Genetic evidence for essential calcium transporters in pollen growth and fertilization. Sabine Frietsch 1,3, Shawn M. Romanowsky 1,2, Morton Schiøtt 4,

Slides:



Advertisements
Similar presentations
Determining the roles of the BTB genes At2g04740, At4g08455, At1g04390, and At2g30600 in Arabidopsis thaliana growth and development. Brandon D. Blaisdell,
Advertisements

Human Cellular Physiology PHSI3004/3904 Secreted signals and synaptic transmission Dr Bill Phillips Dept of Physiology, Anderson Stuart Bldg Rm N348.
Plant fertilization and transgenic plants How does fertilization occur in plants? How do you make a transgenic plant?
Cell expansion plays a major role in growth Root cells expand their volume 50 times by expanding lengthwise but not widthwise.
Oscillations in Pollen Tube Growth & ROP Signaling Network Oscillations in Pollen Tube Growth & ROP Signaling Network XIA, Fan.
Plant fertilization and transgenic plants How does fertilization occur in plants? How do you make a transgenic plant?
Young Leaf Shoot Tip Axillary Bud Node Internode.
Arabidopsis Experiments Forward Genetic Screen (Ethylene Insensitive Mutants) Reverse Genetic Screen / PCR Genotyping (H + - ATPase Mutants)
Mutations in Arabidopsis Exocyst Gene AtSEC8 Jennie Hines Mentor: John Fowler.
Arabidopsis Experiments
Calcium Oscillation in the Pollen Tube Growth Presented by: XIA,Fan
Pollen Tube -- the model system for the study of cell polarity control and tip growth Speaker: Chunhui Cai.
Plant Molecular Genetics and Genetic Transformation HORT 301 – Plant Physiology November 1, 2010 Taiz and Zeiger – Chapter 2, Smith et al. (2010) – Chapter.
Testing a Role for Rop9 GTPase in Maize Pollen Tube Growth Lauren A. Osborn Dr. John Fowler Botany and Plant Pathology Summer 2005.
Plant Development PS452 Feng Chen 01/21/2014
Plant Reproduction BIOL /21/ /26/2008.
Katie Canul 1, Jeneva Foster 2, Christopher Wreden, PhD 2, and Karen Guillemin, PhD 2 1 California State University Monterey Bay, Seaside, CA 2, University.
Sergio Tonetto de Freitas and Elizabeth J. Mitcham Department of Plant Sciences, University of California, Davis, CA USA
Background Introduction By Bensen Fan Kristin Gill Maria Garcia.
Ca 2+ signaling in plant Light Cold stress Heat shock Mechanical stresses (Touch, wind & Wounding) Pathogen invading Phytohormones (Auxin, ABA, GA) Gravity.
Development of an Isolated, in Vitro C. elegans Gonad Preparation Adam Broslat Advisor: Dr. Kevin Strange Professor of Anesthesiology and Pharmacology.
Phenotypic Characterization of lrb Mutants in Arabidopsis thaliana. Brandon D. Blaisdell 1, Matthew Christians 2, Derek J. Gingerich 1 1 Department of.
Arabidopsis thaliana Response to Tobacco Rattle Virus Jessica Martin, Cory Zoetewey, and Lisa K. Johansen, Department of Biology University of Colorado.
Phosphorylation of the Tomato Β-Subunit of the SnRK Complex by Adi3 and its Possible Role in Sugar Signaling JULIAN AVILA-PACHECO.
Genetics Really about growth and development……. Heredity Heredity is biological inheritance –The set of characteristics an organism inherits form its.
Alkaline pH sensing in Candida albicans
The Critical Requirement for Linolenic Acid Is Pollen Development, Not Photosynthesis, in an Arabidopsis Mutant Michele McConn and John Browse Presentation.
Gene Nomenclature Budding Yeast: CDC28 = wild type gene cdc28 = recessive mutant allele Cdc28 or Cdc28p = CDC28 protein Fission Yeast: cdc2 = the wild.
Voltage-gated Ca 2+ Channels (VGCCs) For review, see: Catterall, Annu. Rev. Cell Dev. Biol. 16:
Supporting information Figs S1-S5. Figure s1 Histochemical assay of root H 2 O 2 All of roots from seedlings grown in MS or containing 20 µM ABA for 12.
PARTIAL LOSS OF TIP60 SLOWS MID-STAGE NEURODEGENERATION IN A SPINOCEREBELLAR ATAXIA TYPE 1 (SCA1) MOUSE MODEL -KRISTEN M. GEHRKING, J. MICHAEL ANDRESEN,
Wsmutant a b Fig. S1 Morphology of the low-iron-sensitive mutant of Arabidopsis. (a) Wild type (Ws) and the low-iron-sensitive mutant (mutant) germinated.
The Pollination Story Diversity of Life Grade 7. The Pollination Story  The ovary of the flower is where the seeds develop.
Characterization of gig1 (glucose insensitive growth 1) Reveals the Involvement of the Plastidic Copper Transporter PAA1 in Sugar-mediated Interorganellar.
Cell-cell communication during double fertilization
Fig. 2 Expression and subcellular localization of MSL8–GFP expressed from endogenous sequences. (A) Quantitative RT–PCR amplification of MSL8 transcripts.
Role of PICH (Plk-1 Interacting Checkpoint “Helicase”) in the Spindle Checkpoints of Plants Ron M. G. Menorca • Joe Ramahi • Pak Kwong • Ravi Maruthachalam.
Volume 25, Issue 11, Pages (June 2015)
Volume 41, Issue 6, Pages (March 2011)
Volume 29, Issue 4, Pages (May 2014)
PCS1 functions in gametogenesis and embryogenesis.
Volume 14, Issue 5, Pages (March 2004)
Volume 19, Issue 1, Pages (January 2016)
Volume 21, Issue 3, Pages (September 2011)
Annexin5 Is Essential for Pollen Development in Arabidopsis
Xiaochun Ge, Fang Chang, Hong Ma  Current Biology 
Volume 22, Issue 12, Pages (June 2012)
Transcriptional Activation of Arabidopsis Axis Patterning Genes WOX8/9 Links Zygote Polarity to Embryo Development  Minako Ueda, Zhongjuan Zhang, Thomas.
Volume 25, Issue 11, Pages (June 2015)
Volume 26, Issue 5, Pages (September 2013)
Double Fertilization in Arabidopsis thaliana Involves a Polyspermy Block on the Egg but Not the Central Cell  Scott Rod J. , Armstrong Susan J. , Doughty.
Volume 25, Issue 3, Pages (May 2013)
Lecture 2: Using Mutants to study Biological processes
Volume 1, Issue 4, Pages (July 2008)
Volume 6, Issue 4, Pages (July 2013)
Feng Yu, Wang Tian, Sheng Luan  Molecular Plant 
Volume 7, Issue 1, Pages (January 2014)
A DTX/MATE-Type Transporter Facilitates Abscisic Acid Efflux and Modulates ABA Sensitivity and Drought Tolerance in Arabidopsis  Haiwen Zhang, Huifen.
Volume 9, Issue 4, Pages (April 2016)
Volume 19, Issue 15, Pages (August 2009)
Volume 5, Issue 1, Pages (January 2012)
Volume 18, Issue 1, Pages (January 2008)
Maternal ENODLs Are Required for Pollen Tube Reception in Arabidopsis
Han-Wei Shih, Cody L. DePew, Nathan D. Miller, Gabriele B. Monshausen 
Plotting a Course Developmental Cell
Plant Fertilization: Bursting Pollen Tubes!
Volume 25, Issue 3, Pages (May 2013)
Kristin M. Beale, Alexander R. Leydon, Mark A. Johnson  Current Biology 
Volume 6, Issue 5, Pages (September 2013)
Volume 25, Issue 7, Pages e4 (November 2018)
Presentation transcript:

Genetic evidence for essential calcium transporters in pollen growth and fertilization. Sabine Frietsch 1,3, Shawn M. Romanowsky 1,2, Morton Schiøtt 4, Michael G. Palmgren 4, Jeffrey F. Harper 1,2 1 The Scripps Research Institute, Cell Biology, N. Torrey Pines Rd, La Jolla, CA, USA 2 University of Nevada, Biochemistry, 1664 North Virginia Str, Reno, CA, USA 3 University of California, San Diego, 9500 Gilman Drive, La Jolla, CA The Royal Veterinary and Agricultural University, Plant Biology, Thorvaldsensvej 40, DK-1871 Frederiksberg, Denmark and Introduction: Calcium dynamics are thought to play a central role in pollen development, as evidenced by pharmaco-chemical approaches and visualization of calcium gradients and oscillations. Using Arabidopsis as a model system, we provide the first genetic evidence to support a model in which calcium signals are natural regulators of pollen tube growth and fertilization. Calcium signals are largely controlled by influx (through channels) and efflux (through pumps and antiporters). We have identified T-DNA gene disruptions in all 14 calcium pumps, and all 20 cyclic nucleotide gated channels (CNGCs). From this set of mutants, distinct pollen specific phenotypes have been found for disruptions of ACA9 (a calmodulin activated plasma membrane calcium pump) and CNGC18 (a cyclic nucleotide and calmodulin regulated putative calcium channel). Calcium Pump Mutation aca9 Reduces Pollen Tube Growth Potential (in vivo) cngc18 -/+ have full seed set indicating that the defect is very different than the aca9 phenotype. Reciprocal crosses and out-crossing to the male sterile mutant, ms-1 show that cngc18 is male sterile. CONCLUSIONS: funiculus aca9 disruption results in partial male sterility WTaca9 Longest pollen tube Aniline blue stain WT ACA9promoter::GUS ACA9 appears to function as a plasma membrane pump in pollen aca9 disruption results in >50% reduced frequency of synergid penetration (discharge) required for fertilization aca9 -/- blocked fertilized Synergid penetration penetration / discharge Confocal image of GFP merged with DIC image No synergid pentration or sperm release Discharge + Discharge - Discharge +: Wild type 96% (n=178) aca9 41% (n=247) CNGC18 disruption results in complete male sterility No homozygous cngc18 in over 400 F1 progeny of two independent gene disruption lines. Homozygous gene disruption lines in all CNGCs but CNGC18. Alexander staining for pollen viability in the quartet background (qrt) shows that cngc18 pollen is normal developed and viable. Expression profile of CNGCs during pollen development Modified after Maeser et al., 2001 CNGC8 and CNGC18 are highly expressed in mature pollen. Only disruption of CNGC18 results in male sterility. 100x cngc18 pollen tubes germinate, but only grow a short distance, with a “kinky-like” non-directional growth, often prematurely terminating with a bursting event. cngc18 pollen germinate but has impaired tube growth in vitro 400x control, qrt (-/-)cngc18 (-/+), qrt (-/-) In vitro germination assays in the quartet background (pollen doesn’t separate during development). control, qrt (-/-) cngc18 (-/+), qrt (-/-) Working model for a CaM regulated calcium oscillator aca9 is the first mutant with a defect in pollen/ovule interaction. CNGC18 is the only CNGC essential for the plant life cycle. CNGC18 is the first potential calcium channel that was found to be involved in pollen tube growth. ACA9 and CNGC18 could be involve in a CaM regulated calcium oscillator, that is essential for pollen tube growth and fertilization. aca9 -/- plants display reduced pollen tube growth and >50% reduction of synergid penetration (discharge). ACA9: CNGC18: Model: cngc18 pollen germinates with underdeveloped, kinky pollen tubes, that often burst at the tip. Disruption of ACA9 results in partial male sterile plants with shorter siliques and reduced seed set. Disruption of CNGC18 results in complete male sterility. Honys and Twell, 2003, Extracted from NASC database WT,col cngc18 (-/+)