synergid cell
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2021 ◽  
Author(s):  
Jennifer A. Noble ◽  
Alex Seddon ◽  
Sahra Uygun ◽  
Steven E. Smith ◽  
Shin-Han Shiu ◽  
...  

Synergid cells in the micropylar end of the female gametophyte are required for critical cell-cell signaling interactions between the pollen tube and the ovule that precede double fertilization and seed formation in flowering plants. LORELEI (LRE) encodes a GPI-anchored protein that is expressed primarily in the synergid cells, and together with FERONIA, a receptor-like kinase, it controls pollen tube reception by the receptive synergid cell. Still, how LRE expression is controlled in synergid cells remains poorly characterized. We identified candidate cis-regulatory elements enriched in LRE and other synergid cell-expressed genes. One of the candidate motifs (TAATATCT) in the LRE promoter was an uncharacterized variant of the Evening Element motif that we named as the Short Evening Element-like (SEEL) motif. Deletion or point mutations in the SEEL motif of the LRE promoter resulted in decreased reporter expression in synergid cells, demonstrating that the SEEL motif is important for expression of LRE in synergid cells. Additionally, we found that LRE expression is decreased in the loss of function mutants of REVEILLE (RVE) transcription factors, which are clock genes known to bind the SEEL and other closely related motifs. We propose that RVE transcription factors regulate LRE expression in synergid cells by binding to the SEEL motif in the LRE promoter. Identification of a cis-regulatory element and transcription factors involved in the expression of LRE will serve as a foundation to characterize the gene regulatory networks in synergid cells and investigate the potential connection between circadian rhythm and fertilization.



2019 ◽  
Author(s):  
Jing Yuan ◽  
Yan Ju ◽  
Daniel S. Jones ◽  
Weiwei Zhang ◽  
Noel Lucca ◽  
...  

AbstractDuring gamete delivery in Arabidopsis thaliana, intercellular communication between the attracted pollen tube and the receptive synergid cell leads to subcellular events in both cells culminating in the rupture of the tip-growing pollen tube and release of the sperm cells to achieve double fertilization. Live imaging of pollen tube reception revealed dynamic subcellular changes that occur in the female synergid cells. Pollen tube arrival triggers the trafficking of NORTIA (NTA) MLO protein from Golgi-associated compartments and the accumulation of endosomes at or near the synergid filiform apparatus, a membrane-rich region that acts as the site of communication between the pollen tube and synergids. Domain swaps and site-directed mutagenesis reveal that NTA’s C-terminal cytoplasmic tail with its calmodulin-binding domain influences the subcellular localization and function of NTA in pollen tube reception and that accumulation of NTA at the filiform apparatus is necessary and sufficient for MLO function in pollen tube reception.



2018 ◽  
Author(s):  
Sergio Galindo-Trigo ◽  
Noel Blanco-Touriñán ◽  
Thomas A. DeFalco ◽  
Eloise S. Wells ◽  
Julie E Gray ◽  
...  

AbstractCommunication between the gametophytes is vital for angiosperm fertilisation. Multiple CrRLK1L-type receptor kinases prevent premature pollen tube burst, while another CrRLK1L protein, FERONIA (FER), is required for pollen tube burst in the female gametophyte. We report here the identification of two additional CrRLK1L homologues, HERCULES RECEPTOR KINASE 1 (HERK1) and ANJEA (ANJ), which act redundantly to promote pollen tube burst at the synergid cells. HERK1 and ANJ localise to the filiform apparatus of the synergid cells in unfertilised ovules, and in herk1 anj mutants a majority of ovules remain unfertilised due to pollen tube overgrowth, together indicating that HERK1 and ANJ act as female determinants for fertilisation. As in fer mutants, the synergid cell-specific, endomembrane protein NORTIA (NTA) is not relocalised after pollen tube reception; however, unlike fer mutants, reactive oxygen species levels are unaffected in herk1 anj double mutants. Both ANJ and HERK1 associate with FER and its proposed co-receptor LORELEI (LRE) in planta. Together, our data indicate that HERK1 and ANJ act with FER to mediate female-male gametophyte interactions during plant fertilisation.



2018 ◽  
Vol 96 (1) ◽  
pp. 176-187 ◽  
Author(s):  
Cheng Zhang ◽  
Xiao-Dong Teng ◽  
Quan-Quan Zheng ◽  
Yan-Yun Zhao ◽  
Jie-Yang Lu ◽  
...  


2016 ◽  
Vol 34 ◽  
pp. 122-126 ◽  
Author(s):  
Daisuke Maruyama ◽  
Tetsuya Higashiyama
Keyword(s):  


Development ◽  
2016 ◽  
Vol 143 (15) ◽  
pp. 2780-2790 ◽  
Author(s):  
Marta Adelina Mendes ◽  
Rosalinda Fiorella Guerra ◽  
Beatrice Castelnovo ◽  
Yuriria Silva-Velazquez ◽  
Piero Morandini ◽  
...  
Keyword(s):  


2016 ◽  
Vol 28 (5) ◽  
pp. 1035-1052 ◽  
Author(s):  
Xunliang Liu ◽  
Claudia Castro ◽  
Yanbing Wang ◽  
Jennifer Noble ◽  
Nathaniel Ponvert ◽  
...  


2014 ◽  
Vol 42 (2) ◽  
pp. 401-407 ◽  
Author(s):  
Stefanie Sprunck ◽  
Thomas Hackenberg ◽  
Maria Englhart ◽  
Frank Vogler

During double fertilization in Arabidopsis thaliana, the egg cell secretes small cysteine-rich EC1 (egg cell 1) proteins, which enable the arriving sperm pair to rapidly interact with the two female gametes. EC1 proteins are members of the large and unexplored group of ECA1 (early culture abundant 1) gametogenesis-related family proteins, characterized by a prolamin-like domain with six conserved cysteine residues that may form three pairs of disulfide bonds. The distinguishing marks of egg-cell-expressed EC1 proteins are, however, two short amino acid sequence motifs present in all EC1-like proteins. EC1 genes appear to encode the major CRPs (cysteine-rich proteins) expressed by the plant egg cell, and they are restricted to flowering plants, including the most basal extant flowering plant Amborella trichopoda. Many other ECA1 gametogenesis-related family genes are preferentially expressed in the synergid cell. Functional diversification among the ECA1 gametogenesis-related family is suggested by the different patterns of expression in the female gametophyte and the low primary sequence conservation.



2013 ◽  
Vol 26 (2) ◽  
pp. 93-99 ◽  
Author(s):  
Yehoram Leshem ◽  
Cameron Johnson ◽  
Venkatesan Sundaresan


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