Brusatol overcomes chemoresistance through inhibition
of protein translation.
While it has been understood for some time now that tRNAs are heavily decorated with small chemical groups such as methyls (carbon atoms bound to three hydrogens), the unprecedented discovery that one of these modifications can be removed suggests that tRNA has a regulatory role in the process
of protein translation through chemical changes in itself.
There are two sets
of protein translation systems in mammalian cells — the cytoplasmic translation system and the mitochondrial translation system — both of which are composed of ribosome, tRNAs and translation factors.
Not exact matches
Whey
Protein Concentrate, hidden under the flap, is one
of the first ingredients (
translation: there is a decent dose
of whey in this product).
Now, new research from the University
of Maryland School
of Medicine (UM SOM), has identified a crucial
protein in this
translation process.
The actions
of this topogenic sequence were independent
of on - going
translation and could be conferred to heterologous
proteins by the engineering
of a discrete set
of codons.
Glo's ability to repress nanos
translation during egg development required both
of the
protein's RNA - binding modes.
This
protein was originally identified due to its ability to repress the
translation of an RNA molecule called nanos to
protein in fly eggs.
Biosynthetic studies
of the prion
protein (PrP) have shown that two forms
of different topology can be generated from the same pool
of nascent chains in cell - free
translation systems supplemented with microsomal membranes.
The gene is involved in the
translation of proteins from RNA and in the proliferation and migration
of neurons in the brain.
Both are involved in the
translation of proteins from RNA.
The pilot project tested a dozen or so
of the most commonly used gene promoters (regions
of DNA that facilitate gene transcription) and segments
of DNA that encode ribosome - binding sites (sequences
of messenger RNA that control
protein translation) to determine whether they behave consistently in different cellular contexts.
The remaining 90 or so characterized
proteins include molecular chaperones, which prevent other
proteins from sticking together;
translation machinery, which coaxes messenger RNAs and ribosomes to form
proteins; and
proteins that control the structure
of RNA.
For most known genes this «messenger» or mRNA is then shuttled off to a ribosome
of a cell where its
translation into a
protein sequence occurs.
MicroRNAs are a class
of short, non-coding RNAs that regulate the
translation or degradation
of messenger RNA and therefore the
proteins that cells make.
They also searched for sequences that enhance the efficiency
of translation, when RNA messages are interpreted to build products such as
protein molecules.
Moreover, within Mimi's outsize helping
of genetic material, Claverie found genes for such things as the
translation of proteins, DNA repair enzymes, and other types
of protein.
With no nucleus to further modify and craft gene expression and
protein translation, life thrived but literally could not get hold
of itself, could not assume new shapes or diversify.
Erythromycin targets bacterial ribosomes — the nanomachine responsible for the
translation of messenger RNA (mRNA) sequences into
protein — thus preventing synthesis
of the
proteins required for continued growth and survival.
The team confirmed that guanabenz acts by temporarily blocking the reactivation
of a
protein known as eukaryotic
translation initiation factor 2 (eIF2α).
HCV invades cells in the body by binding to specific receptors on the cell, enabling the virus to enter it.2 Once inside, HCV hijacks functions
of the cell known as transcription,
translation and replication, which enables HCV to make copies
of its viral genome and
proteins, allowing the virus to spread to other sites
of the body.2 When HCV enters the host cell, it releases viral (+) RNA that is transcribed by viral RNA replicase into viral -LRB--) RNA, which can be used as a template for viral genome replication to produce more (+) RNA or for viral
protein synthesis.
RNA serves as the template for
translation of genes into
proteins, transferring amino acids to the ribosome to form
proteins, and also translating the transcript into
proteins.
Incorporating
protein and mRNA turnover data in this analysis, the results from Li et al. suggest that mRNA levels explain ~ 81 %
of the variance in
protein levels, transcription 71 %, RNA degradation 10 %;
translation 11 %; and
protein degradation 8 %.
This process enables the virus to take advantage
of the host cell's
protein translation machinery for its own purposes.
Researchers have ignored these noncoding RNAs until recently for not complying with the central dogma
of biology — that a straight line runs from gene to RNA (transcription) to
protein (
translation).
Ribosomes are the molecular machines responsible for the
translation of mRNA sequences into the amino - acid sequences
of the specified newly synthesized
protein.
As the
translation machinery is limiting, the energy - intensive production
of new
proteins is overall dampened.»
Furthermore, there are ways to inhibit
translation of a gene into a
protein.
In addition to determining that
protein aggregation is regulated and requires active
translation, Stowers scientists revealed that the mitochondria, the cell's powerhouses, play a key role in the mobility
of these
protein aggregates.
Through closer investigation, he found that the RNA sections that stuck around contained chemical codes that act as stop signs, prematurely halting the
translation of the RNA from these two genes into
proteins.
MicroRNAs (miRNA) are a class
of noncoding RNAs with lengths
of approximately 22 nucleotides that bind to target messenger RNAs to inhibit
protein translation.
Cells may use different rates
of translation in different types
of mRNA to produce the right amounts and ratios
of required
proteins.
A drug blocking this binding
protein could shut off
translation of only the growth - promoting
proteins and not other life - critical
proteins inside the cell.
In 2012, a group from the RIKEN Center for Life Science Technologies, in collaboration with SISSA, an Italian University, discovered a new class
of mouse lncRNAs, which are called «antisense» because their can pair with typical
protein - coding mRNAs and enhance their
translation.
Before, that
protein was thought to be just one
of a dozen or so general initiation factors required for mRNA
translation.
Because
of their central importance to biology,
proteins have been the focus
of intense research, particularly the manner in which they are produced from genetically coded templates — a process commonly known as
translation.
While the general mechanism
of translation has been understood for some time,
protein synthesis can initiate by more than one mechanism.
This leads to degradation
of «viral» RNA, preventing its
translation on ribosomes into a
protein encoded by it, thereby reducing the viral gene expression,» says one
of the main co-authors
of the research Alexander Timin, a JRF
of the Novel Dosage Laboratory at Tomsk RASA Center.
Importantly, Zika virus also follows the same pattern
of cellular behavior
of repressing the cell's
translation and stress response while promoting its own
protein translation.
Previous studies in the Eberwine lab have shown that
translation of messenger RNAs (mRNAs) into
proteins occurs in dendrites at focal points called translational hotspots.
Additionally, laboratories around the world are working to develop SINEUPs to enhance
protein translation as a therapy for specific diseases caused by the deficiency
of a specific
protein, such a haploinsufficiencies, where one
of two genes is not functional.
Scientists have found a group
of human sequences — unrelated to those in mice — which are capable
of producing SINEUPs, which can pair with typical
protein - coding mRNAs and enhance their
translation.
«This is the first time this method
of protein labeling has been used to measure the act
of translation of multiple
proteins over space and time in a quantitative way,» says Eberwine.
«We know from previous studies that the fission yeast version
of DDX3X is thought to play a role in
translation of key regulatory
proteins, possibly by helping untangle parts
of the RNA molecule.»
The unique ability among them to encode
proteins involved in
translation (typically DNA to RNA to
protein) piqued researchers» interests as to the origin
of giant viruses.
A rare, but synonymous, codon in alleles
of a drug - resistance gene can change
translation kinetics and so produce a conformationally distinct
protein species.
This includes how subtle changes in gene sequences can impact the expression
of encoded
proteins through mechanisms including codon bias, mRNA stability, and
translation initiation.
To visualize
translation, Dr. Singer and his colleagues took advantage
of a key occurrence during the first round
of translation: the ribosome to which mRNAs attach must displace so - called RNA - binding
proteins from the mRNAs.
Environmental factors interact with the different subgenomes to modify the transcription
of their component genes and to modulate the
translation of protein products and their posttranslational modification, yielding changes in
protein and cellular function and metabolism, and defining an intermediate phenotype.
New research by scientists from the University
of Chicago demonstrates that the mammalian enzyme ALKBH1 can remove molecular modifications from transfer RNA, causing a measurable effect on
protein translation in the cell.