Expression of Abdominal-B homeoproteins in Drosophila embryos

Development ◽  
1990 ◽  
Vol 108 (2) ◽  
pp. 323-329 ◽  
Author(s):  
M. Delorenzi ◽  
M. Bienz
Keyword(s):  
Embryonic Development ◽  
Protein Expression ◽  
Molecular Analysis ◽  
Anterior Margin ◽  
M Protein ◽  
Control Mechanisms ◽  
Germ Layers ◽  
Separable Functions ◽  
Drosophila Embryos

The Abdominal-B (Abd-B) gene determines development of the posteriormost segments in Drosophila. Genetic and molecular analysis suggested that it consists of two genetically separable functions that are conferred by two related homeoproteins termed m and r. We have raised an antiserum against Abd-B protein to describe the patterns of Abd-B protein expression during embryonic development. The pattern of r protein expression, as deduced by analysis of Abd-B mutants, is restricted to ps14 and 15 in all germ layers and observes a parasegmental boundary at its anterior margin of expression. In contrast, the pattern of m protein expression is unusual as its level in the ectoderm increases from ps10 to ps13 in parasegmental steps. Its anterior margin of expression is highly dynamic shifting anteriorly across more than 3 parasegments during midembryonic development. Evidently, the control mechanisms of m and r protein expression are considerably different. Moreover, an antibody-positive Abd-B mutant suggests that these differ, in the case of m protein expression, to some extent in individual germ layers.

The localization and regulation of Antennapedia protein expression in Drosophila embryos

Cell ◽  
1986 ◽  
Vol 47 (1) ◽  
pp. 113-122 ◽  
Author(s):  
Sean B. Carroll ◽  
Robert A. Laymon ◽  
Michael A. McCutcheon ◽  
Peter D. Riley ◽  
Matthew P. Scott
Keyword(s):  
Protein Expression ◽  
Drosophila Embryos

scholarly journals Protein F1 and Streptococcus pyogenes Resistance to Phagocytosis

2007 ◽  
Vol 75 (6) ◽  
pp. 3188-3191 ◽  
Author(s):  
Kendra A. Hyland ◽  
Beinan Wang ◽  
P. Patrick Cleary
Keyword(s):  
Epithelial Cells ◽  
Protein Expression ◽  
Streptococcus Pyogenes ◽  
Binding Proteins ◽  
M Protein ◽  
Partial Inhibition ◽  
Fibronectin Binding ◽  
Negative Mutant

ABSTRACT Streptococcus pyogenes is a major cause of pharyngitis in humans and encodes several fibronectin-binding proteins. M protein and protein F1 (PrtF1/SfbI) are differentially regulated by CO2 and O2, respectively, and both mediate the invasion of epithelial cells. This study examined whether PrtF1/SfbI shares other properties with M protein. Expression of the PrtF1/SfbI protein by an M-negative mutant conferred resistance to phagocytosis and partial inhibition of C3 deposition on the S. pyogenes surface.

Mesoderm-inducing properties of INT-2 and kFGF: two oncogene-encoded growth factors related to FGF

Development ◽  
1989 ◽  
Vol 106 (1) ◽  
pp. 79-83 ◽  
Author(s):  
G.D. Paterno ◽  
L.L. Gillespie ◽  
M.S. Dixon ◽  
J.M. Slack ◽  
J.K. Heath
Keyword(s):  
Growth Factors ◽  
Embryonic Development ◽  
Xenopus Laevis ◽  
Dna Synthesis ◽  
Signalling Pathways ◽  
Control Mechanisms ◽  
Animal Pole ◽  
Receptor Signalling ◽  
Mammalian Embryogenesis ◽  
Mesoderm Formation

Many theories of neoplasia suggest that oncogenic transformations result from aberrations in the control mechanisms which normally regulate growth and differentiation during embryonic development. It has recently become clear that many proto-oncogenes are differentially expressed during embryonic development and may thus be important embryonic regulatory molecules. We report here that the products of two transforming oncogenes int-2 and hst/ks (now called kfgf) can, with different potencies, induce mesoderm formation in isolated Xenopus laevis animal pole explants and stimulate DNA synthesis in mammalian fibroblasts. The results suggest that these proteins may function as mesoderm inducers in mammalian embryogenesis and that similar receptor/signalling pathways may be utilized for developmental and oncogenic processes. Finally, we have shown that the Xenopus assay system used in this study provides a powerful screen for protein factors that are active in development.

99 EFFECT OF SUPPRESSION OF BOVINE DNA METHYLTRANSFERASE 1 ON EMBRYONIC DEVELOPMENT AND EXPRESSION OF IMPRINTED GENES

2009 ◽  
Vol 21 (1) ◽  
pp. 150
Author(s):  
P. Wilaiphan ◽  
F. Rings ◽  
M. Hoelker ◽  
E. Tholen ◽  
C. Phatsara ◽  
...  
Keyword(s):  
Embryonic Development ◽  
Protein Expression ◽  
Dna Methyltransferase ◽  
Critical Role ◽  
Apoptotic Index ◽  
Imprinted Genes ◽  
Dna Methyltransferase 1 ◽  
Relative Standard ◽  
Blastocyst Rate ◽  
Methyltransferase 1

DNA methyltransferase 1 (DNMT1) is believed to be involved in DNA methylation, which is a well-characterized epigenetic modulator shown to have essential functions in germ line and embryonic genome imprinting. This study was conducted to investigate the consequences of suppressing and inhibiting DNMT1 on the development, level of apoptosis, and expression of imprinted genes in pre-implantation bovine embryos. In vitro-produced zygotes were categorized into 4 groups; namely, those injected with Smartpool siRNA (SpsiRNA; Dharmacon Inc., Chicago, IL) (n = 800), 5aza-2′-deoxycytidine (5-AZA; Sigma, St. Louis, MO) (n = 864), nuclease-free water (n = 850), and uninjected control (n = 755). The mRNA expression data were generated using RT-PCR based on the relative standard curve method employing glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as a normalizer. Apoptotic index (API) was calculated by dividing the number of apoptotic cells to total cell number. The proportion of 2-, 4-, 8-cell and 2-, 4-, 8-, and 16-cell embryos was assessed 48 and 72 h, respectively, post-micro injection (pmi), whereas blastocyst rate was assessed at Day 8 pmi. Data on embryonic development and the relative mRNA abundance were analyzed using ANOVA followed by a multiple pair-wise mean comparison using Tukey test. The proportion of 2-, 4-, and 8-cell embryos at 48 h pmi was not significant among treatment groups. However, the proportion of the 8-cell embryos was significantly lower (P < 0.05) in SpsiRNA (16.3 ± 4.5) and 5-AZA injected groups (17.7 ± 4.9) compared with water-injected (26.8 ± 2.9) and uninjected controls (30.7 ± 6.2). The lowest total blastocyst rate (P < 0.05) was observed in the 5-AZA treatment group (16.9 ± 4.9) compared with SpsiRNA (23.4 ± 2.1) and water-injected (24.1 ± 5.3) and uninjected controls (29.4 ± 2.1). Microinjection of SpsiRNA reduced the target mRNA by 80 and 50% in 8-cell and blastocyst stage embryos, respectively, compared with uninjected control, and the protein expression level was also reduced at 8-cell embryos as confirmed by Western blotting. Injection of 5-AZA had no significant effect on mRNA or protein expression. The greatest API (P < 0.05) was found in SpsiRNA (4.2 ± 2.0) and 5-AZA (4.1 ± 1.7) injected groups compared with water-injected (2.8 ± 2.1) and uninjected controls (2.9 ± 2.3). The relative expression study also showed that microinjection of SpsiRNA and 5-AZA increased the expression of IGF2 (by 67 and 55%), IGF2R (29 and 30%), and IGFPB-4 (22 and 24%), respectively, compared with uninjected control, without affecting the expression of both IGF2R and IGFPB-4. In conclusion, suppression of DNMT1 resulted in lower proportion of 8-cell embryos, reduced blastocyst rate, and increased apoptotic index, and affected the expression of some imprinted genes, demonstrating a critical role of this gene in bovine embryonic development.

Mechanics of Embryonic Head Fold Morphogenesis

2008 ◽  
Author(s):  
Victor D. Varner ◽  
Dmitry A. Voronov ◽  
Larry A. Taber
Keyword(s):  
Embryonic Development ◽  
Incubation Period ◽  
Neural Plate ◽  
Vitelline Membrane ◽  
Heart Tube ◽  
Germ Layers ◽  
Embryonic Tissues ◽  
Anterior Extent ◽  
Insight Into ◽  
Embryonic Head

Head fold morphogenesis constitutes the first discernible epithelial folding event in the embryonic development of the chick. It arises at Hamburger and Hamilton (HH) stage 6 (approximately 24 hours into a 21-day incubation period) and establishes the anterior extent of the embryo [1]. At this stage, the embryonic blastoderm is composed of three germ layers (endoderm, mesoderm, and ectoderm), which are organized into a flat layered sheet that overlies the fibrous vitelline membrane (VM). Within this blastodermal sheet, a crescent-shaped head fold develops just anterior to the elongating notochord, spanning across the embryonic midline at the rostral end of neural plate. At the crest of this fold, the bilateral precardiac plates fuse in a cranial to caudal direction and give rise to the primitive heart tube and foregut [2, 3]. An understanding of head fold morphogenesis may thus offer insight into how embryonic tissues are arranged to make ready for proper cardiac formation.

scholarly journals siRNAs targeting terminal sequences of the SARS-associated coronavirus membrane gene inhibit M protein expression through degradation of M mRNA

2007 ◽  
Vol 145 (2) ◽  
pp. 146-154 ◽  
Author(s):  
Zhao-ling Qin ◽  
Ping Zhao ◽  
Ming-mei Cao ◽  
Zhong-tian Qi
Keyword(s):  
Protein Expression ◽  
M Protein ◽  
Membrane Gene

scholarly journals Temporal development of Drosophila embryos is highly robust across a wide temperature range

2018 ◽  
Author(s):  
Jeronica Chong ◽  
Christopher Amourda ◽  
Timothy E. Saunders
Keyword(s):  
Embryonic Development ◽  
Local Environment ◽  
Morphogen Gradient ◽  
Temporal Development ◽  
Developmental Systems ◽  
History Dependence ◽  
Wide Range ◽  
Different Temperatures ◽  
Species Specific ◽  
Drosophila Embryos

AbstractDevelopment is a precisely coordinated process in both space and time. Spatial precision has been quantified in a number of developmental systems, and, for example, such data has contributed significantly to our understanding of morphogen gradient interpretation. However, comparatively little quantitative analysis has been performed on timing and temporal coordination during development. Here, we use Drosophila to explore the temporal robustness of embryonic development within physiologically normal temperatures. We find that development is temporally very precise across a wide range of temperatures in all three Drosophila species investigated. However, we find temperature dependence in the heterochronicity. A simple model incorporating history-dependence can explain the developmental temporal trajectories. Interestingly, the history-dependence is temperature specific with either effective negative or positive feedback at different temperatures. We also find that embryos are surprisingly robust to shifting temperatures during embryogenesis. We further identify differences between tropical and temperate species that are suggestive of different potential mechanisms regulating temporal development depending on the local environment. Overall, our data shows that Drosophila embryonic development is temporally robust across a wide range of temperatures but there are species specific differences.

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