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Postdoctoral Positions — Neural crest stem cells, pigment pattern, adult form

Posted by , on 1 June 2018

Closing Date: 15 March 2021

Postdoctoral positions are available in the Parichy lab at University of Virginia. The lab studies development using zebrafish and related species. Current emphases include hormonal control over post-embryonic neural crest stem cells, plasticity in cell state, evolution of novel cell types, and mechanisms of pattern formation and cell–cell communication within zebrafish and across Danio species.
Methods include super-resolution time-lapse imaging on lab-dedicated microscopes, single cell RNA-sequencing, forward and reverse genetics, conditional manipulation of gene activity, and others.
Examples of recent work include:
The Parichy lab is situated in a highly interactive department with state-of-the-art facilities and UVA has outstanding current and historical strengths in morphogenesis and pattern formation. Training environment is excellent.
Applicants must have or be pursuing a Ph.D. and must have experience with modern methods of developmental biology. Prior experience with zebrafish is not required.
Applicants should submit the following to Dr. David Parichy (dparichy@virginia.edu):
• CV
• contact information for three references
• brief description of interests, experience and career goals
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Student and PostDoc events at the BSDB Spring meeting 2018

Posted by , on 31 May 2018

At the 2018 Spring Meeting in Warwick, the PhD and PostDoc representatives organises a series of events for young researchers. These ranged from asking questions such as “What is the secret to success?” through to some crafty synthetic biology and ending with the award of the 2018 BSDB writing competition.

A huge thanks to Michelle Ware and Alexandra Ashcroft for all their work in organising BSDB events for young researchers over the years. Learn more about the incoming PhD and PostDoc representatives of the BSDB here.

 

Career workshop

The career workshop kicked off the BSDB 70th birthday celebrations, with a topic focused on ‘building resilience and overcoming obstacles’. The idea was to utilise the knowledge and experience of the successful developmental biologists attending the meeting to give plenary and session talks. In total we had 18 tables, lead by Ottoline Leyser, Jordan Raff, Robb Krumlauf, Maria Leptin, Steve Wilson, Matthew Freeman, Fiona Watt, Magdalena Zernicka-Goetz, Jan Traas, Judith Kimble, Henrik Semb, Anne Ferguson-Smith, Patrick Lamaire, Jean Paul Vincent, Kate Storey, Austin Smith and Yohanns Belliache.

We wanted to have honest and open discussions about how to succeed in academia. ‘What is the secret to success, if there is any?!’. It is not very often you get to have opportunity to pick the brains of the leaders in your area of interests. This led to an afternoon of lively discussions.

 

 

 

 

Student/postdoc social

The format of the last couple of student/postdoc socials have been designed to get people to interact with people other than their lab mates! This year was no exception. This year’s activity was for randomly assigned teams to build models, within 1 hour, of any one of the following themes: fertilisation, plant development, somitogenesis, cell-fate determination and evo-devo.  

We will let the pictures do the talking, but we were blown away by how amazing the models were and how much effort people put into making them. Megan Davey and Rita Sousa-Nunes judged the competition but had a hard time choosing winners since the models were excellent.

We are grateful to all the exhibitors who kindly donated prizes: Abcam, Class Learning, Proteintech, Philosophical Transactions B and Biographical Memoirs, The Company of Biologists, Stratech, 2BScientific and Indigo Scientific.

 

 

 

2018 BSDB Writing Competition

Finally, the student/postdoc events ended with the announcement of the 2018 Writing Competition. As part of the BSDB 70th anniversary celebrations, we initiated a writing competition where first prize was

a trip to the 77th Annual Society of Developmental Biology meeting (Portland, Oregon, USA). Katherine Brown, Aidan Maartens, Ottoline Leyser and Jonathan Slack judged the competition, selecting Daniyal Jafree as the winner.

 

So this year, is the final year for us organising these events. It has been a blast. Thank you all for making it such a wonderful and memorable experience. Please don’t forget to contact your future student (students@bsdb.org) or postdoc (postdocs@bsdb.org) reps for any comments or suggestions regarding the British developmental biology community.

 

See here for more pictures of the student/postdoc events.

 

Michelle and Alex

 

 

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Visualizing data with R/ggplot2 – It’s about time

Posted by , on 31 May 2018

The visualization of temporal data by line graphs has been documented and popularized by William Playfair in the 18th century (Aigner et al, 2011Beniger and Robyn, 1978). Today, time-dependent changes are still depicted by line graphs and ideally accompanied by a measure of uncertainty (Marx, 2013). Below, I provide a ‘walk-through’ for generating such a plot with R/ggplot2 to visualize data from time-series. For convenience, example data and an R-script that performs all steps is available here. The data that I used is from Mastop et al (2017). After the make-over with ggplot2, the graph looks like this:

 

Some time ago, my favorite (commercial) software package for making graphs was no longer supported due to a system upgrade. So I was looking for a powerful and flexible alternative for data visualization. I ended up with R and ggplot2. First of all, the elegant data visualization delivered by the ggplot2 package is hard to beat. On top of that, it is completely free and it has a large user base. The biggest obstacle (in my experience) was getting used to the tidy data format that is needed as input. The conversion of ordinary, spreadsheet type data into long, tidy data is dealt with in a previous blog, and again briefly explained below. Before we start, we need to load two packages (these need to be installed first):

>require(tidyr)
>require(ggplot2)

The example data (available here) is read from a file in csv format into a dataframe (you need to set the “working directory” to match the location of the file):

>df_wide <- read.csv("FRET-ratio-wide.csv", na.strings = "")

To find out wat the first six rows of the dataframe look like type:

>head(df_wide)

which returns:

  Time    cell.1    cell.2    cell.3    cell.4 ...   cell.12
1    0 0.9935818 0.9965762 0.9907055 0.9938881 ... 0.9859260
2    2 0.9972606 0.9979417 1.0014600 1.0041020 ... 1.0080610
3    4 1.0109350 1.0076620 1.0023690 1.0011580 ... 0.9993525
4    6 0.9959134 1.0018910 1.0034930 1.0011640 ... 0.9900663
5    8 0.9970548 0.9971041 0.9957852 1.0019420 ... 0.9979293
6   10 1.0038560 1.0018550 0.9897691 0.9976327 ... 1.0042090

The first column defines time and the other columns have data of individual cells corresponding to each of the timepoints. This data has a spreadsheet format, which is also named a ‘wide’ format. The first step is to convert it into a tidy data format, which is ‘long’. For details see my previous blog. The command to convert the df_wide dataframe into a tidy dataframe, df_tidy, is:

>df_tidy <- gather(df_wide, Cell, Ratio, -Time)

You can have a look at the first six rows of the dataframe to see what has changed:

>head(df_tidy)

 

Generating a basic graph

Once the data in the df_tidy dataframe is in long/tidy format, it can be used to generate a graph. The minimal instructions needed to display a graph are:

  • The dataframe that is used as input: df_tidy
  • The data used for the x-axis: Time
  • The data used for the y-axis: Ratio

To plot the data with minimal instructions use the function qplot():

>qplot(data=df_tidy, x=Time, y=Ratio)

Points/dots are used by default, but for these data lines are more appropriate:

>qplot(data=df_tidy, x=Time, y=Ratio, geom='line')

In the resulting graph all the datapoints are connected by lines, and the curves are not grouped per cell. To imrove this use:

>qplot(data=df_tidy, x=Time, y=Ratio, geom='line', group=Cell)

Or goup the data per cell and give the data from each cell a different color:

>qplot(data=df_tidy, x=Time, y=Ratio, geom='line', color=Cell)

Generating a graph with layers

The ‘qplot’ command provides a quick way to plot the data. To have a bit more control we turn to ggplot2(). The syntax is slightly more complex, but it allows to plot multiple layers. To reproduce what was done with qplot we need:

>ggplot(df_tidy, aes(x=Time, y=Ratio)) + geom_line(aes(color=Cell))

The aes() function is used for mapping “aesthetics”.  The aesthetics specify how the variables from the dataframe are used to visualise those variables. In this case ‘Time’ is used for mapping the data onto the x-axis and ‘Ratio’ is used to map the data onto the y-axis. The geom_line() function specifies that the data is shown as a line. Inside geom_line(), aes(color=Cell) specifies that the line of each cell is mapped to a unique color. For more information on aesthetics and examples see this book chapter.

The geom_line() function defines that the data are displayed as lines. We can add another layer with a different geometric shape, geom_point(), to show the individual data as dots (in this example the dots will not have a color, since no aesthetic mapping is specified for geom_point):

>ggplot(df_tidy, aes(x=Time, y=Ratio))+ geom_line(aes(color=Cell))+ geom_point()

The thickness of the lines and the size of the dots (size) and transparency of the dots (alpha) can be adjusted, for example:

>ggplot(df_tidy, aes(x=Time, y=Ratio)) + geom_line(aes(color=Cell), size=0.8) +
  geom_point(size = 1, alpha=0.3)

The appearance of the plot depends on the sequence in which the layers are added. This is defined by the sequence in which the objects are added, i.e. the first object defines the first layer and next object is added on top. For instance, this code will generate a plot in which the lines are on top of the points:

> ggplot(df_tidy, aes(x=Time, y=Ratio)) + geom_point(alpha=0.3, size=0.5) +
   geom_line(aes(color=Cell), size=0.8)

To generate a plot in which the points are visible, we define them as the last object and hence, they are added on top of the lines:

>ggplot(df_tidy, aes(x=Time, y=Ratio)) + geom_line(aes(color=Cell), size=0.8) +
   geom_point(alpha=0.3, size=0.5)

Generating a graph with data summaries

The option of adding layers allows the addition of a summary of the data, for instance the average, or data for various types of error bars. To achieve this, a dataframe is defined to store the summary statistics:

>df_summary <- data.frame(Time=df_wide$Time, n=tapply(df_tidy$Ratio, df_tidy$Time, length), mean=tapply(df_tidy$Ratio, df_tidy$Time, mean))

This will generate a df_summary dataframe that has the average signal and the number of samples per time point.

To add the standard deviation and standard error of the mean:

> df_summary$sd <- tapply(df_tidy$Ratio, df_tidy$Time, sd)

> df_summary$sem <- df_summary$sd/sqrt(df_summary$n-1)
> head(df_summary)

Returns:

   Time  n      mean          sd          sem
0     0 12 0.9929529 0.003313210 0.0009989706
2     2 12 0.9989194 0.007343436 0.0022141294
4     4 12 1.0027538 0.004194419 0.0012646648
6     6 12 1.0002915 0.006014562 0.0018134585
8     8 12 0.9994599 0.002606858 0.0007859971
10   10 12 1.0007186 0.004189333 0.0012631315

Finally, we add the lower and upper bound of the 95% confidence interval:

>df_summary$CI_lower <- df_summary$mean + qt((1-0.95)/2, df=df_summary$n-1)*df_summary$sem
>df_summary$CI_upper <- df_summary$mean - qt((1-0.95)/2, df=df_summary$n-1)*df_summary$sem

We can start by plotting the average response:

>ggplot(df_summary, aes(x=Time, y=mean)) +
   geom_line(data=df_summary, aes(x=Time, y=mean), size=1, alpha=0.8)

We add the 95% confidence interval (95%CI) as a measure of uncertainty. Here we employ geom_ribbon() to draw a band that captures the 95%CI. To this end, we employ aes() inside geom_ribbon() to specify that the upper and lower limits of the confidence interval from df_summary define the borders of the ribbon. (Note that alternative methods that display uncertainty may be considered.)

>ggplot(df_summary, aes(x=Time, y=mean)) +
   geom_line(size=1, alpha=0.8) +
   geom_ribbon(aes(ymin=CI_lower, ymax=CI_upper) ,fill="blue", alpha=0.2)

The resulting figure only shows the data summary. Since it can be valuable to show the underlying data we will plot the data from individual cells as well. These data are present in another dataframe, yet it is possible to add these data to another layer. To demonstrate this, the original data from the individual measurements (from df_tidy) is added:

>ggplot(df_summary, aes(x=Time, y=mean)) +
   geom_line(size=1, alpha=0.8) +
   geom_ribbon(aes(ymin=CI_lower, ymax=CI_upper), fill="blue", alpha=0.2) +
   geom_line(data=df_tidy, aes(x=Time, y=Ratio, group=Cell))

Improving the presentation and annotation of the graph

The graph shown above displays all the data of interest, but it looks cluttered. In the final session the lay-out and annotation will be changed to improve the visualization and communication of the results (see also ‘Graphics for Communication’).

To make the individual data less pronounced, the lines are plotted in grey. Also, the graph looks better if the ribbon of the 95%CI is drawn on top, so we move the grey lines to the first layer and plot the average and 95%CI on top of that:

>ggplot(df_summary, aes(x=Time, y=mean)) +
   geom_line(data=df_tidy, aes(x=Time, y=Ratio, group=Cell), color="grey") +
   geom_line(size=1, alpha=0.8) +
   geom_ribbon(aes(ymin=CI_lower, ymax=CI_upper) ,fill="blue", alpha=0.2)

To indicate where we performed a manipulation of the system another layer can be added. In this experiment a stimulus was added at t=44 and inhibited at t=146. To reflect this, we add a grey box with the function annotate():

>ggplot(df_summary, aes(x=Time, y=mean)) +
   geom_line(data=df_tidy, aes(x=Time, y=Ratio, group=Cell), color="grey") +
   geom_line(size=1, alpha=0.8) +
   geom_ribbon(aes(ymin=CI_lower, ymax=CI_upper) ,fill="blue", alpha=0.2) +
   annotate("rect",xmin=44,xmax=146,ymin=-Inf,ymax=Inf, alpha=0.1, fill="black")

To change the default grey background from the area of the graph, the ‘theme’ can be changed:

>ggplot(df_summary, aes(x=Time, y=mean)) +
   geom_line(data=df_tidy, aes(x=Time, y=Ratio, group=Cell), color="grey") +
   geom_line(size=1, alpha=0.8) +
   geom_ribbon(aes(ymin=CI_lower, ymax=CI_upper) ,fill="blue", alpha=0.2) +
   annotate("rect",xmin=44,xmax=146,ymin=-Inf,ymax=Inf,alpha=0.1,fill="black")+
   theme_light(base_size = 16)

Finally, we change the labels of the x- and y-axis and add a title:

>ggplot(df_summary, aes(x=Time, y=mean)) +
   geom_line(data=df_tidy, aes(x=Time, y=Ratio, group=Cell), color="grey") +
   geom_line(size=1, alpha=0.8) +
   geom_ribbon(aes(ymin=CI_lower, ymax=CI_upper) ,fill="blue", alpha=0.2) +
   annotate("rect",xmin=44,xmax=146,ymin=-Inf,ymax=Inf,alpha=0.1,fill="black") +
   theme_light(base_size = 16) +
   ylab("Ratio YFP/CFP [-]") + xlab("Time [s]") +
   ggtitle("G-protein activation by histamine")

Final words

The end results is a nice and clean visualization of the data, which is an improvement over the original visualization (made with commercial software, see insets of figure 6 from Mastop et al (2017)). The instruction to plot graphs with ggplot() usually consists of several different functions and may be daunting at first sight. I hope that providing this ‘walk-through’ that shows how to build a graph layer-by-layer lowers the barrier to start using R/ggplot2 for visualization of (temporal) data.

 

Acknowledgments: Thanks to Franka van der Linden, Eike Mahlandt and Jenny Olins for testing and debugging the code.

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Categories: Education, Research

Royal Society PhD Studentship (4 Years)

Posted by , on 31 May 2018

Closing Date: 15 March 2021

Applications are invited for a four year PhD studentship funded by The Royal Society to conduct research under the supervision of Dr Amanda Sferruzzi-Perri at the Department of Physiology, Development and Neuroscience.

Title: Role of placental endocrine malfunction in the programming of disease in offspring

Closing date: 17th June 2018

For more details about the project and application process please see the following webpage:

http://www.jobs.cam.ac.uk/job/17502/

 

 

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The Novo Nordisk Foundation Center for Stem Cell Biology (DanStem) offers a postdoc position in Human Pluripotent Stem Cell-based Cell Therapy in Type 1 Diabetes

Posted by , on 31 May 2018

Closing Date: 15 March 2021

DanStem is looking for a postdoctoral candidate with a strong cell biological and cell signaling background in directed differentiation of human pluripotent stem cell biology.

The candidate is expected to work on the engineering of human pluripotent stem cell-derived islet of Langerhans-like aggregates with functional properties close to human islets. The functionality and therapeutic potential of the aggregates will be tested in vitro and in vivo in mice.
The goal of this project is to engineer therapeutically active islet-like aggregates for future cell therapy phase 1 trials in Type 1 Diabetes (T1D).
The candidate is expected to use state-of-the-art genetics, molecular and cell biological, and tissue engineering experimental strategies. The candidate will work together with a dedicated team of scientists and technicians who together will tackle bottle-necks towards implementing the phase 1 clinical trials in T1D.
Qualifications: 
The candidate is required to hold a PhD degree in pluripotent stem cell/developmental biology. A few years of postdoctoral experience in the same areas is a merit. The candidate should also have hands on experience in human pluripotent stem cell maintenance and differentiation, 3D culture of pluripotent stem cells, various cell and molecular biological methods, flow cytometry and live-cell imaging. Experience in differentiation towards pancreatic lineages is a merit. Finally, we are looking for applicants with a good record of peer reviewed scientific publications, grant writing skills and an interest in team work.
About our center:  
The Novo Nordisk Foundation Center for Stem Cell Biology – DanStem – addresses basic research questions in stem cell and developmental biology and translates results from basic research into new strategies and targets for the development of new therapies for diabetes and cancer. DanStem was established as a result of a series of international recruitments coupled with internationally recognized research groups focused on insulin producing beta cells and cancer research already located at the University of Copenhagen.
Find more information about the Center at https://danstem.ku.dk/
Employment Conditions:
The position is for 2 years with a possible extension. The employment is planned to start as soon as possible or upon agreement.
The terms of employment are set according to the Agreement between the Ministry of Finance and The Danish Confederation of Professional Associations or other relevant professional organization. The position will be at the level of postdoctoral fellow and the basic salary according to seniority is 32.700-34.400 DKK/month. A supplement could be negotiated, dependent on the candidate´s experiences and qualifications. In addition, a monthly contribution of 17.1% of the salary is paid into a pension fund.
Applicants recruited from abroad may be eligible for a special researcher taxation scheme. In all cases, the ability to perform the job will be the primary consideration, and thus we encourage all – regardless of their personal background and status – to apply.
For further information, please contact Professor Henrik Semb, henrik.semb@sund.ku.dk
International applicants may find the following links useful: UCHP’s international dept. ISM on https://ism.ku.dk/  and Work In Denmark on https://www.workindenmark.dk/
Application: 
The application must be submitted online and in English, by clicking on “Apply online” below.
 
The closing date for applications is July 15th 2018 at 23.59pm.   
The application must include:
  • Cover letter detailing the basis on which the applicant scientific qualifications meet the requirements for this position.
  • Curriculum vitae.
  • List of references (full address, incl. email and phone number)
  • Diplomas – all relevant certificates.
  • List of publications.
The further process:  
After the expiry of the deadline for applications, the authorized recruitment manager selects applicants for assessment on the advice of the Appointments Committee. All applicants are then immediately notified whether their application has been passed for assessment by an expert assessment committee. Selected applicants are notified of the composition of the committee and each applicant has the opportunity to comment on his/her assessment. You may read about the recruitment process on
DanStem and The University of Copenhagen wish to reflect the diversity of society and welcome applications from all qualified candidates, regardless of personal background 

APPLY NOW

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Categories: Jobs

Masters (Mgr) & Ph.D. level studentships in preimplantation mouse embryo development

Posted by , on 30 May 2018

Closing Date: 15 March 2021

The Laboratory of Early Mammalian Developmental Biology (LEMDB), University of South Bohemia, České Budějovice, Czech Republic (Alexander W. Bruce group).

The LEMDB is currently recruiting both Masters (Mgr) & Ph.D. level studentships to research projects related to cell-fate choice.

Research projects offered in relation to p38 mitogen-activated-kinase’s role in primitive endoderm/ PrE development, the regulation of spatial allocation of cells relevant to first differential cell-fates i.e. outer trophectoderm/TE & inner-cell-mass/ ICM and others…

University provided stipend guaranteed for 4-years (plus grant based salaries and performance related bonuses)

Please send your CV and covering letters to lab head Alexander W. Bruce at: awbruce@prf.jcu.cz

FaceBook: LEMDB facebook

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From stem cells to human development – early bird deadline approaching!

Posted by , on 30 May 2018

In September, Development is hosting the third of its highly successful series of meetings focusing on human developmental biology. Held in the Wotton House estate near Dorking in Surrey and organised by Paola ArlottaAli BrivanlouOlivier Pourquié and Jason Spence, the meeting will cover the latest developments and future prospects for this rapidly evolving field.

 

 

The early bird deadline is Thursday, 31st of May!

 

Find out more and apply here:

biologists.com/meetings/from-stem-cells-to-human-development-september-2018

 

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Categories: Events

Postdoctoral position on the robustness of neuronal specification programs at the Developmental Biology Institute in Marseille

Posted by , on 28 May 2018

Closing Date: 15 March 2021

A postdoctoral position is available starting in October 2018 at the Developmental Biology Institute of Marseille, France, located on the Luminy campus, in the group of Vincent Bertrand. The position is funded for 3 years.

The acquisition and maintenance of the differentiated state of a neuron are achieved by terminal transcription factors that are expressed throughout the life of the neurons. However, gene expression is often noisy, presenting a high stochastic variability. The objective of this project is to determine how the identity of a neuron can be established and maintained throughout the life of the animal in a reliable manner despite this variability. This question will be addressed using C. elegans, an excellent system to analyze the robustness of neuronal development. The project will combine recent genome engineering methods (CRISPR), quantitative in vivo imaging and single molecule FISH.

We are seeking a highly motivated candidate with a PhD in molecular biology, genetics, cell biology, developmental biology or neurobiology. The working language in the laboratory is English.

A letter of motivation, a CV and the names of two referees should be sent to Vincent Bertrand (vincent.bertrand@univ-amu.fr).

The announcement on IBDM website here.

 

 

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Categories: Jobs

Postdoctoral Position in Cardiovascular Development and Congenital Heart Disease

Posted by , on 25 May 2018

Closing Date: 15 March 2021

A postdoctoral position is available in the laboratory of Dr. Sophie Astrof at Thomas Jefferson University to study roles of cell-extracellular matrix (ECM) interactions in cardiovascular development and congenital heart disease. We have recently discovered that progenitors within the second heart field (SHF) give rise to endothelial cells composing pharyngeal arch arteries. Projects in the lab focus on the role of ECM in regulating the development of SHF-derived progenitors into endothelial cells and their morphogenesis into blood vessels. The successful candidate will combine genetic manipulation, embryology, cell biology, and confocal imaging to study molecular mechanisms of micro-environmental sensing during vascular development.
Astrof laboratory is a part of a modern and well-equipped Center for Translational Medicine at Jefferson Medical College (http://www.jefferson.edu/university/research/researcher/researcher-faculty/astrof-laboratory.html) located in the heart of Philadelphia.
To apply, please send a letter of interest detailing your expertise, CV and names and contact information of three references to sophie.astrof@gmail.com

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The people behind the papers – Pauline Anne & Christian Hardtke

Posted by , on 25 May 2018

Short CLE peptides regulate a wide variety of processes during plant development. In the developing root, the receptors and co-receptors for CLEs have remained largely unclear, as have the relationships between different CLEs and different (co-)receptors. A new paper in Development addresses this problem by reporting a new receptor kinase involved in CLE signaling. We caught up with lead author Pauline Anne and her PI Christian Hardtke, Professor in the Department of Plant Molecular Biology at University of Lausanne, to find out more.

 

 

Christian, can you give us your scientific biography and the questions your lab is trying to answer?

Out of an early interest in genetics, I studied Biology at the University of Munich. I became particularly fascinated by Developmental Biology when I learned about the then still recent isolation of the Bicoid morphogen. At that point I was determined to work with Drosophila. Incidentally, Thomas Berleth, who had cloned Bicoid a few years earlier, worked with Gerd Juergens in the Genetics department at that time. They were recruiting an M.Sc. student to investigate the “Arabidopsis embryo patterning mutant monopteros”. I only realised during the interview that Arabidopsis was not some short germ-band insect, but an upcoming plant model organism. Maybe my judgement was clouded by the dense pipe smoke in Gerd’s office, but I committed to the project, which also became my Ph.D. In hindsight, it was a stroke of luck, I enjoy working with plants ever since.
Four years later I had cloned MONOPTEROS and walked enough along chromosomes. Thus, after briefly wrapping up my Ph.D. work at the University of Toronto with Thomas, I started my postdoc as an HFSP fellow in the lab of Xing-Wang Deng at Yale University, to learn biochemistry. It was an exciting time as the lab discovered the mechanistic basis of the COP9-COP1 signalosome-ubiquitin ligase system in Arabidopsis photomorphogenesis, and its operational conservation but differential output in distant eukaryotes. When I started my own lab at McGill University however, I turned to root system architecture with the aim to analyse its intraspecific natural genetic variation. Since then, we isolated several QTL alleles. Because I like to explore the molecular foundations of their developmental phenotypes, my lab’s focus has shifted in the years after I moved to the University of Lausanne. Nowadays we are mainly interested in deciphering molecular pathways that govern the patterned differentiation of plant vascular tissues, and in identifying the non-cell autonomous signals that are emitted from phloem vasculature to organize surrounding tissues.

And Pauline, how did you come to work in Christian’s lab and be involved with this project?

Christian and I share common interests. In my PhD, I characterised the phloem regulator OCTOPUS (OPS) and its interaction with the brassinosteroid phytohormone pathway. I wanted to continue working on phloem differentiation, and Christian is a leader in that field. We discussed possibilities, I wanted to continue exploring signalling pathways, so he proposed to analyse CLE26 sensing, which we suspected to play a role in phloem differentiation.

 

When did your lab first get interested in CLE peptide signalling in the root?

CH When we got stuck in our analysis of BREVIS RADIX (BRX), another positive regulator of phloem formation. Stephen Depuydt, a postdoc in my lab at the time, proposed to screen for suppressors of the phloem defects in brx mutants. Although I was rather sceptical about the prospect of healing the strong brx phenotype by second site mutation.
PA But it worked! Loss-of-function in BARELY ANY MERISTEM 3 (BAM3), a receptor kinase, was isolated as a perfect brx suppressor from this screen. They later found that BAM3 is the receptor for the phloem-specific CLE45 peptide, pointing to a role of autocrine CLE peptide signalling in phloem differentiation.

 

CLERK expression pattern in seedlings from Fig. 3 in the paper

 

Can you give us the key results of the paper in a paragraph?

PA We isolated CLERK as a genetic component of CLE26 sensing in the root, but it is also required for perception of other CLE peptides. Moreover, CLERK encodes a co-receptor protein that acts in the phloem and is necessary to prevent premature protophloem specification.

CH Also, CLERK acts genetically in parallel to described CLE sensing pathways in the protophloem, corroborating the redundancy we suspected at the outset.

 

You have lots of CLE peptides, lots of receptors, lots of co-receptors, and lots of promiscuous receptor-ligand and receptor-co-receptor interactions. How does this system achieve any degree of specificity?

PA Although many exogenously applied CLE peptides suppress root protophloem differentiation, only few, like CLE45 or CLE26, are actually expressed in root development. Recent studies by colleagues suggest that some CLEs are induced by specific environmental stimuli, to shut down root growth in unfavourable conditions. So part of the answer probably lies in specific ligand expression.

CH …and in specific receptor and co-receptor expression. It is also noteworthy that some receptors are not only more promiscuous with respect to ligands than others, but that ligand binding affinities can vary by an order of magnitude. So even in presence of multiple receptor-coreceptor pairs, ligand interaction can likely trigger vastly different signal outputs. It will be a major challenge to map these interactions in time and space, also because cross-regulation between CLE-sensing receptors has been observed.

 

How might CLERK help you in future analysis of the CLE sensing pathway?

CH One surprising discovery was that in brx or ops mutants, CLERK is not required for CLE26 or CLE45 sensing. We can therefore perform a sensitized screen for CLE resistance, for example in a brx clerk double mutant background. This should enable us to home in on the CLE26 receptor, as well as receptors for other CLEs.

PA The system is more and more complex, and genetics does not always give the expected answers. But it looks like it is less complex in the root than in the shoot. For example, while our paper was under review, colleagues found that CLERK also plays a role in the shoot. However, there its action is masked by redundancy between four related co-receptors.

 

CLERK’s effects on CVP2 expression, from Fig. 5 in the paper

 

When doing the research, did you have any particular result or eureka moment that has stuck with you?

PA Yes, the day I received the whole genome sequencing results of our original clerk mutant! I was on vacation in Italy. As you guess, I could not wait to be back in the lab to analyse the results…and At2g23950 popped up, a receptor-like kinase. This was the best candidate I could expect at that moment.

 

And what about the flipside: any moments of frustration or despair?

PA Of course! Even if the project went well, there are more instances of frustration in research life than eureka moments. I think my main frustration was the very weak expression level of CLERK in the root tip. But on the upside, this forced me to hone my confocal microscopy skills…

What next for you after this paper?

PA In the short term, I will focus on the characterization of other candidates isolated from the screen. I am most interested in a downstream CLE signalling component that I isolated recently, a prey that the lab has long been after. In the long term, I hope to turn my projects into more publications, to be competitive in the academic job market.

And where will this work take the Hardtke lab?

CH It will force us deeper into investigating the mechanics of CLE perception. One unexpected result contributed by our collaborators, Michael Hothorn’s lab, was the observation that the CLERK ectodomain cannot interact with the ectodomains of a few known bona fide CLE receptors, in the presence of ligand. If CLERK is indeed a generic CLE co-receptor, which is a parsimonious assumption, then this indicates that something is missing to make the system work biochemically in isolation. Maybe the sensitized screen will deliver this piece of the puzzle.

 

Finally, let’s move outside the lab – what do you like to do in your spare time?

CH Depends on the time of year. In the winter, I take every opportunity to go skiing. Luckily, from Lausanne it only takes about one hour to reach the bottom of some of the most spectacular ski slopes on the planet. In the summer, I like to attend a random selection of sports events. In general, I like to watch people perform feats that are impossible for myself, like swimming 100 m in less than a minute…

PA …I am a mom of two young kids, 3 years and one and a half years old. I spend all my free time with them and I really enjoy it. I love to read books with them. But sometimes I also have to fold up to fit in a cardboard hut, to escape wolves or other monsters. Sometimes it is more tiring to be a mom than to be in the lab. But my favourite moments are with the kids outside, observing nature, playing with its treasures, showing them birds, insects and, of course, plants!


 

Pauline AnneAmelia Amiguet-VercherBenjamin BrandtLothar KalmbachNiko GeldnerMichael HothornChristian S. Hardtke
This is #43 in our interview series – check out the archive here.

 

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