Presentation on theme: "Animal Development Drosophila axis formation Part 1: A-P patterning"— Presentation transcript:
1Animal Development Drosophila axis formation Part 1: A-P patterning Part I introduces Drosophila development, the life cycle, terminology and tissues. Oogenesis and early embryogenesis. The role of maternal and zygotic gene expression is discussed. There is a overview of the hierarchy of genes controlling anterior-posterior patterning and segmentation. This introduces the practical that follows in TT.The core part of this lecture is concerned with dorsal-ventral patterning, the different signals that establish asymmetry in the embryo and some of the mechanistic principles underlying these pathways. A recurring theme is how different signalling pathways may be recruited to different developmental processes both in Drosophila and in vertebrates.Synopsis: Review of Drosophila life cycle, terminology and tissues. Maternal and zygotic gene expression. Origin of the asymmetry and localised determinants in the egg. Subdivision and specification of the embryonic pattern. Transcriptional and translational regulation in embryogenesis. Where to study signal transduction pathways.
2Problem: starting point where all cells have the same developmental potential (because they have the same DNA)However, the end point is the production of nerve cells, muscle cells, epithelial cells etc. Therefore differentiation happens. Mechanism?
5Diagrams representing a group of mesenchymal cells that emit a signal (black dots) Diagrams representing a group of mesenchymal cells that emit a signal (black dots). The different shades of blue (in the mesenchyme) and green (in epithelia) depict different signal concentration thresholds (and thus possibly the induction of different mesenchymal types). (A) The mesenchymal cells are depicted by the black circle. Note that the spatial distribution of the signal at different concentrations is a linear extrapolation of the shape of the signal-emitting tissue. (B) The signal arises from a part (black) of a folded epithelium (green) and diffuses in the mesenchyme (blue) without being able to cross the epithelium. (C) Here, the invaginated epithelium encloses less space, which causes less signal dilution. As a result, larger amounts of epithelium receive high signal concentrations. The same number of dots are depicted in B and C. (D) In epithelia with more complex shapes, the mesenchymal areas are not linear extrapolations of the shape of the signal-emitting tissue or of the diffusion space. Note that the borders of these areas have different curvatures at different distances from the source as a result of the different shapes of the diffusion space. (E,F) In E, diffusion is occurring before the invagination, whereas in F it is occuring afterwards. Morphostatic mechanisms involving signalling and invagination produce the three spatial distributions of mesenchymal types depicted in blue (E). Morphodynamic mechanisms can produce the shapes in E and F and others at intermediate stages of the invagination. Thus, morphodynamic mechanisms can generate a larger diversity and disparity of spatial distributions.Salazar-Ciudad I Development 2010;137:
6In this lecture: The origin of Anterior-Posterior Axis Mutant screens to isolate segmentation genesGenetic analysis of early acting determinantsImportant roles of post-transcriptional regulation and mRNA/protein localisationMethods of dissecting enhancersDosage-dependent activation of zygotic genesHierarchical organisation of segmentation genes
81 * egg: generate the system * larva: eat and grow Developmental biology:Drosophila segmentation and repeated units* egg: generate the system* larva: eat and grow* pupa: structures inlarvae grow out to formadult fly: metamorphosis(Drosophila is aholometabolous insect)1
12The early embryo is a syncitium The unusual feature of the Drosophila early embryo is that the first 13 mitoses are nuclear divisions without concomitant cytoplasmic division, making the embryo a syncitium-a multinucleated cell. After division 9, the plasma membrane of the oocyte evaginates at the posterior pole to surround each nucleus thus creating the pole cells, which will form the fly’s germ line.
13Segments in embryos are maintained throughout development
14Forming complex pattern: establishing positional information
15The Hunt for Mutants30,000 independently-derived mutants in genes required for survival.8,000 mutants define genes required for embryonic survival (these became the focus the study).750 mutants have specific effects on A/P or D/V patterning.150 genes with specific effects on A/P or D/V patterning identified by the 750 mutants (average of ~ 5 alleles per gene).
16A Detour Into Embryonic Anatomy – Denticle Bands Denticle bands on a 1st instar larva.Denticle bands are hair-like projections on the ventral cuticle of an embryo.Denticle bands provide an easily visualized marker of embryonic/larval pattern.
18Maternal effect genesPhenotype of the embryo is determined by the genotype of the mother.The polarity and spatial coordinates of the embryo are initially set by the products of these genes (therefore, sometimes called “coordinate genes”).The gene products, either mRNA transcripts, proteins, or cell surface ligands are contributed by the nurse cells or follicle cells as the egg is constructed.The dorsal-ventral axis (1 gene-system, 12 genes) and anterior-posterior axis (3 gene-systems; anterior, 4 genes, posterior, 11 genes, and terminal, 6 genes) determined by maternal effect genes.Originally isolated as homozygous mutant, adult females that lay normal looking eggs that do not develop at all, regardless of the genetic contribution of the male.
19Four Independent Genetic Regulatory Systems Specify the Anteroposterior and Dorsoventral Axes
20Maternal effect genes All four systems share several properties: (i) the product of (at least) one gene is localized in a specific region of the egg,(ii) this spatial information results (directly or indirectly) in an asymmetrical distribution of a transcription factor,(iii) the transcription factor is distributed in a concentration gradient that defines the limits of expression of one or more zygotic target genes, such as segmentation genes.
21Bicoid mutant embryos lack head and thorax structures bicoid/bicoidmother+/+mother
22The Importance of RNA localisation Essential for many fundamental processes:Cell polarityDevelopmental patterningNeural developmentLearning and memoryHamilton et al 2012, Biophysics for the life sciences Chapter 11
23Establishment of AP axis in oogenesis and bicoid localisation by Gurken signalling. In early stage egg chambers MTOC is in the oocyte, and gurken mRNA is localised at posterior.Translation and limited diffusion means signal sent to overlying posterior follicle cells (received via torpedo receptor).A signal is sent back which activates protein kinase A in the eggoocyte cytoskeleton is re-organised and directs the localisation of bicoid and oskar, defining the A-P axis.
24EGF signalling between the oocyte nucleus and follicle cells
31Effect of replacement of the 3’ UTR of the nos mRNA with the 3’ UTR of bcd mRNA The nos-bcd transgene is able to localise at the anterior pole and as a consequence NOS protein will inhibit translation of the hb and bcd mRNAs.
32The Bcd gradientmRNA (in situ)Protein (Ab staining)
33Concentration gradients of BCD and HB-M establish A-P axis Positional information along the A-P axis of the syncitial embryo is initially established through the creation of concentration gradients of two transcription factors: Bicoid (BCD) and Hunchback (HB-M). These are products of two maternal effect genes their mRNAs provided by the mother and stored in the embryo until translation initiates. These factors interact to generate different patterns of gene expression along the axis.
34Bicoid is an Anterior Morphogen Note that bicoid (and other maternal effect gene products) diffuse in the shared cytoplasm of the syncytial blastoderm.This is a unique feature of insect embryogenesis.
36Thresholds can turn gradients into sharp boundaries Bicoid protein required for early activation of zygotic hunchback.Bicoid contains homeoboxMutations in homeobox results in failure of Bicoid protein to interact with hunchback target sequences.
37bicoid protein gradient gradient is interpreted at least at four different levels (thresholds).
38bicoid as a repressor of posterior fates Bicoid binds the 3’ UTR of caudal mRNA and suppresses translation.Caudal protein enters the nuclei at the posterior end of the syncytial blastoderm and helps specify posterior fatesCaudal protein
39At the Posterior: nanos localisation by Gurken signalling oocyte cytoskeleton is re-organised and directs the localisation of bicoid and oskar, defining the A-P axis.oskar mRNA binds Kinesin I and Staufen proteins.Kinesin I localises oskar mRNA to posteriorStaufen allows translation of oskar mRNAOskar protein binds nanos
40Effect of posterior group genes on hunchback. primary gene is nanos.nanos mRNA is tightly localised to the posterior pole of the egg.
41Effect of posterior group genes on hunchback. The role of nanos is to disable hb maternal mRNA at the posterior end of the egg.
42Four Independent Genetic Regulatory Systems Specify the Anteroposterior and Dorsoventral Axes
45Segmentation patternObvious segmentation begins to develop by germ band extension stage.The embryonic segmentation pattern has direct analogs to the final segments of the adult.Segmentation pattern can be thought of as classical segments or midsegment-to-midsegment intervals called parasegments.Some early embryonic segments become incorporated into the complex structures of the head and mouth.
46SUMMARYNurse cells surrounding the oocyte in the ovarian follicle provide it with large amounts of mRNAs and proteins, some of which become localised in particular sites. The oocyte produces a local signal, which induces follicle cells at one end to become posterior follicle cells. The posterior follicle cells cause a re-organisation of the oocyte cytoskeleton that localises bicoid and hunchback mRNA to the anterior end and other mRNAs such as oskar and nanos to the posterior end of the oocyte. Following fertilisation, development starts and these mRNAs are translated. Subsequently, gradients of the BCD and HB proteins define the anterior nuclei-the embryo is still a syncytial blastoderm, while inhibition of translation of their mRNAs by Nanos define the posterior cells. Nuclei in between receive a variable amount of BCD and HB resulting in differential activation or repression of target genes and finally in different developmental cell fates.