Fgfr1a, fgfr1b, and fgfr2 function redundantly to regulate pectoral fin development. fgfr1a, fgfr1b, and fgfr2 function redundantly to regulate pectoral.

Slides:



Advertisements
Similar presentations
Sequence and expression of Xenopus EAF2.
Advertisements

Zebrafish homolog of the leukemia gene CBFB: its expression during embryogenesis and its relationship to scland gata-1 in hematopoiesis by Trevor Blake,
Volume 21, Issue 10, Pages (October 2014)
STAT5 acts as a repressor to regulate early embryonic erythropoiesis
Feng Liu, Maggie Walmsley, Adam Rodaway, Roger Patient  Current Biology 
Clarissa A. Henry, Sharon L. Amacher  Developmental Cell 
Volume 17, Issue 6, Pages (November 2016)
by Alex Bukrinsky, Kevin J. P
Katherine Joubin, Claudio D Stern  Cell 
Karen Lunde, Heinz-Georg Belting, Wolfgang Driever  Current Biology 
Eliminating Zebrafish Pbx Proteins Reveals a Hindbrain Ground State
Volume 35, Issue 2, Pages (July 2002)
Smoothened Mutants Reveal Redundant Roles for Shh and Ihh Signaling Including Regulation of L/R Asymmetry by the Mouse Node  Xiaoyan M. Zhang, Miguel.
Hyunsook Lee, David Kimelman  Developmental Cell 
Volume 19, Issue 2, Pages (August 2010)
Volume 18, Issue 3, Pages (March 2010)
Direct fusion lines allow fluorescent visualization of plasmatocyte nuclei, the cytoplasm, or the cytoskeleton in embryos from stage (St) 8 onwards. Direct.
nrde-3-dependent silencing of endogenous RNAi targets and transgenes.
Vagus Motor Neuron Topographic Map Determined by Parallel Mechanisms of hox5 Expression and Time of Axon Initiation  Gabrielle R. Barsh, Adam J. Isabella,
Activin-βA Signaling Is Required for Zebrafish Fin Regeneration
Genome-wide expression screen identifies novel hypoxia-regulated genes
Volume 19, Issue 19, Pages (October 2009)
Volume 8, Issue 4, Pages (April 2005)
Volume 8, Issue 6, Pages (September 2014)
Volume 7, Issue 1, Pages (July 2004)
Volume 44, Issue 2, Pages e5 (January 2018)
Molecular Targets of Vertebrate Segmentation
Volume 13, Issue 9, Pages (December 2015)
Vertebrate Segmentation: From Cyclic Gene Networks to Scoliosis
Volume 1, Issue 1, Pages (July 2001)
Volume 3, Issue 1, Pages 1-7 (January 2013)
Eph Family Transmembrane Ligands Can Mediate Repulsive Guidance of Trunk Neural Crest Migration and Motor Axon Outgrowth  Hai U. Wang, David J. Anderson 
Sonic hedgehog and vascular endothelial growth factor Act Upstream of the Notch Pathway during Arterial Endothelial Differentiation  Nathan D. Lawson,
The BMP Signaling Gradient Patterns Dorsoventral Tissues in a Temporally Progressive Manner along the Anteroposterior Axis  Jennifer A. Tucker, Keith.
Volume 16, Issue 5, Pages (March 2006)
Volume 19, Issue 12, Pages (June 2009)
A. A. The two independent mutations identified in the structural gene of pqn-82 are shown above the gene. The genomic coordinates for the altered base.
Volume 18, Issue 4, Pages (April 2010)
Whole‐mount in situ hybridization analysis of marker genes in wild‐type embryos and chokh mutants. Whole‐mount in situ hybridization analysis of marker.
Brian A Hyatt, H.Joseph Yost  Cell 
Volume 24, Issue 3, Pages (November 1999)
Di Jiang, Edwin M. Munro, William C. Smith  Current Biology 
Volume 94, Issue 3, Pages (August 1998)
Volume 149, Issue 2, Pages (April 2012)
Distinct mechanisms regulate slow-muscle development
FGF Signaling Controls Somite Boundary Position and Regulates Segmentation Clock Control of Spatiotemporal Hox Gene Activation  Julien Dubrulle, Michael.
Gfi1aa/1b do not mediate Npas4l/Cloche suppression in primitive red blood cells. Gfi1aa/1b do not mediate Npas4l/Cloche suppression in primitive red blood.
Norihito Kishimoto, Ying Cao, Alice Park, Zhaoxia Sun 
Pharyngeal arch patterning in the absence of neural crest
Gfi1aa suppresses the endothelial gene expression program in primitive erythroblasts developing from the posterior lateral mesoderm. Gfi1aa suppresses.
Defining the node-streak border, caudal lateral epiblast and chordo-neural hinge. Defining the node-streak border, caudal lateral epiblast and chordo-neural.
Cerebellar midline fusion and variations in the expression of roof plate markers at the MHB junction. Cerebellar midline fusion and variations in the expression.
P53 is responsible for the induction of apoptosis, developmental malformations and mortality of G1 and G2tert mutant zebrafish. p53 is responsible for.
Epidermal aggregation in clint1 mutants and interaction with lgl2.
Leukocyte infiltration of epidermis and phagocytosis of debris in clint1 mutants. Leukocyte infiltration of epidermis and phagocytosis of debris in clint1.
Loss of chw-1 but not crp-1 attenuates the defects in the VD/DD motor neurons driven by activated SAX-3. Loss of chw-1 but not crp-1 attenuates the defects.
prdm1a is co-expressed with foxd3 and tfap2a at the NPB
Reb does not play a significant role in regulating TGF-β signaling
Cyclopamine treatment blocks Hh signalling in Xenopus.
Properties of cBAF-overexpressing cells.
Reporter gene expression in transgenic zebrafish embryos recapitulates expression of wt1 paralogs. Reporter gene expression in transgenic zebrafish embryos.
Cell-autonomous migration of gata5/smarcd3b-expressing cells to the heart. Cell-autonomous migration of gata5/smarcd3b-expressing cells to the heart. (A-E)
Zebrafish as a Model Organism for the Identification and Characterization of Drugs and Genes Affecting p53 Signaling  Ulrike Langheinrich, Elisabeth Hennen,
The zebrafish swdp75fm and swdp82mf mutations cause exocrine pancreatic hypoplasia and reduced skin pigmentation. The zebrafish swdp75fm and swdp82mf mutations.
A Bmp/Admp Regulatory Circuit Controls Maintenance and Regeneration of Dorsal- Ventral Polarity in Planarians  Michael A. Gaviño, Peter W. Reddien  Current.
A tph2 promoter fragment labels DR serotonergic neurons.
Mutations in the zebrafish hmgcs1 gene reveal a novel function for isoprenoids during red blood cell development by Jose A. Hernandez, Victoria L. Castro,
Volume 23, Issue 11, Pages (June 2018)
Zhen Zhang, Jamie M. Verheyden, John A. Hassell, Xin Sun 
Volume 18, Issue 6, Pages (June 2010)
Presentation transcript:

fgfr1a, fgfr1b, and fgfr2 function redundantly to regulate pectoral fin development. fgfr1a, fgfr1b, and fgfr2 function redundantly to regulate pectoral fin development. (A) Model of pectoral fin bud development during pectoral fin bud Induction (top) and Outgrowth (bottom). Underlines denote genes assayed in (C–H). Arrows denote an epistatic (but not direct) link between molecules. Asterisk signifies that Fgf8 has not yet been shown to play this role in zebrafish, but is hypothesized from forelimb work in chick and mouse. (B) Stacked column chart depicting the average number of pectoral fins per animal at 5 dpf, according to genotype. Sample size for each genotype is listed at the top of each bar. Representative images of larvae with 2, 1, or 0 pectoral fins to the right: dorsal views, anterior to the left, with arrowheads denoting pectoral fins where present. (C–H) Fin bud marker analysis of fgfr double and triple mutant embryos at the 18-somite stage (tbx5a, C), 24 hpf (fgf24, D; fgf10a, E), and 44 hpf (fgf24, F; fgf8a, G; dlx2a, H). Whole mount in situ hybridization was performed, embryos were scored for expression, and genotypes were determined post hoc. In each panel, the percentage of embryos expressing particular levels of each marker gene is represented in a stacked column chart on the left, and representative images of those expression levels are shown for each marker to the right (dorsal views, anterior up; developing fin buds are seen as two spots on either side of the embryo, denoted by arrowheads). Bars: in (B), 200 μm; in (C), 50 μm for (C–H). Dena M. Leerberg et al. Genetics 2019;212:1301-1319 Copyright © 2019 by the Genetics Society of America