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Post-translational regulation of epidermal morphogenesis

Posted by , on 17 November 2015

Closing Date: 15 March 2021

My laboratory is looking for PhD students to study the roles of SUMO proteases in embryogenesis. Our goal is to reveal the main targets of these enzymes during epidermal morphogenesis in C. elegans and their mode of regulation.
Highly motivated candidates with a Master degree in biological sciences and an interest in cell biology, genetics, and/or developmental biology are encouraged to apply. Successful applicants must be fluent in English (both written and spoken) and be able to work independently as well as part of an international team. Preference will be given to candidates familiar with advanced microscopy and molecular biology techniques. Interested candidates should email their CV as well as a brief paragraph describing their research interests and expertise, to Dr. Broday.

 

Reference

http://www.cell.com/developmental-cell/abstract/S1534-5807(15)00553-5

 

 

Limor Broday, Ph.D.

Dep. of Cell and Developmental Biology

Sackler School of Medicine Rm417

Tel Aviv University

Tel Aviv 69978

Israel

 

Office: 972 3 640-6653

Lab:    972 3 640-8225

Fax:    972 3 640-7432

email: broday [at]post.tau.ac.il

 

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Developing a new look

Posted by , on 17 November 2015

This editorial first appeared in Development, and it was authored by Olivier Pourquié, Katherine Brown and Claire Moulton.

 

As you might have noticed, Development has been looking a little different recently, with a new website and a new masthead for the journal (see Box 1 for elements of our new branding). These changes mark the culmination of a series of projects we’ve been working on over the past year at The Company of Biologists, aimed at improving the experience for our readers and at promoting the activities and values of the Company. Our website (and those of our sister journals) has undergone more than just a visual makeover – we have de-cluttered our pages and improved navigability, and the new open source platform will allow us to implement additional functionalities in the future. The consistent design, applied across all our journals, the Company’s own website (http://www.biologists.com/) and that of our community blog the Node (https://thenode.biologists.com) aims to provide clearer brand recognition and a better user experience – we hope you like it!

 

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Box 1. A new look for the Company and its journals

The Company of Biologists logo:

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Development’s new masthead:

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Since you are reading this editorial, you are probably at least reasonably familiar with the journal, and many of you will know something about The Company of Biologists, the publisher behind it. But we’d like to take this opportunity to let you know a bit more about who we are, what we do and how we help the scientific community. The Company of Biologists is a not-for-profit organisation dedicated to supporting and inspiring the biological community. At the heart of the Company are our five journals – Development, Journal of Cell Science, Journal of Experimental Biology, Disease Models & Mechanisms and Biology Open – and our primary mission is to publish influential and innovative science, providing a valuable forum for sharing scientific knowledge. Our journals cover a broad range of the life sciences, from comparative physiology to drug discovery, but they all aim to provide an important platform for their respective communities: to disseminate research to the community in an accessible manner and to make the publication process as pain-free as possible (for some of the benefits of publishing in Development, see Box 2). For example, at Development we recently changed the way we ask our reviewers to assess papers (Pourquié and Brown, 2015), with the aim of easing the path to publication while still maintaining our high standards. We hope this is making a difference for authors (we welcome your feedback), and we will continue to review and improve our processes.

 

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Box 2. Key information about the policies, processes and benefits of publishing in Development

  • Free to publish: no page or colour charges.

  • Editorial decisions made by expert Academic Editors who know and understand your field.

  • Fast publication, online and in print.

  • Avoidance of multiple rounds of review wherever possible; strong commitment to publishing invited revisions.

  • Scoop protection: we won’t reject your manuscript on the grounds that a competing paper has come out after yours was submitted.

  • Author-pays Open Access publication option available.

  • All articles freely available online six months after publication; online archive dating back to 1953.

  • Open attitude to sharing research results and data on pre-print servers and data repositories.

  • Informative and provocative Review and Hypothesis-type articles written by leaders in the field.

  • All articles copyedited by experienced scientific editors.

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Another way we have tried to help in reducing ‘the pain to publish’ is through our newest journal, Biology Open (BiO; http://bio.biologists.org), which we launched as a response to community feedback. As a fully Open Access journal, BiO supports the rapid publication of scientifically sound research across the biological sciences, without making judgement on the ‘impact’ of the work. Importantly, papers rejected from Development can be transferred to BiO, where their editors (including developmental biologists Anna-Katerina Hadjantonakis, Yishi Jin and Jenny Nichols) can use the Development referee reports to make swift decisions on the potential suitability of these papers for BiO, thus streamlining the process and hopefully allowing authors to get their research results out to the community more quickly (see Box 3 for recent BiO papers of interest to the developmental biology community). While we know that developmental biologists have a wide choice of specialist journals to which they can submit, we believe that BiO provides a valuable alternative – particularly in cases where the prime objective is to get a paper published with minimum hassle.

 

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Although our journals are our most important output, the Company is much more than just a publisher. As a UK-registered charity, we believe that the profits from publishing the hard work of biologists should support scientific discovery and help develop future scientists. Each year, we provide significant financial support to the community through our various charitable programmes, overseen by our dedicated Board of Directors – distinguished practising scientists who give up their time free of charge to help oversee the Company’s activities.

So where does this money go? We run a very active Meeting Grants programme (http://www.biologists.com/grants/), providing support to help defray the significant costs of putting on a conference. We also believe in supporting young scientists to learn new techniques, make new scientific connections and experience different scientific cultures: our Travelling Fellowships provide funding for researchers to make collaborative visits to other labs (http://www.biologists.com/travelling-fellowships/; see also Box 4). We also provide large grants to several societies, including the British Society of Developmental Biology (BSDB; http://bsdb.org/). Part of this money is used by the society to help run its annual meeting, while the rest is dedicated to a travel grants programme, to which BSDB members of any nationality can apply for funding to help pay for attendance at conferences across the globe (see http://bsdb.org/membership/meeting-grants/company-of-biologists/).

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Box 4. A Development Travelling Fellowship story: The benefits of global collaboration

Mirana Ramialison has been able set up her own lab at the Australian Regenerative Medicine Institute in Melbourne – thanks in part to Development.

Mirana had been a bioinformatician post-doc in the laboratory of Professor Richard Harvey, at the Victor Chang Cardiac Research Institute in Sydney. Her project consisted of deciphering the regulatory network that controls heart development and how this network might be perturbed in disease conditions, such as congenital heart disease. This involved genome-wide information obtained using a mouse cell line (HL-1 cells). Mirana wanted to further investigate how this cardiac gene regulatory network changed (or not) during evolution. This new project required genome-wide information on cardiac-specific cells from different organisms, including zebrafish. The laboratory of Dr Eileen Furlong at EMBL Heidelberg in Germany had published a new method, BiTS-ChIP-seq (Bonn et al., 2012), that allows researchers to obtain genome-wide information from tissue-specific cell types in vivo. Mirana saw that using this method in the developing zebrafish, in a transgenic line that specifically labels heart nuclei, would help gain insight into the nature of this gene regulatory network in vivo.

The published protocol was detailed and complex and included many techniques that Mirana has never performed before. The quickest way to get these experiments going was to get ‘hands-on’ experience of this protocol – but Australia is far from Heidelberg. A Travelling Fellowship from The Company of Biologists made the visit possible, providing Mirana with the hands-on experience to learn the protocol and its ‘tricks’, saving months of trials to get it right.

The Travelling Fellowship also had repercussions beyond research; Mirana was in the process of looking for an independent position and finding grants to fund it. The collaboration with Dr Furlong’s laboratory on the BiTS-ChIP-seq experiments gave the evidence of collaboration that the Australian Research Council needed. Not only did the Travelling Fellowship help save time on experiments, it strengthened connections around the world and helped Mirana to start her own laboratory.

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More recently, we started hosting our own series of Workshops (http://www.biologists.com/workshops/), bringing together small groups of leading experts and young scientists (who can apply to attend with no registration fees) from a diverse range of scientific backgrounds for the cross-fertilisation of interdisciplinary ideas. The unique format of these Workshops has proved a huge success, with overwhelmingly positive feedback from organisers and participants alike, and we welcome proposals for future events. Finally, we are now organising Meetings on topics of particular interest to the journals (http://www.biologists.com/meetings/). The first of these focussed on the emerging field of human development (for a review of the Meeting, seeMedvinsky and Livesey, 2015) and was such a success that we will be running a second Meeting on the same topic in 2016 (see http://www.biologists.com/meetings/from-stem-cells-to-human-development-2016/) – we hope some of you will be able to join us!

We hope this brief overview of the activities of the Company has given you some idea of how we strive to help the scientific community. For further information, we encourage you to browse our website (http://www.biologists.com/) to see how you – whether you’re starting out in your career or you’re an established group leader – can benefit from what we do. Our ethos, ‘Supporting biologists, inspiring biology’, influences all that we do. We hope that by publishing in, reviewing for and reading Development you will continue to support the journal and the Company and, through us, the community at large.

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Categories: News

In Development this week (Vol. 142, Issue 22)

Posted by , on 17 November 2015

Here are the highlights from the current issue of Development:

 

Nodal: sustaining Shh expression

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Underlying the developing vertebrate forebrain is the prechordal mesoderm, which secretes sonic hedgehog (Shh) at a precise developmental time. The tight temporal regulation of this morphogen is crucial for the specification of several ventral cell types in the forebrain. However, little is known about the signals that limit Shh expression temporally. Nodal is expressed in the prechordal mesoderm and had previously been suggested to interact with Shh during ventral forebrain development. Now, using the chick embryo, Marysia Placzek and colleagues (p. 3821) show that Shh expression in the prechordal mesoderm is regulated by proNodal, the precursor of Nodal. Surprisingly, proNodal maintains Shh expression by a non-canonical route: binding to and activating FGFR3. Through this route, proNodal antagonises BMP7 and pSmad1/5/8, which suppresses Shh expression. Together with previous findings, this study suggests that whereas Nodal operates through canonical signalling to induce prechordal mesoderm, it acts via a non-canonical route involving FGFR3 to control the expression of Shh in the prechordal mesoderm.

 

Hh puts the pressure on boundaries

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The Drosophila wing originates as an imaginal disc, which is divided into anterior and posterior domains separated by a straight antero-posterior (AP) boundary. This barrier is characterised by an actomyosin cable and increased mechanical tension at cell junctions, termed cell bond tension. Engrailed and Invected, expressed in the posterior compartment, maintain the straight morphology of the AP boundary both through the induction of the morphogen Hedgehog (Hh) and via an Hh-independent mechanism. How do such signalling pathways regulate cell bond tension at the AP boundary? In this study (p. 3845), Christian Dahmann and co-workers show that the difference in Hh activity between the two compartments drives the local increase in cell bond tension along the AP boundary and is required to bias cell intercalations to maintain its straight shape. Furthermore, increased mechanical tension is generated autonomously at the boundary and does not depend on the actomyosin cable or the Hh-independent mechanism that contributes to the preservation of the AP boundary shape. By linking the molecular players and mechanical determinants, this study sheds light on the mechanisms governing the physical separation of adjacent cell populations destined to different cell fates.

 

Deciphering genome imprinting

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Following fertilisation, a genome-wide demethylation wave reprogrammes the genome. However, in mammals, certain loci can remain methylated specifically on the maternal or paternal chromosome, i.e. imprinted, in somatic cells. It was previously shown in transgenic mice carrying a fragment of the H19imprinting control region (ICR) that the paternally inherited H19 ICR does not need to be methylated in the germline to be imprinted, pointing at the existence of an unknown epigenetic mark inducing post-fertilisation methylation of that locus. Now, using the same H19 ICR transgenic line, Keiji Tanimoto and co-workers (p. 3833) show that H19 ICR imprinting is achieved through maternally inherited DNMT3A- and DNMT3L-mediated de novo methylation. This process is also at play at the endogenous H19 locus. Further, the authors identify the sequences responsible for the post-fertilisation methylation of the transgenic H19 ICR and show that their removal from the endogenous locus leads to partial H19 ICR demethylation and delayed embryonic growth in the offspring that inherited the mutation. These results provide a mechanistic understanding of the contribution of de novo methylation to genomic imprinting in the absence of germline methylation, though the nature of the putative epigenetic mark that directs this methylation has yet to be discovered.

 

A genome-wide view on cell differentiation

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The acquisition of specific cell fates in the early embryo is driven by changes in gene regulatory networks that induce differential expression of effector genes to ultimately instruct a specific cell fate. The activation of such effector genes has been well characterised in time for individual genes, but to a much lesser extent in space. Here (p. 3892), Julius Barsi, Eric Davidson and colleagues performed a quantitative transcriptomic analysis of effector gene activation on a genome-wide scale in six cell populations isolated from different regions of pregastrular and early gastrula sea urchin embryos. With this approach, the authors identify a set of effector gene transcripts shared by the different cell populations. Surprisingly, this shared set of genes is not as large as previously thought. Indeed, the authors show that spatially distinct populations in the early embryo actually display profound differences in effector gene expression long before morphological differences in cell types can be distinguished. This study sheds light on the mechanistic essence of embryonic differentiation and provides a large-scale transcriptomic dataset, a rich resource for the developmental community.

 

Distilling principles of tubulogenesis

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In the developing Drosophila trachea, the maturation of tracheal terminal cells involves the generation of gas-filled tubular branches. However, the mechanism underlying subcellular lumen formation in these cells remains unknown. By adapting high pressure freezing and freeze substitution techniques toDrosophila larvae and performing transmission electron microscopy, Mark Metzstein and Linda Nikolova (p. 3964) show that, contrary to previous belief, lumen formation is not achieved by the direct fusion of cytoplasmic vesicles. Instead, the authors find that it requires a previously undescribed intermediary membrane-lined multivesicular compartment. In this compartment, vesicles assemble and then fuse into a nascent lumen. By further adapting their ultrastructural imaging technique to preserve the fluorescence of protein reporters and performing correlative light and electron microscopy, the authors show that the resolution of the multivesicular intermediate into a mature lumen requires Rabconnectin-3-mediated acidification of the compartment by the V-ATPase proton pump. The tools developed in this study to analyse tubulogenesis in the trachea and the insights provided on the mechanisms underlying this process are likely to contribute to the understanding of lumen formation in other organs.

 

Hox6: establishing a dialogue during pancreas development

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The development of the pancreas, a secretory organ that expands from the endoderm into the surrounding mesoderm-derived mesenchyme, requires a dialogue between its endodermal and mesodermal components. How do these two compartments communicate? To understand the molecular basis of this cellular cross-talk, Deneen Wellik and colleagues (p. 3859) have analysed pancreas organogenesis in mouse, finding that Hox6 genes, a group of patterning genes expressed in the pancreas mesoderm but not in the endoderm, play a crucial role in this process. Indeed, the genetic loss of all Hox6 paralogues results in mild defects in branching and in exocrine differentiation, and a drastic loss of mature endocrine cells. Mechanistically, the authors show that Hox6 depletion results in decreased expression of mesenchymal Wnt5a, a morphogen crucial for pancreas development. This then leads to the loss of the expression of two Wnt inhibitors, Sfrp3 and Dkk1, in endocrine progenitors. Hence, as repression of Wnt signalling in developing endocrine cells is crucial for their differentiation, this study highlights that regional mesodermal patterning cues are essential for the establishment of the mesenchymal/endodermal crosstalk necessary for pancreatic development.

 

PLUS:

 

Developing a new look

Embedded ImageAs you might have noticed, Development has been looking a little different recently, with a new website and a new masthead for the journal. These changes mark the culmination of a series of projects we’ve been working on over the past year at The Company of Biologists. Read more about these changes in the Editorial on p. 3803

 

Glia in mammalian development and disease

Figure1The past few decades have witnessed a flood of studies that detail novel functions for glia in nervous system development, plasticity and disease. Here, Bradley Zuchero and Ben Barres review the origins of glia and discuss their diverse roles during development, in the adult nervous system and in the context of disease. See the Development at a Glance article on p. 3805

 

Next generation limb development and evolution: old questions, new perspectives

Fig. 1.In recent years, systems biology approaches have aided our understanding of the molecular control of limb organogenesis, by incorporating next generation ‘omics’ approaches, analyses of chromatin architecture, enhancer-promoter interactions and gene network simulations based on quantitative datasets into experimental analyses. Here Aimee Zuniga reviews the insights these studies have given into the gene regulatory networks that govern limb development, the fin-to-limb transition and digit reductions during evolution. See the Review on p. 3810

 

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Categories: Research

PhD and postdoc positions at IST Austria

Posted by , on 16 November 2015

Closing Date: 15 March 2021

PhD and postdoc positions are currently available in the lab of Anna Kicheva at IST Austria, working on vertebrate neural tube development. Candidates with background in developmental, cell or molecular biology or at the interface between biophysics and biology are encouraged to apply.

During development, tissues increase considerably in size at the same time as cell type diversity is generated. How these processes are coordinated to achieve the correct size and morphological proportions of organs is a fundamental question in developmental biology. While much is known about how extrinsic signals, called morphogens, control the specification of cell identities, the mechanisms of tissue growth control are not well understood. Our aim is to gain a quantitative understanding of how neural progenitor cells in the developing spinal cord interpret morphogen signalling to regulate their progression through the cell cycle. We will also investigate how tissue growth affects the formation of morphogen gradients and pattern specification. The work will involve live imaging of mouse and chick embryos in both ex vivo and in vivo assays, as well as collaborating with theorists to analyse and interpret data.

IST Austria is a young international research institute close to Vienna, with a strong focus on interdisciplinary research and access to excellent facilities. PhD student candidates are required to apply through the IST graduate school, deadline January 8, 2016. To apply for a postdoc position, please email me at anna.kicheva@ist.ac.at with your CV, motivation letter and contact information for 2-3 references.

For more information: Kicheva lab IST, anna.kicheva@ist.ac.at

 

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Categories: Jobs

Post-doctoral Research Associate, UCL, in London

Posted by , on 13 November 2015

Closing Date: 15 March 2021

We are seeking to appoint a Post-doctoral Research Associate to undertake research on the molecular mechanisms of eye induction/development and in vitro eye construction from mammalian stem cells with Prof. Shin-ichi Ohnuma.

The work brings together a range of multi-disciplinary approaches including in vivo analysis of Xenopus eye development, in vitro stem cell biology, and molecular biology, in conjunction with a variety of imaging and data analytical approaches.

This project builds on the recent publication of the group: Luehders, K. et al, Development (2015) 142, 3351-3361.

Applicants should have a PhD and research experience in developmental biology. Previous experience in Xenopus development and/or stem cell biology is preferable. Applicants will be self-motivated, have the ability to plan and interpret experimental studies as well as have excellent communication skills and ability to write well.

The position is available for 36 months in the first instance.

The laboratory is well equipped and is part of UCL Institute of Ophthalmology. The Institute comprises about 40 research groups spanning a research area encompassing visual development, stem cell based study, and therapy of retinal diseases. UCL has active neuroscience, developmental biology, and stem cell research communities and the group has established collaborative links within the institute and UCL, as well as with national and international colleagues.

 

UCL Reference: 1514567

 

Applicants should apply online through UCL Job search webpage. Please input the number above, fill in your information and apply.

 

Informal inquiries may be addressed to s.ohnuma@ucl.ac.uk

 

Deadline of application: 6 th Dec 2015

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Categories: Jobs

4 Yr PhD Programme in Developmental Mechanisms

Posted by , on 13 November 2015

Closing Date: 15 March 2021

Applications are open for the Wellcome Trust funded four year PhD programme in Developmental Mechanisms at Cambridge. We are looking for talented, motivated graduates or final year undergraduates, and are keen to attract outstanding applicants in the biological sciences, who are committed to doing a PhD.  We are able to fund both EU and non-EU students.

Closing date:  8th January 2016

For more details about the application process and the programme please see the website:

http://devmech.pdn.cam.ac.uk/phd/

 

wtdm2015a4

 

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Categories: Jobs

New SDB Grants Initiatives

Posted by , on 10 November 2015

The Society for Developmental Biology has established several new small grant programs for the developmental biology community.

  • SDB Innovation Grant – to develop innovative tools and methods with the potential to have a broad impact on the developmental biology community – Deadlines: December 1 and May 31
  • SDB Emerging Models Grant – to develop techniques, approaches, community resources, collaborations, and new lines of research to study developmental mechanisms in non-traditional model systems – Deadlines: December 1 and May 31
  • SDB International Short Visit Grant – to help defray travel expenses for investigators from countries in which research in developmental biology is an emerging focus to visit host labs in the US or Canada for short periods of time to learn new techniques or approaches in developmental biology; this new program replaces the Latin American-Caribbean Short Visit Grant program – Deadlines: December 1 and May 31

The SDB Innovation and SDB Emerging Models grant programs require at least one applicant to be an SDB member.  The SDB International Short Visit Grant requires only that the PI of the host lab be an SDB member.

The existing Non-SDB Education Activities and Non-SDB Meetings grant programs will also be continued in 2016.

In order to meet the December 1 application deadline, renew or apply for SDB membership today.

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Post-doctoral researcher in heart development, Paris, France

Posted by , on 10 November 2015

Closing Date: 15 March 2021

In the Institut Imagine and Institut Pasteur, Paris France, the laboratory of Sigolène Meilhac is interested in the mechanism of heart morphogenesis. We focus on the regulation of cell behaviour by combining mouse genetics, quantitative analyses in 3D, cell and molecular biology.

Following from previous work in the team identifying a novel regulation of Hippo signalling in the mouse heart, we recruit a post-doctoral researcher to study this mechanism of heart growth. Such characterisation of a developmental pathway and how it can be re-activated in the more mature heart is relevant to heart repair.

After a PhD in biology, you have a solid experience in fundamental research. You work with rigour and creativity. You master cell cultures and molecular biology approaches and you have a strong interest in developmental biology.

The position, which is available at the beginning of 2016, can be funded initially. Applicants are encouraged to apply for fellowships.

Applications, including a covering letter, a curriculum vitae and contact details of three references should be sent to

sigolene.meilhac[at]pasteur.fr

https://research.pasteur.fr/en/team/heart-morphogenesis/

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A new look at the (microscopic) world- 350 years since Hooke’s landmark book

Posted by , on 9 November 2015

 

‘These pores, or cells, were not very deep, but consisted of a great many little Boxes … [they] were indeed the first microscopical pores I ever saw, and perhaps, that were ever seen’

 

Last month I was fortunate enough to attend the conference ‘Cell: from Robert Hooke to Cell Therapy- a 350 year journey’, which took place at the Royal Society in London. The focus of the meeting was new advances in cell therapies, particularly in the field of stem cells, and featured a stellar line-up of speakers. However, it was the first talk, given by historian Felicity Henderson, that really grabbed my attention. It highlighted an important anniversary that we are celebrating this year- the 350 years since Robert Hooke published his book Micrographia.

So why was Micrographia such an important book, and why should we, scientists, care about it? Well, it was quite simply the first illustrated book of microscopy. Hooke was not the first person to use a microscope. His Micrographia was published in 1665, but the microscope had already been around for a few years (since 1648 to be precise). However, Hooke was really the first person to make what you could see under the microscope accessible to anyone, even if you were not a scientist. So how did it fall onto him to write the first microscopy book?

 

Hooke R, IM002201

Microscopic view of a flea, Micrographia. Reproduced with permission by The Royal Society ©The Royal Society

 

Hooke was employed by the Royal Society, and in some ways he can be considered the first professional research scientist in the UK since, unlike other wealthy natural philosophers who had private means, Hooke was actually paid a salary by the Society. Within the Society he was responsible for a variety of activities, including preparing exciting practical experiments for the entertainment and interest of the other fellows.  The Royal Society was, in Hooke’s days, a newly founded institution, created in 1660 under the auspices of King Charles II. Charles II was very interested in science, and particularly enjoyed the images of microscopic creatures that Sir Christopher Wren (then the president of the Society) had given to him as a gift (and which he displayed alongside other works of art in his residence). In fact, Charles II liked them so much that he asked for more. In order to ‘win favour’ with their royal patron, the Society decided to publish a book (one of its first publications as an institution) showcasing the exciting microscopic science that was starting to be explored. Sir Cristopher Wren was too busy with other projects (designing St Paul’s Cathedral, for example?) so he asked Hooke to do it instead. The result of his efforts was a beautiful illustrated (and rather expensive) volume, worthy of a king! The project was a huge success with the public. Samuel Pepys, of the famous diary, said that it was so fascinating that he apparently stayed up all night reading it!

So why was Micrographia so popular? The most obvious feature is its beautiful (and numerous) illustrations. At a time when there were only a few microscopes (and no google), the book allowed the common man to see what was normally unseen. Hooke made all the illustrations himself. Before becoming a scientist he actually worked for some time in an artists’ workshop (although eventually left because the constant smell of paint made him sick!), so he had some formal training. However, the subjects of his illustrations were probably as important as their artistic qualities. One of the things I was most surprised to hear about in this talk was how sensitive Hooke was to what would grab the public’s interest. He may have been a 17th century scientist, but he had very 21st century ideas about what makes good science communication! He was aware that a way to make the work interesting to the public would be by focusing on everyday objects and critters. The very first image in the book, for example, features a needle, a printed full stop and a razor blade. One of the most popular images in the book (both then and today) is a big fold-out image of a flea, ‘the size of a cat’, and when Hooke wanted to show an image of a louse, he showed it holding on to a human hair (which is where most people at the time would come across it). Hook also understood the importance of using simple language that the public could follow. Micrographia was the book that coined the word ‘cell’. Hooke used it when describing a very thin slice of cork.  In this very thin slice you could see perforated holes. Instead of calling them ‘globules’ (a much more common word to describe microscopy structures at the time), Hooke called these holes ‘cells’, because they resembled honeycomb cells, something that the public was much more familiar with.

 

Picture 255

Microscopic view of cells in a sliver of cork, Micrographia. Reproduced with permission by The Royal Society ©The Royal Society

 

The way Hooke discussed the slices of cork is also a great example of something else that interested him. Explaining that the ability to see the microscopic world was not just a curiosity-it could help us understand how cells and organisms work. This was part of a new trend in the 17th century, a ‘new philosophy’, that focused on understanding how the world works in a mechanical way. Take the slice of cork. Hooke argued that this porous microscopic structure explained the properties of cork- how it was light and compressible. The beginnings of material science! Similar structures could also tell us about relatedness and natural history. Hooke noticed that charcoal and wood looked very similar under the microscope, displaying similar pores or ‘cells’, and this supported his theory that fossils are the remains of previous existing organisms. And, as if he was under the pressure of current funding trends, he hypothesised that some of these microscopic structures could be exploited or adapted into practical applications. He was intrigued, for example, by the sharp needles that he could observe in the leaves of stinging nettles. He could see that they were hollow and after some experimentation (by stinging himself repeatedly!) he concluded that they worked as syringes and hypothesised that similar structures might be used for medicinal purposes. Finally, he didn’t want the public to think that microscopy was some magic trick, and provided detailed instructions on how he prepared his specimens (in case you are wondering, ants move too much to look at them under the microscope, but dumping them in brandy for an hour does just the trick!).

Hooke was clearly a man ahead of his time, not only as a scientist but also as a communicator. Interestingly enough, and not unlike many of today’s communication efforts, his beautiful illustrations, useful metaphors and discussions of practical applications did not convince everyone. After all, what could be the use of spending your time looking at lice at such detail? It seems that the fight to persuade the public of the importance of science is several centuries long!

If you are interested in having a look at Micrographia yourself, head out to The Royal Society in London, where until the 17th of December you can see a small exhibition on the history of microscopy, including a first edition of this book. You can also find out more information about Hooke at Felicity’s blog Robert Hooke’s London.

 

Screen Shot 2015-11-09 at 12.13.29

A copy of Micrographia at The Royal Society.

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Engineer position in molecular biology and genetics

Posted by , on 9 November 2015

Closing Date: 15 March 2021

An engineer position in molecular biology and genetics is available starting in January 2016 at the Developmental Biology Institute of Marseille, France (http://www.ibdml.univ-mrs.fr/), in the groups of Pierre-François Lenne and Vincent Bertrand. Funding is provided by an ANR grant. The initial appointment will be made for 1 year, with a possible extension to up to 2 years. We are seeking a highly motivated candidate with experience in molecular biology and genetics. Experience in C. elegans would be desirable but not essential. The working language in the laboratory is English, so the candidate should have a good level in spoken and written English.

The main activities will be the implementation/optimization of CRISPR/Cas9 technologies to generate reporter lines in C. elegans and technical support to collaborative research projects, which require combinations of molecular biology, genetics and advanced imaging.

A letter of motivation, a CV and the names of two referees should be sent to Pierre-François Lenne (pierre-francois.lenneATuniv-amu.fr).

 

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Categories: Jobs