also im
31 tified genes were not previously detected by sporophytic expression profiling, suggesting that the em
32 ies for immunoblotting after SDS-PAGE of the sporophytic extracts of B. napus developing anthers, two
33 map all five centromeres, easily distinguish sporophytic from gametophytic mutations, and accurately
34 productive cells develop in the plant body ("sporophytic generation") and then differentiate into a m
35 lele does not remain silenced throughout the sporophytic generation.
36  plant genome are derived primarily from the sporophytic generation.
37 is tightly regulated by maternal zygotic and sporophytic genes, some of which are subject to a parent
38 le paternity, spatial genetic structure, and sporophytic inbreeding depression in natural populations
39               In line with the prediction of sporophytic inbreeding depression sporophyte size was si
40 on, generating the female gametophyte within sporophytic integuments.
41 that is ancient and common to plants without sporophytic leaves.
42 pmental methylation reprogramming during the sporophytic life cycle of flowering plants regulates gen
43 synthetic and perception mutants is profound sporophytic male sterility characterized by failure of s
44                          Mutations with both sporophytic maternal effects and gametophytic maternal e
45 were considered including triploid, diploid, sporophytic maternal, and maternal and paternal zygotic
46 , NO species accumulated in the degenerating sporophytic nucellus, and auxin efflux into the developi
47 due to an abnormal development of either the sporophytic or gametophytic anther tissues.
48 at is, homomorphic gametophytic, homomorphic sporophytic or heteromorphic SI.
49 ing two to four nuclei, and random groups of sporophytic ovule cells not undergoing these events were
50                                          The sporophytic ovule cells were enriched in signaling funct
51 terning is a key divergence point from known sporophytic pathways.
52 dult plants have a reduced fitness in the 2N sporophytic portion of the life cycle, consistent with t
53 t lead to the development of male and female sporophytic reproductive structures and associated gamet
54 ophytic selection than on genes solely under sporophytic selection.
55 ata, a member of the Brassicaceae that has a sporophytic self-incompatibility (SI) system.
56 f S alleles, S. squalidus maintains a strong sporophytic self-incompatibility (SSI) system and there
57 logic considerations and the distribution of sporophytic self-incompatibility among these species dem
58 and the S-locus receptor kinase (SRK) of the sporophytic self-incompatibility system (SSI) in crucife
59 dominance hierarchy formed by alleles at the sporophytic self-incompatibility system of the Brassicac
60 erennial oilseed crop and is assumed to have sporophytic self-incompatibility system-the genetic basi
61 irm that S. integrifolium does indeed have a sporophytic self-incompatibility system.
62 ation; within-morph crosses are impeded by a sporophytic self-incompatibility system.
63 r of species within the Brassicaceae express sporophytic self-incompatibility, under which individual
64                Twenty-six individuals of the sporophytic self-incompatible (SSI) weed, Senecio squali
65                                              Sporophytic selfing has much stronger effects: even a sm
66  by the same haploid individual, while under sporophytic selfing, a proportion of fertilizations invo
67 ly efflux carriers are primary regulators of sporophytic shoot development in flowering plants, the e
68                                              Sporophytic SI (SSI) is controlled by a single multi-all
69 ce/recessive relationships characteristic of sporophytic SI (SSI).
70 he significance and possible function of the sporophytic stomata are not well understood, hindering u
71 in higher plants are embedded in specialized sporophytic structures (ovules).
72 lopment in angiosperms occurs within diploid sporophytic structures and requires coordinated developm
73                                           In sporophytic systems (SSI), the recognition phenotype of
74 hough the same genes may be expressed in the sporophytic tapetal cells and in gametophytic tissues, t
75  wall (exine) are contributed by surrounding sporophytic tapetal cells.
76 lly non-conserved C-terminal domain with the sporophytic tapetum oleosins.
77 genotyping revealed that laboratory-cultured sporophytic thalli produced not only each type of gameto
78  thalli originally evolved via apomeiosis in sporophytic thalli.
79  grains are symplasmically isolated from the sporophytic tissue and rely on the nutrients and other c
80 oportion (70%) of the genes expressed in the sporophytic tissue but not in the pollen.
81 nized communication between gametophytic and sporophytic tissue is crucial for successful reproductio
82 ed set, we find that ACC signaling in ovular sporophytic tissue is involved in pollen tube attraction
83                               Tapetum, a key sporophytic tissue, provides nutrients for pollen develo
84 ametophyte pollen depends on the surrounding sporophytic tissue, the tapetum.
85  GSNOR protein is exclusively accumulated in sporophytic tissues and indirectly controls FG developme
86 fflux that directs patterning in the diploid sporophytic tissues comprising the rest of the plant.
87                 In flowering plants, diploid sporophytic tissues in ovules and anthers support meiosi
88 ernal bias, and siren expression in maternal sporophytic tissues is required for siren siRNA accumula
89 xpressed in populations of dividing cells in sporophytic tissues of the plant body, such as the palis
90 hat MYB108 expression is largely confined to sporophytic tissues of the stamen.
91 se truncated versions of PDIL2-1 function in sporophytic tissues to affect ovule structure and impede
92 enes were expressed both in gametophytic and sporophytic tissues, although under different temporal r
93 usage of flavonoid glycosyltransferases from sporophytic tissues, F3GalTase uses only UDP-galactose a
94                                Compared with sporophytic tissues, the young transcriptomes of the mal
95 ubset of genes, including those expressed in sporophytic tissues, was developmentally regulated durin
96 ressed in second generation C. thalictroides sporophytic tissues.
97 hown to be expressed in sperm cells and some sporophytic tissues.
98 ally or preferentially expressed relative to sporophytic tissues.
99 phyte, and six genes are highly expressed in sporophytic tissues.
100  to the intimate association of gametes with sporophytic tissues.
101 e haploid (gametophytic) as well as diploid (sporophytic) tissues of the developing ovule.
102 onditional male sterility in the mutant is a sporophytic trait, and when the double mutant was grown
103 e or whether it is primarily a subset of the sporophytic transcriptome.
104 ns of diploid Arabidopsis lyrata exhibit the sporophytic type of self-incompatibility system characte

 
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