SLR1 function is dispensable for both self-incompatible rejection and self-compatible pollination processes inBrassica

1996 ◽  
Vol 9 (4) ◽  
pp. 203-208 ◽  
Author(s):  
T. M. Franklin ◽  
J. Oldknow ◽  
M. Trick
Keyword(s):  
Compatible Pollination

scholarly journals Deciphering the Stigmatic Transcriptional Landscape of Compatible and Self-Incompatible Pollinations in Brassica napus Reveals a Rapid Stigma Senescence Response Following Compatible Pollination

2013 ◽  
Vol 6 (6) ◽  
pp. 1988-1991 ◽  
Author(s):  
Subramanian Sankaranarayanan ◽  
Muhammad Jamshed ◽  
Srijani Deb ◽  
Kate Chatfield-Reed ◽  
Eun-Joo Gina Kwon ◽  
...  
Keyword(s):  
Brassica Napus ◽  
Transcriptional Landscape ◽  
Compatible Pollination

Stigma factors regulating self-compatible pollination

2010 ◽  
Vol 5 (2) ◽  
pp. 156-163 ◽  
Author(s):  
Xin-Qi Gao ◽  
Dongzi Zhu ◽  
Xiansheng Zhang
Keyword(s):  
Compatible Pollination

scholarly journals The molecular signatures of compatible and incompatible pollination

2018 ◽  
Author(s):  
Chie Kodera ◽  
Jérémy Just ◽  
Martine Da Rocha ◽  
Antoine Larrieu ◽  
Lucie Riglet ◽  
...  
Keyword(s):  
Global Analysis ◽  
Pollen Grains ◽  
Mitogen Activated Protein Kinase ◽  
Molecular Signatures ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide ◽  
Incompatible Pollination ◽  
Mitogen Activated Protein ◽  
Dependent Cell ◽  
Compatible Pollination

AbstractFertilization in flowering plants depends on the early contact and recognition of pollen grains by the receptive papilla cells of the stigma. To identify the associated molecular pathways, we developed a transcriptomic analysis based on single nucleotide polymorphisms (SNPs) present in twoArabidopsis thalianaaccessions, one used as female and the other as male. We succeeded in distinguishing 80 % of transcripts according to their parental origins and drew up a catalog of genes whose expression is modified after pollen-stigma interaction. Global analysis of our data reveals that pattern-triggered immunity (PTI)-associated transcripts are upregulated after compatible pollination. From our analysis, we predicted the activation of the Mitogen-activated Protein Kinase 3 on the female side after compatible pollination, which we confirmed through expression and mutant analysis. Our work defines the molecular signatures of compatible and incompatible pollination, highlights the active status of incompatible stigmas, and unravels a new MPK3-dependent cell wall feature associated with stigma-pollen interaction.

Pollen-Wall Proteins: The Fate of Intine-Held Antigens on the Stigma in Compatible and Incompatible Pollinations of Phalaris Tuberosa L

1971 ◽  
Vol 9 (1) ◽  
pp. 239-251
Author(s):  
R. B. KNOX ◽  
J. HESLOP-HARRISON
Keyword(s):  
Hydrolytic Enzymes ◽  
Pollen Grains ◽  
Pollen Wall ◽  
Immunofluorescence Technique ◽  
Antigenic Material ◽  
Compatible Pollination

By the use of an immunofluorescence technique, the main source of the antigens released by the pollen grains of Phalaris tuberosa L. (Gramineae) on leaching has been shown to be the intine. The main concentration is in the thickened zone underlying the germination pore. The intine is also the site of various hydrolytic enzymes. The fate of the intine-held antigens has been followed in compatible and incompatible pollinations. They are lost on to the stigma within 5-10 min, whether or not the pollen grains germinate. Where germination does occur after a compatible pollination, the antigens remain spread on the surface of the stigma cells after the tubes have penetrated. There is no indication that antigenic material of the same type is released during the further growth of the tubes. The possible roles of the intine-held materials as recognition substances in inter- and intra-specific compatibility reactions are discussed.

scholarly journals A Pollen Coat–Inducible Autoinhibited Ca2+-ATPase Expressed in Stigmatic Papilla Cells Is Required for Compatible Pollination in the Brassicaceae

2014 ◽  
Vol 26 (2) ◽  
pp. 636-649 ◽  
Author(s):  
Megumi Iwano ◽  
Motoko Igarashi ◽  
Yoshiaki Tarutani ◽  
Pulla Kaothien-Nakayama ◽  
Hideki Nakayama ◽  
...  
Keyword(s):  
Stigmatic Papilla ◽  
Pollen Coat ◽  
Compatible Pollination

scholarly journals Shortened anther–stigma distance reduces compatible pollination in two distylousPrimulaspecies

2015 ◽  
Vol 9 (2) ◽  
pp. 224-232 ◽  
Author(s):  
Shu-Juan Liu ◽  
Ling-Yun Wu ◽  
Shuang-Quan Huang
Keyword(s):  
Compatible Pollination

scholarly journals Interorgan Signaling following Pollination in Carnations

1999 ◽  
Vol 124 (6) ◽  
pp. 598-604 ◽  
Author(s):  
Michelle L. Jones ◽  
William R. Woodson
Keyword(s):  
Carboxylic Acid ◽  
Ethylene Production ◽  
Dianthus Caryophyllus ◽  
Acc Synthase ◽  
Acc Content ◽  
Compatible Pollination

Following a compatible pollination in carnation (Dianthus caryophyllus L. `White Sim'), a signal that coordinates postpollination events is translocated from the style to the ovary and petals. In this paper the roles of ethylene and its direct precursor, 1-aminocyclopropane-1-carboxylic acid (ACC), in this signaling were investigated. Following pollination, ethylene and ACC increased sequentially in styles, ovaries, and petals. Ethylene and ACC were highest initially in the stigmatic region of the style but by 24 hours after pollination were highest in the base. Activity of ACC synthase correlated well with ethylene production in styles and petals. In ovaries, ACC synthase activity decreased after pollination despite elevated ethylene production. Lack of ACC synthase activity in pollinated ovaries, coupled with high ACC content, suggests that ACC is translocated within the gynoecium. Further, detection of propylene from petals following application to the ovary provided evidence for movement of ethylene within the flower. Experiments that removed styles and petals at various times after pollination suggest there is a transmissible pollination signal in carnations that has reached the ovary by 12 hours and the petals by 14 to 16 hours.

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