1980
DOI: 10.1007/bf01276962
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The nucellar projection and modified aleurone in the crease region of developing caryopses of barley (Hordeum vulgare L. var.distichum)

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Cited by 53 publications
(35 citation statements)
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“…In the case of the wheat grain, the expression of proteolytic enzymes was also localized in the nucellar projection cells (DomõÂ nguez and Cejudo 1998). These cells have the characteristic morphology of transfer cells and are part of the nucellar tissue (Cochrane and Duus 1980). Four stages of dierentiation are distinguished in the nucellar projection cells of the wheat grain, cells located near the pigment strand being the least dierentiated (Wang et al 1994a).…”
Section: Introductionmentioning
confidence: 95%
“…In the case of the wheat grain, the expression of proteolytic enzymes was also localized in the nucellar projection cells (DomõÂ nguez and Cejudo 1998). These cells have the characteristic morphology of transfer cells and are part of the nucellar tissue (Cochrane and Duus 1980). Four stages of dierentiation are distinguished in the nucellar projection cells of the wheat grain, cells located near the pigment strand being the least dierentiated (Wang et al 1994a).…”
Section: Introductionmentioning
confidence: 95%
“…Regionalization of the endosperm results in four cell types: transfer cells, aleurone cells, starchy endosperm cells, and cells of the embryo surrounding region. The transfer cells differentiate very early and are observed over the nucellar projection, bordering the endosperm cavity (Cochrane and Duffus 1980;Thompson et al 2001). They present extensive cell wall invaginations and increased plasma membrane surface, facilitating nutrient uptake by the endosperm.…”
Section: Introductionmentioning
confidence: 99%
“…Highly differentiated TCs have also been found at the symplastic discontinuities between individuals belonging to different generations (e.g., at the interface between gametophyte and sporophyte generations [Ligrone and Gambardella, 1988] and at the base of seeds [Kiesselbach, 1949;Cochrane and Duffus, 1980;Offler and Patrick, 1993;Talbot et al, 2001]) and symbiotic species (e.g., at mycorrhizal and rhizobium-root nodule interfaces [Gunning et al, 1974;Allaway et al, 1985]), and even at points of plant-parasite interaction (e.g., in nematode infections [Jones and Northcote, 1972]). This work makes use of the maize (Zea mays) basal endosperm TC layer as a model for investigating the regulatory pathways that govern TC differentiation.…”
Section: Introductionmentioning
confidence: 99%