Gene expression is the process by which information from a gene is used to produce a functional product like proteins or RNA. It involves two main steps: transcription of DNA into mRNA and translation of mRNA into proteins. Transcription involves unwinding the DNA and synthesizing mRNA complementary to the template strand. Translation uses ribosomes to read the mRNA codon by codon and add the corresponding amino acids to produce a protein according to the genetic code. It occurs through three phases: initiation, elongation, and termination.
Gene regulation in eukaryotes in a nutshell covering all the important stages of gene regulation in eukaryotes at transcriptional level, translation level and post-translational level.
Most bacteria are free-living organisms that grow by increasing
in mass and then divide by binary fission.
Growth and division are controlled by genes, the expression
of which must be regulated appropriately. Genes
whose activity is controlled in response to the needs of a
cell or organism are called regulated genes. All organisms
also have a large number of genes whose products
are essential to the normal functioning of a growing and
dividing cell, no matter what the conditions are. These
genes are always active in growing cells and are known as
constitutive genes or housekeeping genes; examples include
genes that code for the enzymes needed for protein
synthesis and glucose metabolism. Note that all genes are
regulated on some level. If normal cell function is impaired
for some reason, the expression of all genes, including
constitutive genes, is reduced by regulatory
mechanisms. Thus, the distinction between regulated
and constitutive genes is somewhat arbitrary.
Gene regulation in eukaryotes in a nutshell covering all the important stages of gene regulation in eukaryotes at transcriptional level, translation level and post-translational level.
Most bacteria are free-living organisms that grow by increasing
in mass and then divide by binary fission.
Growth and division are controlled by genes, the expression
of which must be regulated appropriately. Genes
whose activity is controlled in response to the needs of a
cell or organism are called regulated genes. All organisms
also have a large number of genes whose products
are essential to the normal functioning of a growing and
dividing cell, no matter what the conditions are. These
genes are always active in growing cells and are known as
constitutive genes or housekeeping genes; examples include
genes that code for the enzymes needed for protein
synthesis and glucose metabolism. Note that all genes are
regulated on some level. If normal cell function is impaired
for some reason, the expression of all genes, including
constitutive genes, is reduced by regulatory
mechanisms. Thus, the distinction between regulated
and constitutive genes is somewhat arbitrary.
Riboswitches and RNA interference (RNAi)JanmoniBorah1
Riboswitches are the control buttons of mRNAs. They control the expression of gene by regulating transcription and translation.
Gene silencing by RNA interference is a mechanism of post transcriptional regulation of gene expression that involves mainly siRNA and miRNA.
This presentation is about the transcription machinery that is required for the transcription in eukaryotes. The comparison between the transcription factors involved in prokaryotes and eukaryotes. The initiation of transcription and how it helps in producing a mRNA.
Riboswitches and RNA interference (RNAi)JanmoniBorah1
Riboswitches are the control buttons of mRNAs. They control the expression of gene by regulating transcription and translation.
Gene silencing by RNA interference is a mechanism of post transcriptional regulation of gene expression that involves mainly siRNA and miRNA.
This presentation is about the transcription machinery that is required for the transcription in eukaryotes. The comparison between the transcription factors involved in prokaryotes and eukaryotes. The initiation of transcription and how it helps in producing a mRNA.
Enabling Accessible Resource Access via Service ProvidersAlexander Haffner
Libraries have become digitized and are using information technology for storing and managing their
resource inventory. Additional metadata are used for describing properties of non-digital assets as well
as of purely digital resources. In particular, as the amount of digital resources increases, there is
demand for centralized services for searching and distribution of content.
Stakeholders of libraries and publishing industry already have made progress in areas of archival
strategies and standardization of preservation strategies. A variety of metadata standards and
exchange protocols enable service providers to offer a single access point to resources. However,
there is still an increased demand for improvement of resource organization and enhanced quality
particularly in terms of accessibility. This paper presents strategies to increase accessibility of
resources as a valuable step towards access-for-all. For consideration of accessibility within the
publishing chain we analyse the whole processing chain and identify stakeholders such as national
libraries and their corresponding responsibilities for ingest, archival storage and dissemination of
digital resources.
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Protein synthesis and processing: Ribosome, formation of initiation complex, initiation factors and their regulation, elongation and elongation factors, termination, genetic code, aminoacylation of tRNA, tRNA-identity, aminoacyl tRNA synthetase, and translational proof-reading, translational inhibitors, Post Translational modification of proteins. Protein targeting.
It is the process of synthesis of protein by encoding information on mRNA.
Protein synthesis requires mRNA, tRNA, aminoacids, ribosome and enzyme aminoacyl tRNA synthase
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2. Gene expression
Gene expression is the process by which
information from a gene is used in the
synthesis of a functional gene product. These
products are often proteins, but in non-protein
coding genes such as transfer RNA
(tRNA) genes, the product is a functional RNA
according to the Cental Dogma.
3.
4. The Link Between DNA and Protein
• DNA contains the molecular blueprint of every
cell
• Proteins are the “molecular workers” of the cell
• Proteins control cell shape, function,
reproduction, and synthesis of biomolecules
• The information in DNA genes must therefore
be linked to the proteins that run the cell
5. The Genetic Code
• The base sequence in a DNA gene dictates the
sequence and type of amino acids in
translation
• Bases in mRNA are read by the ribosome in
triplets called codons
• Each codon specifies a unique amino acid in
the genetic code
• Each mRNA also has a start and a stop codon
6.
7.
8. Overview of Transcription
• Transcription of a DNA
gene into RNA has
three stages
– Initiation
– Elongation
– Termination
9. Initiation
• Initiation phase of transcription
1. DNA molecule is unwound and strands are
separated at the beginning of the gene
sequence
2. RNA polymerase binds to promoter region at
beginning of a gene on template strand
10.
11. Elongation
1. RNA polymerase synthesizes a sequence of
RNA nucleotides along DNA template strand
2. Bases in newly synthesized RNA strand are
complementary to the DNA template strand
3. RNA strand peels away from DNA template
strand as DNA strands repair and wind up
12.
13. Elongation
• As elongation proceeds, one end of the RNA
drifts away from the DNA; RNA polymerase
keeps the other end temporarily attached to
the DNA template strand
14.
15. Termination
– RNA polymerase reaches a termination
sequence and releases completed RNA strand
21. Translation
Translation is the process by which ribosomes read the genetic
message in the mRNA and produce a protein product according
to the message's instruction.
Figure 1.
23. Ribosomes
Eukaryotic ribosomes are larger. They consist of two
subunits, which come together to form an 80S particle.
60S subunit holds (three rRNAs 5S, 5.8S, 28S and about 40
proteins).
40S subunit contains (an18S rRNA and about 30 proteins).
Figure 2.
24. The large ribosomal subunit contains three tRNA binding sites,
designated A, P, and E.
The A site binds an aminoacyl-tRNA (a tRNA bound to an amino
acid).
P site binds a peptidyl-tRNA (a tRNA bound to the peptide
being synthesized).
The E site binds a free tRNA before it exits the ribosome.
Figure 3.
25. Steps for protein synthesis
First, aminoacyl tRNA synthetase joins amino acid to their
specific tRNA.
Second, ribosomes must dissociate into subunits at the end of
each round of translation.
26. The protein synthesis occur in 3 phases
Accurate and efficient initiation occurs; the ribosomes binds
to the mRNA, and the first amino acid attached to its tRNA.
Chain elongation, the ribosomes adds one amino acid at a
time to the growing polypeptide chain.
Accurate and efficient termination, the ribosomes releases
the mRNA and the polypeptide.
27. Initiation
The initiation phase of protein synthesis requires over 10
eukaryotic Initiation Factors (eIFs).
Factors are needed to recognize the cap at the 5'end of an
mRNA and binding to the 40s ribosomal subunit.
Binding the initiator Met-tRNAiMet (methionyl- tRNA) to the
40S small subunit of the ribosome.
Scanning to find the start codon by binding to the 5'cap of the
mRNA and scanning downstream until they find the first AUG
(initiation codon).
28. The start codon must be located and positioned correctly in
the P site of the ribosome, and the initiator tRNA must be
positioned correctly in the same site.
Once the mRNA and initiator tRNA are correctly bound, the
60S large subunit binds to form 80s initiation complex with a
release of the eIF factors.
29.
30. Elongation
Transfer of proper aminoacyl-tRNA from cytoplasm to A-site of
ribosome.
Peptide bond formation; Peptidyl transferase forms a peptide
bond between the amino acid in the P site, and the newly
arrived aminoacyl tRNA in the A site. This lengthens the
peptide by one amino acids.
Translocation; translocation of the new peptidyl t-RNA with
its mRNA codon in the A site into the free P site occurs. Now
the A site is free for another cycle of aminoacyl t-RNA codon
recognition and elongation.
32. Termination
Translation termination requires specific protein factors
identified as releasing factors, RFs in E. coli and eRFs in
eukaryotes.
The signals for termination are the same in both prokaryotes
and eukaryotes. These signals are termination codons present
in the mRNA. There are 3 termination codons, UAG, UAA and
UGA.
After multiple cycles of elongation and polymerization of
specific amino acids into protein molecules, a nonsense codon =
termination codon of mRNA appears in the A site.
33. The is recognized as a terminal signal by eukaryotic releasing
factors (eRF) which cause the release of the newly
synthesized protein from the ribosomal complex.
Figure 6.
34. Polysomes
Most mRNA are translated by more than one ribosome at a
time; the result, a structure in which many ribosomes
translate a mRNA in tandem, is called a polysomes.
Figure 7.
FIGURE 10-4b Transcription is the synthesis of RNA from instructions in DNA
A gene is a segment of a chromosome's DNA. One of the DNA strands will serve as the template for the synthesis of an RNA molecule with bases complementary to the bases in the DNA strand.
FIGURE 10-5 RNA transcription in action
This colorized electron micrograph shows the progress of RNA transcription in the egg of an African clawed toad. In each treelike structure, the central "trunk" is DNA (blue) and the "branches" are RNA molecules (red). A series of RNA polymerase molecules (too small to be seen in this micrograph) are traveling down the DNA, synthesizing RNA as they go. The beginning of the gene is on the left. The short RNA molecules on the left have just begun to be synthesized; the long RNA molecules on the right are almost finished.
FIGURE 10-4c Transcription is the synthesis of RNA from instructions in DNA
A gene is a segment of a chromosome's DNA. One of the DNA strands will serve as the template for the synthesis of an RNA molecule with bases complementary to the bases in the DNA strand.
FIGURE 10-4d Transcription is the synthesis of RNA from instructions in DNA
A gene is a segment of a chromosome's DNA. One of the DNA strands will serve as the template for the synthesis of an RNA molecule with bases complementary to the bases in the DNA strand.