The community site for and by
developmental and stem cell biologists

Key protein in cilia assembly identified

Posted by , on 21 August 2015

The group led by ICREA Research Professor Cayetano Gonzalez at IRB Barcelona, in collaboration with the group of Professor Giuliano Callaini from the University of Siena in Italy, has published a new study in Current Biology that contributes to understanding how cilia are assembled.

Many cells in our bodies present a small structure that looks like, and as a matter of fact works as an antenna, conveying to the cell information on the extracellular environment. They are called cilia (plural) or cilium (singular). Ciliated cells play essential functions in the human body. Thus, for instance, the monitoring of fluid flow in the kidney, the detection of hormones in the brain, or the senses of hearing and smell depend on specialised neurons equipped with chemo-sensory or mechano-sensory cilia. Moreover, besides sensing, beating cilia keep fluids in motion in many parts of our bodies and are critical for human health.

A cilium can be regarded as a long and thin protrusion of the cell membrane that contains microtubules. Ciliary microtubules are arranged in a typical radial symmetry that is conserved through evolution and is templated by a small organelle that sits at the base of the cilium, known as basal body. Most animal cells contain two basal body-like structures (centrioles), but only one of them can actually work as basal body. In human cells, this is always the centriole that is said to be the “mother” because it was assembled earlier than the other, called the “daughter” centriole.

One laboratory animal model used to investigate how cilia are assembled is the vinegar fly Drosophila melanogaster. The article by the Gonzalez’s group shows that in Drosophila, as in humans, basal body fate is also reserved to the mother centriole. Moreover, through genetic manipulations that are easily performed in flies, they have been able to get a glimpse into the molecular mechanism that governs this fundamental process.

They have found that removal of the daughter-centriole specific protein Centrobin (CNB) allows daughter centrioles to serve as basal bodies. Thus CNB-depleted neurons present two cilia, the standard, which is templated by the mother centriole and a second one templated by the daughter centriole from which CNB has been removed. Conversely, mother centrioles engineered to carry CNB cannot function as basal bodies and, therefore, neurons modified this way cannot assemble cilia.

In humans, the lack of cilia, or cilia that do not work well, are the cause of a long list of disorders, known as ciliopathies, which include polydactyly, obesity, respiratory dysfunction, hearing impairment, and many others. Basic research in model organisms like the vinegar fly is helping to understand the molecular details of cilium assembly, thus paving the way to applied research in this field.

 

Reference article:

Loss of Centrobin enables daughter centrioles to form sensory cilia in Drosophila

M. Gottardo, G. Pollarolo, S. Llamazares, J. Reina, M. Riparbelli, G. Callaini, and C. Gonzalez

Current Biology (20 August) DOI: 10.1016/j.cub.2015.07.038

 

This article was first published on the 21st of August 2015 in the news section of the IRB Barcelona website

Thumbs up (No Ratings Yet)
Loading...

Tags: , , , ,
Categories: Research

Navigate the archive

Use our Advanced Search tool to search and filter posts by date, category, tags and authors.

Postdoctoral Research Associate

Posted by , on 20 August 2015

Closing Date: 15 March 2021

 

The Stowers Institute for Medical Research has two openings for postdoctoral researchers to work on projects using the cave fish system (Astyanax mexicanus) to address questions about the genetic basis of adaptation to new and extreme environments, with a particular focus on metabolic evolution.

Candidates will use RNA-sequencing, whole genome sequencing, transgenics, and metabolomics to uncover the genetic basis and underlying mechanism of the impressive metabolic adaptations cavefish have acquired to survive in nutrient poor environments.

Qualified candidates should have a background in evolutionary genetics and bioinformatics or a background in ecological genetics.  Research may be field-based, lab-based, or both.  Researchers who integrate genome level data with studies of ecology and evolution are encouraged to apply

One of the positions will involve substantial field work (in the caves in Mexico) to link the ecological settings in the caves with the observed and studied phenotypes.

Another position will direct the bioinformatics of the genomics of non-model organisms, and will analyze and interpret data accordingly.  Experience in handling large-scale sequence data is essential.

The ideal candidate has a doctorate degree in bioinformatics, genomics, or a related field; strong command of UNIX and other programming languages; hands-on experience with genomic data; and an interest in pursuing research on emerging model organisms.  In addition, the successful candidate will have a strong background in analysis of genetic and genomic data (e.g., whole-genome resequencing, RAD genotyping, QTL mapping) and/or experimental developmental biology (e.g., manipulation of gene expression, transgenesis, genome editing), and an ability and willingness to work both independently and collaboratively in a team-oriented environment.  No previous experience working with fish is required.

To apply, please submit a cover letter that includes a short summary of interests, a CV, and the contact information of 2-3 professional references to nro@stowers.org

Deadline for applications is September 15, 2015.  The positions are available October 1, 2015 (start date is flexible).
About the Stowers Institute for Medical Research

The Stowers Institute for Medical Research in Kansas City, Missouri* is a non-profit, basic biomedical research organization dedicated to improving human health by studying the fundamental processes of life.  Jim Stowers, founder of American Century Investments, and his wife, Virginia, opened the Institute in 2000.  Since then, the Institute has spent over 900 million dollars in pursuit of its mission.

Currently, the Institute is home to almost 550 researchers and support personnel; over 20 independent research programs; and more than a dozen technology-development and core facilities.  Kansas City is an emerging metropolitan city in the Midwest with a high quality of living and affordability.

*Visit https://www.visitkc.com for information about living and working in Kansas City.

Thumbs up (No Ratings Yet)
Loading...

Categories: Jobs

Useful databases and resources for developmental biologists

Posted by , on 20 August 2015

As you may have noticed, as part of our recent redesign we created a new Resources section on the site, which you can access via the menu bar. Within this section we have created three pages with links to websites that you may find useful:

 

Societies: links to national and international developmental biology societies

Databases

Other useful links: including bioinformatics, genomics and imaging tools, as well links to educational and outreach resources

 

These lists are not comprehensive, and this is where we need your help! Have we missed an important database? Is there a really useful tool that we should include? Is your national society not listed? Help us make these lists as relevant as possible to the developmental biology community by leaving your suggestions as a comment here, or via our contact form.

Thumbs up (No Ratings Yet)
Loading...

Categories: News, Resources

Pluripotent Stem Cell Platform Research Associate

Posted by , on 20 August 2015

Closing Date: 15 March 2021

Department/Location: Wellcome Trust – Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, UK

Salary: £28,695-£37,394

Reference: PS06912

Closing date: 20 September 2015

Fixed-term: The funds for this post are available until 31 January 2018 in the first instance.

The Pluripotent Stem Cell Platform (PSCP) is a hub in the UK Regenerative Medicine Platform, a joint research council programme to tackle the critical challenges in developing new regenerative treatments (www.ukrmp.org.uk). PSCP is a multi-disciplinary collaboration focussed on the quality controlled manufacturing and differentiation of human pluripotent stem cells suitable for clinical applications (http://www.ukrmp.org.uk/hubs/cell-behaviour-differentiation-and-manufacturing/).

A post-doctoral position is available for a PSCP project based in Cambridge under the direction of Roger Barker, Ludovic Vallier and Austin Smith at the Wellcome Trust-MRC Stem Cell Institute (www.stemcells.cam.ac.uk).

The research is centred on optimising the generation from human embryonic and induced pluripotent stem cells of neural derivatives suitable for development of cell based therapies, in particular midbrain dopaminergic neurons for Parkinson’s disease.

Candidates should have a PhD with experience in the culture and analysis of pluripotent stem cells or neural stem cells and/or neuronal differentiation and functional characterisation supported by relevant publications. Applications are encouraged from candidates with a translational focus and an appreciation of cell production requirements for clinical trials.

Technical support is available and access to a range of flow cytometry, imaging and qPCR instrumentation.

To apply online for this vacancy and to view further information about the role, please visit: http://www.jobs.cam.ac.uk/job/7926. This will take you to the role on the University’s Job Opportunities pages. There you will need to click on the ‘Apply online’ button and register an account with the University’s Web Recruitment System (if you have not already) and log in before completing the online application form.

The closing date for all applications is the Sunday 20 September 2015.

Please upload your Curriculum Vitae (CV) and a covering letter in the Upload section of the online application to supplement your application. If you upload any additional documents which have not been requested, we will not be able to consider these as part of your application.

Informal enquiries about the post are also welcome via email on jobs@stemcells.cam.ac.uk.

Interviews will be held week commencing 12 October 2015. If you have not been invited for interview by 9 October 2015, you have not been successful on this occasion.

Please quote reference PS06912 on your application and in any correspondence about this vacancy.

The University values diversity and is committed to equality of opportunity.

The University has a responsibility to ensure that all employees are eligible to live and work in the UK.

Thumbs up (No Ratings Yet)
Loading...

Categories: Jobs

Meeting Report: Pan-Am Evo-Devo’s first meeting

Posted by , on 19 August 2015

The inaugural meeting of the Pan-American Society for Evolutionary Developmental Biology took place from August 5th–9th at the Clark Kerr campus of UC Berkley, USA. Registration was full, with nearly 350 attendees, and excitement was in the air. An established researcher, Tamara Franz-Odendaal (Mount Saint Vincent University, Canada), and a graduate student, Allison Edgar (Duke University, USA), discuss the highlights:

TFO: It would be an understatement to say that there was lots of excitement and enthusiasm from all types of scientists.

AE: We all felt that buzz in the air! I think it was a celebration of how Evo-Devo bridges disciplines.

(more…)

Thumbs up (5 votes)
Loading...

Tags: , ,
Categories: Events

Visiting a collaborator’s lab? Apply for a travelling fellowship!

Posted by , on 19 August 2015

Are you a postdoc or student planning to visit a collaborator’s lab? Need help to offset your costs and expenses?

Then apply for a Development travelling fellowship! You can be awarded up to £2,500 (or currency equivalent), and there are no restrictions on nationality.

The next deadline for application is the 31st of August. For more information click here.

 

You can also find out more about the scheme, and how previous awardees have benefited from their visits, by reading their posts on the Node. Here are a few recent examples:

 

Finding Collaborators: from London to Stuttgart– by Rie Saba (postdoc in the UK) who visited the Schenke-Layland (Germany)

England, embryos, and axial columns: a Travelling Fellowship connecting Chicago to Cambridge– by Kate Criswell (PhD student in Chicago) who visited the Coates lab (UK)

Of mice and zebrafish– by Shauna Katz (PhD student in France) who visited the Guillemot lab (UK)

Development Travelling Fellowship: a node connecting Woods Hole with the Stowers Institute– by Alice Accorsi (PhD student in Italy) who visited the Sánchez Alvarado lab (USA)

Sweet Swiss…Zebrafish?!– by Monika Tomecka (PhD student in the UK) who visited the Mosimann lab (Switzerland).

Green eggs and serrano ham– by Mariana Delfino-Machin (lecturer in Costa Rica) who visited the Gómez-Skarmeta lab (Spain)

Learning to Inject Platynereis Embryos– by Maggie Pruitt (postdoc in the USA) who visited the Arendt lab (Germany)

Generation of Embryoid Bodies: a great tool to study vascular development– by Helena Serra (PhD student in Spain) who visited the Gerhardt lab (UK)

From a travel fellowship to starting your own lab– by Mirana Ramialison (postdoc in Australia) who visited the Furlong lab (Germany)

Rewiring the brain– by Sonia Sen (postdoc in India) who visited the Wang lab (USA)

 

TF2015

 

 

 

Thumbs up (1 votes)
Loading...

Categories: Funding, News

Postdoctoral position to study Wnt signaling and cell polarity

Posted by , on 18 August 2015

Closing Date: 15 March 2021

A postdoctoral position is available in the Sergei Sokol laboratory in the Department of Developmental and Regenerative Biology, Mount Sinai School of Medicine, New York, to study Wnt signaling and cell polarity in vertebrate embryos and mammalian progenitor cells. Another research project involves noncanonical mechanisms of neural crest development. See the description of our interests at http://research.mssm.edu/sokol/Sokol_lab/ .

 

Preference will be given to motivated applicants with strong background in molecular, cell or developmental biology, who published a first-author paper as a result of their graduate work. Interested candidates may send their CV, list of publications and three references to Dr. Sergei Sokol (sergei.sokol@mssm.edu).

Thumbs up (No Ratings Yet)
Loading...

Categories: Jobs

An interview with Caroline Dean

Posted by , on 18 August 2015

This interview first featured in Development.

 

Caroline Dean is a plant biologist based at the John Innes Centre in Norwich, UK. She helped to establish Arabidopsis as a model plant organism, and has worked for many years on the epigenetic mechanisms that regulate vernalisation, the process by which plants accelerate their flowering after periods of prolonged cold. We met Caroline at the recent Spring Meeting of the British Society for Developmental Biology. We asked her about her career, her thoughts on the plant field and being awarded this year’s FEBS EMBO Women in Science Award.

 

Caroline DeanWe are here at the Spring Meeting of the British Society for Developmental Biology. How are you finding the meeting?

This is not a meeting that I come to very often, but the questions asked here are always interesting because people think about my topic in a slightly different way. It’s always very interesting and illuminating to see what grabs people’s attention and what they get confused about.

 

This year you were awarded the FEBS EMBO Women in Science Award. What does receiving this prize mean to you, and what advice do you have for young female scientists?

I was thrilled to pieces! I heard on New Year’s Eve that I’d won it, so it was a great celebration that evening. It is a real honour because the women who have won this prize over the years are really fantastic scientists.

People have asked me how to encourage younger female scientists to break through the glass ceiling. There are still relatively few senior women scientists in Europe, although it’s not as bad as it used to be. My advice is to take the next obvious step at each stage of your career and not to worry too much about the long-term difficulties of a research career. When I started my career I didn’t have a clear goal, I didn’t aim to become a big leader in research. I just did research because I enjoyed it and found it an interesting topic. I really enjoyed being a graduate student and a postdoc, and now I really enjoy running a lab. So I would encourage young females to think “Yes, I can do it”, instead of worrying about “Well, can I achieve a work-life balance, can I compete in the current funding scenario, can I do this, can I do that?” I say to my postdocs “Jump, and then think!”

The nice thing about a science career is that it’s very flexible. As a PI you are your own boss, so if I needed to go off when the children were sick I did, and then caught up later. It’s not the type of job where you have to go in at set hours, so the flexibility helps enormously with the work-life balance. And children grow up very fast. There’s a lot of life left once they’ve left home!

 

Do you think role models, such as the women who have won this prize, are helpful?

I think role models do help. When I was a teenager my mother was the breadwinner, so for me the idea of a working mother was not unusual. At the John Innes Centre, I am involved in mentoring a number of project leaders and I also enjoy chatting to students and postdocs about research careers. I hope the younger scientists think “she managed to have a career and two kids who seem perfectly normal, and she is still quite into her science”, and that encourages them to continue.

 

How did you first become interested in biology? Was there someone who inspired you?

I loved the documentaries of the marine biologist Jacques Cousteau. I actually dragged my then boyfriend all the way down to Marseilles when I was 18 to see if I could meet him! Of course I didn’t, but I started off studying marine biology at university. I then discovered biochemistry, which I hadn’t really done at school. There was a particular plant biochemistry practical that I loved, where we isolated chloroplasts and did electron transport analysis. It really hooked me on lab work. I decided to be a technician so that I could continue doing lab work and after a year began a PhD – and it just rolled from there.

 

You did your undergraduate and PhD in the UK, but moved to California to do a postdoc in a biotech company. What was it like to work in industry?

The prospect of genetically modifying plants emerged when I finished my PhD, and venture capital funded a few start-up biotech companies. I did my postdoc in one of them, Advanced Genetic Sciences, in Oakland, California. The director, John Bedbrook (who came from academia), hired a bunch of academics. We had five years’ worth of money and our aim was to learn how to modify plants genetically and get foreign genes expressed in them. I learned all my molecular biology there. Very exciting times, because science was moving very quickly. So yes, it was a biotech company – but I could do fundamental academic research as part of the more biotech projects, e.g. generation of herbicide-tolerant plants. After five years, in 1988, I then moved back to the UK, to the John Innes Centre.

 

Your lab works on vernalisation. Why this scientific question?

When I was doing my postdoc in America, the Arabidopsis wave started – Elliot Meyerowitz and Chris Somerville initiated the use of a molecular genetic approach in Arabidopsis thaliana. I hadn’t done any such work while at the company, but I could see that this would open up analysis of really complex traits. For a trait like flowering time or developmental timing, we had no clue about which genes would be involved – you had to take a genetic approach. I chose to study vernalisation because of a conversation with a seller in a nursery garden in California. While I was buying some tulip bulbs he said to me “now put them in the fridge for six weeks before you plant them.” I was so intrigued that I looked it up: it turns out tulips need prolonged cold to flower in spring. I thought the whole ability of plants to monitor seasons was a really fascinating question. No one knew anything about molecular regulation of flowering time, let alone vernalisation, the acceleration of the flowering by cold that is very important for crop plants. Development of winter and spring varieties has significantly extended the geographical range of their production, but there was no molecular understanding of this trait. So I tackled that question using Arabidopsis genetics. I started this project in 1988 and we’re still doing it today!

We started off addressing different angles of the same question. Why do some plants need winter and others don’t? How does the plant actually remember that it has had winter? And how do plants cope with different lengths of winter? These research avenues all converged on a single regulator, a protein that blocks the transition to flowering: FLC. Whether you need winter or not depends on the expression level of that gene. Response to winter depends on epigenetically silencing that gene, and adaptation to different climates involves changes in that silencing mechanism.

The regulation of FLC involves conserved chromatin mechanisms, for example Polycomb silencing, and antisense RNAs. Subtle changes to the anti-sense transcripts are important to set the expression state, silence the gene or adapt to a different type of winter. It is a good system to understand the integration of many different layers of epigenetic regulation, which are often quite hard to dissect in other systems.

 

What are the next scientific questions that you would like to tackle?

I was lucky to be awarded a European Research Council grant to study how plants monitor and integrate fluctuating winter temperature. Plants integrate temperature changes over several weeks in order to monitor seasonal progression. I want to understand how they do that. What are the actual molecular thermosensors and how is their action channelled and integrated to regulate this one gene? We also want to understand how this process changes as plants adapt to different climates. These questions will be our focus over the next five years.

 

How has the use of Arabidopsis as a model system changed during your career?

Within the Arabidopsis community, there has been the development of very many extremely useful resources: genome sequences of 1000 natural accessions (there is a whole generation of students and postdocs that can’t remember what it was like doing science without a full genome sequence!); T-DNA collections knocking out all genes… Analysis of complex traits is now much faster in Arabidopsis. The scale of the international community also means you find things out by serendipity: you might think of a gene as flowering-specific and then find its mutation has been found in a completely different screen, which allows you to think of its function in a completely different way.

We need to fight the move for funders to think “let’s fund this reference plant for a bit, get the information we need and then concentrate on crop plants”. For example, flowering time is regulated by a variety of inputs: vernalisation, photoperiodicity, ambient temperature, metabolic signals. We are really quite a long way from understanding how all these fit together. We need to keep funding the basics to improve most rapidly our understanding of this complex adaptive trait – if we focus on flowering analysis in a few reference plants we will then be able to interpret experimental data on flowering in other species much faster. Gerry Fink, a yeast geneticist with an interest in Arabidopsis, made a very controversial statement in 1990: “If you want to understand wheat you should work on Arabidopsis, because four years of work on Arabidopsis will tell us more about wheat than working on wheat for four years.” We are still at the stage where it is very important to aim at a full understanding of how a whole plant works, responds to the environment and adapts. This is best done in reference plant systems at the same time as aiming to effectively translate this information into plant and crop biology as a whole.

 

At broad developmental biology meetings like this, there’s generally a very low representation of plant science. Would you like to see better integration between the plant and animal fields?

Plant science shouldn’t be seen as a poor relation. We should be very proud of what plant biology has contributed. If you look back at the history of biology, really fundamental discoveries – such as the concept of genetics, chromosomes, transposable elements, heterochromatin, small RNAs – have come from the plant field. Plant science should always be integrated into mainline biology. For example, our work has broad appeal because, although we are looking at a very plant-specific process, we have ended up studying epigenetic pathways that are widely conserved in eukaryotes. However, and this is true of many other communities, plant scientists tend to attend plant-specific meetings and publish in plant-specific journals, and this isolates them. I think it is good to reach beyond your own field. But fields operate using different languages, and this jargon (like the species-specific gene names) complicates comparisons. This is why it is quite good to have joint sessions as in this meeting.

 

What would people be surprised to find out about you?

I used to sail a lot before my children were born, but in the last few years my life has been a mosaic of family life and work. However, my children have now both gone to university, so I am thinking to myself that I need a hobby! Of course, when you don’t have a hobby what happens is that you work all the time. I am very privileged in that I really enjoy my job and I love being in touch with all that is going on in my lab!

Thumbs up (4 votes)
Loading...

Tags: , , , ,
Categories: Interview

In Development this week (Vol. 142, Issue 16)

Posted by , on 18 August 2015

Here are the highlights from the current issue of Development:

 

Probing gene expression dynamics in stem cells

New Figure 3The accurate control of gene expression is essential for cell differentiation during development but how do heterogeneous and fluctuating gene expression levels influence cell fate choices? Here (p. 2840), using a novel quantitative and high-content imaging platform, Jonathon Chubb and colleagues investigate how various cell- and population-based features are coupled to Nanog reporter expression in mouse embryonic stem cells (ESCs). They first show that cell cycle times are heterogeneous within ESCs but correlate with Nanog reporter expression; low expression levels are found in both long and short cell cycles but reporter expression tends to be highest in longer cycles. The transition to ground-state pluripotency (triggered by 2i treatment), they report, correlates with longer and more variable cell cycle times. Looking at lineage history, the researchers further reveal that all cells within a lineage are strongly related with regards to both cell cycle times and reporter expression. Modelling further suggests that some element of the cell environment plays a role in stabilising gene expression between generations. Finally, the researchers highlight a correlation between cell density and both cell cycle behaviour and reporter gene expression. Based on these and other findings, the authors propose that simple deterministic views of stem cell states need rethinking.

 

Fattening up neural development

DEV123539F2Fat family atypical cadherins are known to regulate planar cell polarity and growth control in Drosophila. In mammals, four Fat genes (Fat1 to Fat4) have been identified but relatively little is known about how these regulate mammalian embryogenesis. Here, Helen McNeill and co-workers identify a role for Fat proteins in regulating various aspects of brain development in mice (p. 2781). Using mutant mice, the researchers first identify a role for Fat1 in neural tube closure; Fat1mutants display cranial neural tube closure defects leading to exencephaly. They further show that the cortex of these mutant embryos exhibits elongated ventricles, linked to an increase in radial precursor cell proliferation. Accordingly, the knockdown of Fat1 by in utero electroporation in the developing cortex causes an increase in radial precursor cell proliferation and perturbs neuronal differentiation and migration. The researchers further show that Fat4 interacts genetically with Fat1 to control these processes. Finally, they reveal that Fat1 and Fat4 bind to distinct sets of actin regulators and apical junction proteins, respectively. Together, these findings lead the authors to propose a model in which Fat1-Fat4 dimer formation brings together diverse proteins at apical junctions to regulate both apical constriction and progenitor cell divisions in the neural tube.

 

Tissue regeneration: from Hippo to flies and fish

The Hippo pathway, best known for its role in growth control, has been implicated in tissue repair and regeneration in various contexts. In this issue, two papers provide insights into how Hippo signalling regulates tissue growth during regeneration.

Figure 1In the first report (p. 2740), Joy Meserve and Robert Duronio study the Drosophila eye to investigate the mechanisms that allow quiescent cells to re-enter the cell cycle and proliferate in response to tissue damage. Using an RNAi screen, they reveal that scalloped (sd), which encodes a transcriptional effector of the Hippo pathway, is required for compensatory proliferation following tissue damage. They demonstrate that Sd and its binding partner Yorkie (Yki) are required to induce Cyclin E expression and hence drive S-phase entry in regenerating eye discs. The researchers further show that Ajuba (Jub), an upstream regulator of Hippo signalling, is needed for cell cycle re-entry. Given the roles of Jub in sensing epithelial integrity, the authors propose that the apoptotic force induced by tissue damage in this context triggers Jub and Sd/Yki activation that, in turn, allows for compensatory proliferation and tissue repair.

DEV2752In a second paper, Antonio Jacinto and colleagues reveal a role for the Hippo pathway effector Yap in zebrafish fin regeneration (p. 2752). Fin regeneration involves three steps – wound healing, blastema formation and tissue outgrowth – and the researchers show that Yap activation (and hence nuclear localisation) is dynamic during these steps. Yap is nuclear during wound healing, remains nuclear during blastema formation, and then is cytoplasmic in regions distal to the wound but nuclear in proximal regions during outgrowth. They further show, by modulating Yap levels, that Yap regulates cell proliferation and the expression of key regeneration factors. The researchers also report that Yap localisation correlates with changes in cell density and cell morphology along the blastema proximal-distal axis. Finally, they observe similar gradients in α-catenin and F-actin localisation, suggesting a model in which a mechanotransduction process involving changes in cell morphology, junctional assembly and the cytoskeleton controls the activation of Yap to regulate tissue regeneration.

 

PLUS:

 

Caroline DeanAn interview with Caroline Dean

Caroline Dean is a plant biologist based at the John Innes Centre in Norwich, UK, who works on the epigenetic mechanisms that regulate vernalisation. We talked to Caroline about her career, her FEBS EMBO Women in Science Award, and her thoughts on the plant field. See the Spotlight article on p. 2725

 

The embryo reunited with its membranes in Göttingen

In this meeting review, Claudio Stern summarises the work and advances presented at the recent EMBO Workshop ‘Embryonic-Extraembryonic Interfaces’, which took place in Germany. See the Meeting Review on p. 2727

 

Primordial germ cells: the first cell lineage or the last cells standing?

In this Hypothesis article, Johnson and Alberio propose that the determinative mechanisms for PGC specification in most model systems evolved to promote speciation and evolvability, not to maintain the germ line. See the Hypothesis on p. 2730

DEV2730b

Thumbs up (No Ratings Yet)
Loading...

Categories: Research

On progressing your career and communicating your science- Advice from the SDB meeting

Posted by , on 17 August 2015

Last month I attended the SDB annual meeting in Utah, an excellent conference that featured great scientific talks and additional educative sessions covering outreach, inclusiveness and more. I tweeted extensively from the Node’s twitter account, but as many of the readers of the Node are not on twitter, I realised that you may have missed out on some of the great advice shared at the meeting. So here is the roundup of some the thoughts and recommendations shared at the conference!

 

On progressing your scientific career:

 

Brigid Hogan was awarded this year’s SDB Lifetime Achievement Award, and gave a great talk on her life and career so far, and the lessons she learnt along the way:

  • You have to take risks if you want to follow your passion and do something important.
  • Seek out people who will give you criticism, even if it is difficult. It will help you do better.
  • Share the resources (reagents and ideas) you have generated. It will help you know people and they will share their resources with you.
  • Be confident in your own results.
  • Find good role models, not just for how you do science but also on how to deal with important social issues.
  • Have your 2 minute elevator speech ready. You never know when it will come handy! (read our interview with Brigid for her account of how a well-timed 2 minute speech helped her establish the CSH course on mouse embryology).
  • Never go to a organisational/administrative meeting unprepared. Form your coalitions beforehand.
  • Trust your own scientific judgement and seek impartial advice when making a career move.
  • Interactions with clinicians can be very rewarding.
  • Keep embracing new technologies and apply them to your system. One of the best ways to keep up with what’s new is to attend meetings.
  • Publish, publish, publish- stories are never complete and others will find your data useful

 

Kathryn Tosney was the winner of the Viktor Hamburger Outstanding Educator Prize, and gave a varied talk that ranged from her work on growth cones to her recent iguana preservation project. During her career she has been involved in many aspects of mentoring, and here are some of her thoughts:

  • Descriptive has become a bad word in science, but it’s essential to frame your question. Looking is important.
  • Advice to postdocs- don’t assume you can take your project with you when you start your own lab. This will have to be negotiated with your PI.
  • Advice for new assistant professors (echoing Brigid’s thoughts)- write your papers as you go along, and publish early. Early publications help to establish that you are respected, independent and productive.
  • Good letters from prominent supporters are key for promotion.
  • Presenting a good poster is important to make connections. Write a good title that states the result and why is important
  • In science the workload is too high, the pay is too low, it can be frustrating… It can’t just be a job, must be a passion!

 

Japanese fans2
Biology uchiwa (japanese fan), spotted at the RIKEN CDB stand

 

 

On communicating your science

One of the additional sessions on the conference was the education symposium, where the do’s and don’ts of science communication (at many levels) were discussed. Chanda Jefferson is teacher who won this year’s South Caroline Biology Teacher of the Year award. She told the audience what teachers need from scientists:

  • Give your research a hook- something to remember. E.g. the title of Bonnie Bassler’s TED talk on quorum sensing is a great hook: ‘How do bacteria talk?’- this is something that gets the students interested!
  • Make research fun- what is the coolest, the grossest bit of your research? Turn it into a story.
  • Make your work relevant to students, generalise to something they can relate to.
  • Develop data-based activities: give your own data to the class to analyse, help teachers develop practical lab activities.

 

In the same session Karen Weintraub, a freelance journalist, talked about what journalists need from scientists when they are writing a story:

  • Speak English, not science. And don’t be condescending- journalists are not idiots, they just aren’t specialists in your field
  • Share your passion for the work- don’t assume it is obvious.
  • Put your work in a broader context. Don’t exaggerate your findings but don’t underplay them either.
  • Pretty images make your research easier to understand, and are more likely to get visibility.
  • Use metaphors and analogies.
  • It is good to have notes, but don’t just read what you wrote. A good interview is a conversation between the journalist and the scientist.
  • Sharing personal details and experiences may be uncomfortable, but helps the public connect and care about the research.
  • Journalists are just as intimidated by you as you are by them!
  • Journalists are under pressure and over-worked. They need your help to write the best story that they can!

 

What good advice (on this or other topics) was shared at recent meetings you have attended? Leave a comment here and share it with the rest of the community!

 

Sciart posters spotted at SDB
Sciart posters spotted at SDB

 

Thumbs up (1 votes)
Loading...

Tags: , ,
Categories: Discussion, Education