ACTB
mRNA expression levels in lymphoblastic lines and fibroblasts derived from affected individuals were decreased in comparison to those in control cells.
Overall, parthenotes have similar
mRNA expression levels as IVF / ICSI embryos at the blastocyst stages (Figure 3 and 4B).
We also observed that parthenotes from in vitro matured oocytes have similar
mRNA expression levels of the majority of studied genes compared to IVF / ICSI embryos at the blastocyst stage.
Notably, a positive correlation between
the mRNA expression levels of DDX3 and p21waf1 / cip1 in 45 HCC specimens was also found by linear regression analysis (r = 0.501, P < 0.001; Fig. 5D).
E: Comparison of
mRNA expression levels in adipose tissue from nonobese (BMI < 30 kg / m2, n = 40) and obese (BMI > 30 kg / m2, n = 30) NGT subjects.
High
mRNA expression levels of HNF4α and ASGPR1 are shown in the enhanced hiPS - HEP cells for an extended culture time and are comparable to levels in cryopreserved human primary hepatocytes (hphep cells) that have been grown for only a short time.
cDNA synthesized by reverse transcription of 1 µg RNA primed with oligo (dT) and random 9 - mer primers was used as the substrate for quantitation of
mRNA expression levels by quantitative RT — PCR in the presence of SYBR ® Green (Stratagene, La Jolla, CA).
Consistent with low
mRNA expression levels, neither the Xpd † XPCS nor the Xpd † XP allele was able to restore TFIIH abundance to wt levels in XpdTTD compound heterozygote cells (Figure 4E and 4F).
Alterations of methylation status and
mRNA expression levels of RARβ, MGMT, p16, or hMLH1 genes after treatment with EGCG or other polyphenols.
For each gene, the top panel presents the unmethylation - specific bands (UMSB), the middle panel presents the methylation - specific bands (MSB), and the bottom panel presents
the mRNA expression levels (mRNA).
The average
mRNA expression level of morulas (A) and blastocysts (B) from parthenogenesis and IVF / ICSI were displayed.
Not exact matches
To investigate, they measured
mRNA levels associated with the
expression of 23,000 genes in human brain tissue.
Unlike most biomarkers for cancer, DDX3
mRNA expression only increased slightly in the exposed breast cells, but the corresponding proteins
levels were significantly higher.
The
expression of
mRNA for factors involved in promoting mitochondrial biogenesis, including the transcription factor Ppard, the PPARδ coactivator Pgc - 1α, and citrate synthase was greater in gastrocnemius muscles from IL - 15Rα — KO relative to B6129 control (Figure 5C); however,
levels of these genes were unchanged in spleen and kidney (data not shown).
In addition, gastrocnemius muscles from IL - 15Rα — KO mice expressed higher
levels of
mRNA for the sarcoplasmic endoplasmic reticulum calcium ATPase - II (SERCA2) and lower
mRNA expression and protein content of the calcium - binding protein calsequestrin (Figure 5, F and G).
Besides, researchers have also collected very large molecular datasets linked to gene
expression in different organs of BXD mice, such as
levels of
mRNA, proteins, and metabolites.
The muscles from IL - 15Rα — KO mice had a greater relative
expression of the SERCAII isoform and lower
mRNA and protein
levels of calsequestrin, both characteristic of slow muscles (52).
For example, hypoxia has been reported to induce VEGF
expression in the retina, both at the
mRNA [16,17] and protein
levels [16].
In contrast, the
level of XPCS
mRNA expression did affect the ability of the encoded protein (XPDG602D) to restore the TTD hair phenotype to normal.
Despite reduced
levels of
mRNA expression, the homozygous lethal Xpd † XPCS allele ameliorated multiple XpdTTD - associated disease symptoms in compound heterozygous XpdTTD / † XPCS animals including the hallmark brittle hair and cutaneous features fully penetrant in homo - and hemizygous TTD mice (Figure 2A — 2C).
The defect in SMN2 gene
expression in SMA patients is at the
level of premRNA splicing, such that exon 7 tends to be left out of the
mRNA that ultimately makes SMN protein.
mRNA expression from the targeted allele could be detected in embryonic stem cells by RT - PCR (Figure 1D), although
expression was reduced approximately 5-fold relative to wt
mRNA transcript
levels as determined by Northern blotting of RNA from the testis of heterozygous animals (Figure 1E).
Finally,
mRNA expression of striatal tissue found no differences in BDNF
expression although
expression of TNF - in the 3 - NP - iPSC - 21 and -42 rats had significantly lower
levels than sham control and 3 - NP - iPSC - 7 rats, suggesting that there was not a continuous immune response to iPSCs.
Expression levels of DDX3
mRNA in HCC samples as shown in (B) are classified into unchanged, decreased, and enhanced categories.
The
expression levels of AtRCCR and AtChlase from the same PlantPho promoter differ, possibly from differences in
mRNA stability for AtRCCR and AtChlase.
Although there was no effect in the null mutant, we found ilp2
mRNA expression increased and AKT
expression level was down regulated in larvae where either TOR signaling activity or the
expression of GBP1 and GBP2 was specifically reduced in the fat body.
Proteomics — the large - scale study of proteins, particularly their structure and function — combined with transcriptomics — the examination of the
expression level of messenger ribonucleic acids (
mRNAs) in a given cell population - played a significant role in the recent derivation of a combined protein and gene list that constitutes one of the largest descriptive data sets of its kind.
Silencing of Nrf2 significantly decreased baseline
levels of HMOX1, whereas silencing of Bach1 resulted in a 50-fold increase in
expression of HMOX1
mRNA (Figure 4B).
As shown in Fig 5D, dilp5
mRNA levels were significantly reduced in CCHa2 - knockdown larvae, indicating that peripheral tissue - derived CCHa2 activates dilp5
expression in the brain.
Specifically, a mouse paradigm that mimics binge alcohol drinking in humans produced a robust reduction in BDNF
mRNA levels in the medial PFC (mPFC), which was associated with increased
expression of several miRNAs including miR - 30a - 5p.
His group uses high - throughput genomic methods — including DNA sequencing, genotyping, chromatin immunoprecipitation,
mRNA expression profiling, transcriptional promoter and DNA methylation measurements — as well as computational and statistical tools to identify, characterize and understand the functional elements encoded in our genomes and how they work together at the molecular
level in normal and pathological conditions.
To directly measure the
level of coordination in the
expression of genes, we used highly sensitive fluorescence in situ hybridization (FISH) to count individual
mRNAs of functionally related and unrelated genes within single Saccharomyces cerevisiae cells.
mRNA molecules contain the instructions for making proteins — the number of
mRNAs from a given gene is a measure of the
level of
expression of that gene.
Kayla Coldsnow, a Rensselaer doctoral student and the first author on the study, tracked the
expression of the
mRNA of PER in Daphnia exposed to naturally low salt
levels and constant dark conditions.
Interestingly, while high
levels of fluorescence and the
expression of Hex and Cerberus
mRNA required activin, low
levels of Venus fluorescence were detected in the absence of activin.
The detection of this
level of Venus
expression in the presence of low
levels of Hex
mRNA suggests that this reporter is indeed extremely sensitive to the low
levels of Hex transcript produced in the absence of activin, earlier in differentiation, and in undifferentiated ES cells.
Home > Press > Single - cell
mRNA cytometry via sequence - specific nanoparticle clustering and trapping: Cell - to - cell variation in gene
expression creates a need for techniques that can characterize
expression at the
level of individual cells
MEIS1 intronic risk haplotype associated with restless legs syndrome affects its
mRNA and protein
expression levels.
In some cases affected transcripts in Cre +; Tsc1 flox / flox mice showed significant variation among individuals that can not simply be explained by differential effectiveness of CRE - mediated knockout since, except one animal, all Cre +; Tsc1 flox / flox mice showed similarly reduced
expression levels of Tsc1
mRNA.
(B) Liver
expression of Apoc3
mRNA levels in mutant mice on a high - fat diet for 6 weeks and treated for the last 5 weeks with control or ApoC - III ASO (n = 3 — 7 / group).
Treatment of iLpldf mice with ApoC - III ASO decreased Apoc3
mRNA levels (Figure 8A) and protein
expression (Supplemental Figure 6A) and reduced plasma TGs (Figure 8B) and TGs in CR / VLDL particles (Figure 8C).
Compared to PHWSC adipocytes, SGBS adipocytes showed not only greater induction of adipogenic gene
expression during differentiation but also increased
levels of UCP1
mRNA and protein
expression.
Analysis of Oct4 protein
expression in differentiated Ara - C cultures (DACs) showed a slight increase of Oct4 protein by day four of aggregate formation (Figure 1C), consistent with previous reports examining Oct4
mRNA dynamics [22] and the finding that primitive endoderm differentiation is accompanied by a transient increase in Oct4 protein
levels [23].
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.
The co ‐
expression of neighboring genes at the
mRNA level is driven by chromatin fluctuations and direct regulatory interference.
Other studies at the molecular
level have shown Berberine changes the
expression of PPARgamma2
mRNA genes to inhibit formation of adipocytes (fat cells)(19, 20).
MuRF - 1
mRNA expression was elevated 2 h following exercise but had returned to basal
levels, by 8 h in all treatments.
The Clock mutants were also shown to exhibit reduced overall
expression levels and a blunted diurnal rhythm of orexin
mRNA, a hypothalamic neuropeptide involved in energy regulation (2).
Robust changes in
expression of brain - derived neurotrophic factor (BDNF)
mRNA and protein across the brain do not translate to detectable changes in BDNF
levels in CSF or plasma.