This tendency of the association of the lipid containing structures with nuclear periphery can be seen also during later developmental stages in
wild type embryos (D).
These large lipid - containing structures were observable in live mutant embryos (Fig. 4J) but not in
wild type embryos (Fig. 4K) using Nomarski optics.
(C) Lipid containing structures localize around the nucleus in one cell
wild type embryos.
Despite the fact that there were a larger number of individually recognizable lipid containing structures in
wild type embryos (Fig. 6D), the mean area of these structures in mutants was considerably larger (Fig. 6C).
Analysis for embryos was done on images of seven different embryos (seven mutant and seven
wild type embryos) inside gravid hermaphrodites (only one and two cell early embryonic stages were chosen for comparison).
(G) Shows
a wild type embryo at later stage of the development.
Not exact matches
An organ called Kupffer's vesicle, which helps specify the left and right sides of the developing fish, is shaped asymmetrically in a
wild -
type embryo (left), but is more symmetric in the absence of maternally inherited gdf3 (right).
Endogenous CED - 9 and CED - 4 proteins localized to mitochondria in
wild -
type embryos, in which most cells survive.
Most notably, the studies are based on transient transfection of
wild -
type and mutant gene constructs into cultured cells or into zebrafish
embryos and are unlikely to reproduce the specific mutant gene dose that is present in heterozygous mutant cells in FOP patients.
Compared with
wild -
type embryos (A), uninjected alk8 — / —
embryos are weakly (class 2; C2) dorsalized (B), with loss of the ventral fin fold (arrowheads).
(G — L) In situ hybridization of
wild -
type embryos injected with
wild -
type (G — I) or mutant ACVR1 (J — L) to detect ventral markers eve1 (G, n = 12/12; J, n = 10/13; onset of gastrulation) and gata2 (H, n = 14/14; K, n = 15/19; mid-gastrulation) or dorsal marker foxb1.2 (I, n = 12/12; L, n = 6/13, 7/13 showed no expression; mid-gastrulation).
Injection of
wild -
type stage 15
embryos with E. coli constitutively expressing Mcf1 from the high - copy vector pUC18 causes rapid paralysis of embryonic hemocytes and inhibition of phagocytosis as observed following
wild -
type Photorhabdus infection (Figure 3A and Video S3).
Microinjection of
wild -
type human ACVR1 RNA into alk8 — / — zebrafish
embryos rescued approximately 80 % of the injected
embryos completely or partially (Figure 3, C and F), showing that human ACVR1 can function as a BMP
type I receptor in this zebrafish model and substitute for Alk8.
In contrast to
embryos, lipid - containing structures in enterocytes and in epidermal cells of adult animals are smaller in mutants than in
wild type animals.
Therefore, we transplanted embryonic eye fields from YFP transgenic
embryos to
wild -
type hosts.
In transient transgenic reporter studies of zebrafish
embryos, the +254 kb element holds up: the
wild -
type allele had enhancer activity in 41/82
embryos (50 %), whereas the mutant allele had enhancer activity in 3/83
embryos (3.6 %).
For experiments requiring complete eye field replacement (A and B), one half of the eye field was surgically removed from
wild -
type, stage 15 (host)
embryos, and replaced with the donor cells from one half of an explant.
The goal of this protocol (written in French) is to describe the steps and quality controls to prepare new stable murine embryonic stem cells lines: ① either from
wild type mouse
embryos to introduce a mutation by genetic targeting or homologous recombination to get a genetically modified mouse line ② or from genetically modified mouse
embryos with two aims:
On fixed
embryos stained with LipidTox, larger than
wild type lipid droplets are visible until late embryonic stages, including three fold
embryos.
A 250 - µm2 region of LE or the left eye field was removed from stage 15
wild -
type host
embryos [38] using a Gastromaster.
MEFs from Brctx - deficient
embryos grow at a similar rate to
wild -
type MEF CD4 / CD8 expressions, and the cell cycle parameters of thymocytes from
wild -
type and Brctx knockout animals are indistinguishable.
By injecting pairs of TALEN - encoding mRNAs into
wild -
type embryos, we generated the CCHa2 - RTAL - 34 frameshift allele (Figs 3B and S2B and S2C).
(C — F) Expression patterns of tailless (tll; C and D) and huckebein (hkb; E and F) in
wild -
type (C and E) and psqrum (D and F) early
embryos.
(A and B) Cuticle phenotype of
embryos from
wild -
type and psqrum homozygous females.
(A — D) Immunostaining with an anti-Vas antibody in
embryos from
wild -
type (A and B) and psqrum (C and D) females.
In situ hybridizations of
wild -
type and mutant
embryos or ovaries were developed in parallel.
While Vas levels in early psqrum mutants appear similar to those of
wild -
type embryos, the number of pole cells is strongly reduced.
As in the
embryo cryopreservation procedure, we will archive 200
embryos from a heterozygous x
wild -
type mating and 100
embryos from a homozygous x
wild -
type mating.
(D) Quantitative RT - PCR determination of BMP12 expression in body and neck skin of E7.5 and E8.5
wild type and Na / Na
embryos.
After three days, they tested each cell in every
embryo to learn how many had two copies of the
wild -
type allele.
To determine what aspects of mesodermal cell migration are affected in toddler mutants, we tracked migrating drl: eGFP - positive ventrolateral mesodermal cells (Mosimann et al., 2015) in
wild -
type and toddler mutant
embryos during gastrulation using light sheet microscopy (Figure 5C and Video 1).
All
embryos were stage matched and transplantations were homotypic:
wild type into
wild type or toddler mutant into toddler mutant.
These human
embryos almost always used the
wild -
type strand on the healthy allele to guide the repair, rather than the introduced ssODN.
Antibody staining also shows increased phosphorylation of the Nodal signal transducer, Smad2, in lefty2 mutant
embryos as compared to
wild -
type embryos (Author response image 1)(Dubrulle et al. 2015; Schier 2009).
(C) Representative still frames of maximum intensity projections from a
wild -
type and toddler mutant drl: eGFP transgenic
embryo.
But given the clear differences between toddler mutants and
wild -
type embryos, a more detailed measurement is unlikely to affect the conclusions drawn from this experiment.
Third,
wild -
type and toddler mutant
embryos were injected at the one cell stage with increasing levels of Nodal mRNA and Nodal target gene expression was measured just prior to gastrulation using qRT - PCR.