The delivery of newly synthesized protein to their proper cellular destination, usually referred to as protein targeting or sorting.
The mode of protein transport depends chiefly on the location in the cell cytoplasm of the polysomes involved in protein synthesis.
There are two modes of protein sorting:-
1) Co - translational Transportation.
2) Post - translational Transportation.
The delivery of newly synthesized protein to their proper cellular destination, usually referred to as protein targeting or sorting.
The mode of protein transport depends chiefly on the location in the cell cytoplasm of the polysomes involved in protein synthesis.
There are two modes of protein sorting:-
1) Co - translational Transportation.
2) Post - translational Transportation.
CBCS 4TH SEM ,
CHARGING, STRUCTURE AND FUNCTION OF tRNA,
AMINOACYL RNA SYNTHETASE(ASR) PROOFREADING AND EDITING
https://www.youtube.com/watch?v=YzOVMWYLiCE
despite of the enormous genomic diversity, the phage genome mapping is being done using a plethora of techniques,which includes both genetic mapping and physical mapping
Dna supercoiling and role of topoisomerasesYashwanth B S
supercoiling is one of the important process to condenses the huge amount of DNA to fit inside the histone and its also plays a role during the replication ,transcription etc..,these activities is carried out by an enzyme called topoisomerases.
CBCS 4TH SEM ,
CHARGING, STRUCTURE AND FUNCTION OF tRNA,
AMINOACYL RNA SYNTHETASE(ASR) PROOFREADING AND EDITING
https://www.youtube.com/watch?v=YzOVMWYLiCE
despite of the enormous genomic diversity, the phage genome mapping is being done using a plethora of techniques,which includes both genetic mapping and physical mapping
Dna supercoiling and role of topoisomerasesYashwanth B S
supercoiling is one of the important process to condenses the huge amount of DNA to fit inside the histone and its also plays a role during the replication ,transcription etc..,these activities is carried out by an enzyme called topoisomerases.
Chromosomes in most of the bacteria are single circular DNA molecule which are Haploid
Exceptions include:
Bacteria with linear chromosomes
Bacteria with more than one chromosome
DNA organization or Genetic makeup in Prokaryotic and Eukaryotic SystemsBir Bahadur Thapa
DNA organization or Genetic makeup in Prokaryotic and Eukaryotic Systems!! It is prepared under the syllabus of Tribhuwan University, Nepal, MSc. 3rd Semester as a lecture class!!
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
Earliest Galaxies in the JADES Origins Field: Luminosity Function and Cosmic ...Sérgio Sacani
We characterize the earliest galaxy population in the JADES Origins Field (JOF), the deepest
imaging field observed with JWST. We make use of the ancillary Hubble optical images (5 filters
spanning 0.4−0.9µm) and novel JWST images with 14 filters spanning 0.8−5µm, including 7 mediumband filters, and reaching total exposure times of up to 46 hours per filter. We combine all our data
at > 2.3µm to construct an ultradeep image, reaching as deep as ≈ 31.4 AB mag in the stack and
30.3-31.0 AB mag (5σ, r = 0.1” circular aperture) in individual filters. We measure photometric
redshifts and use robust selection criteria to identify a sample of eight galaxy candidates at redshifts
z = 11.5 − 15. These objects show compact half-light radii of R1/2 ∼ 50 − 200pc, stellar masses of
M⋆ ∼ 107−108M⊙, and star-formation rates of SFR ∼ 0.1−1 M⊙ yr−1
. Our search finds no candidates
at 15 < z < 20, placing upper limits at these redshifts. We develop a forward modeling approach to
infer the properties of the evolving luminosity function without binning in redshift or luminosity that
marginalizes over the photometric redshift uncertainty of our candidate galaxies and incorporates the
impact of non-detections. We find a z = 12 luminosity function in good agreement with prior results,
and that the luminosity function normalization and UV luminosity density decline by a factor of ∼ 2.5
from z = 12 to z = 14. We discuss the possible implications of our results in the context of theoretical
models for evolution of the dark matter halo mass function.
Remote Sensing and Computational, Evolutionary, Supercomputing, and Intellige...University of Maribor
Slides from talk:
Aleš Zamuda: Remote Sensing and Computational, Evolutionary, Supercomputing, and Intelligent Systems.
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Inter-Society Networking Panel GRSS/MTT-S/CIS Panel Session: Promoting Connection and Cooperation
https://www.etran.rs/2024/en/home-english/
Toxic effects of heavy metals : Lead and Arsenicsanjana502982
Heavy metals are naturally occuring metallic chemical elements that have relatively high density, and are toxic at even low concentrations. All toxic metals are termed as heavy metals irrespective of their atomic mass and density, eg. arsenic, lead, mercury, cadmium, thallium, chromium, etc.
Phenomics assisted breeding in crop improvementIshaGoswami9
As the population is increasing and will reach about 9 billion upto 2050. Also due to climate change, it is difficult to meet the food requirement of such a large population. Facing the challenges presented by resource shortages, climate
change, and increasing global population, crop yield and quality need to be improved in a sustainable way over the coming decades. Genetic improvement by breeding is the best way to increase crop productivity. With the rapid progression of functional
genomics, an increasing number of crop genomes have been sequenced and dozens of genes influencing key agronomic traits have been identified. However, current genome sequence information has not been adequately exploited for understanding
the complex characteristics of multiple gene, owing to a lack of crop phenotypic data. Efficient, automatic, and accurate technologies and platforms that can capture phenotypic data that can
be linked to genomics information for crop improvement at all growth stages have become as important as genotyping. Thus,
high-throughput phenotyping has become the major bottleneck restricting crop breeding. Plant phenomics has been defined as the high-throughput, accurate acquisition and analysis of multi-dimensional phenotypes
during crop growing stages at the organism level, including the cell, tissue, organ, individual plant, plot, and field levels. With the rapid development of novel sensors, imaging technology,
and analysis methods, numerous infrastructure platforms have been developed for phenotyping.
Deep Behavioral Phenotyping in Systems Neuroscience for Functional Atlasing a...Ana Luísa Pinho
Functional Magnetic Resonance Imaging (fMRI) provides means to characterize brain activations in response to behavior. However, cognitive neuroscience has been limited to group-level effects referring to the performance of specific tasks. To obtain the functional profile of elementary cognitive mechanisms, the combination of brain responses to many tasks is required. Yet, to date, both structural atlases and parcellation-based activations do not fully account for cognitive function and still present several limitations. Further, they do not adapt overall to individual characteristics. In this talk, I will give an account of deep-behavioral phenotyping strategies, namely data-driven methods in large task-fMRI datasets, to optimize functional brain-data collection and improve inference of effects-of-interest related to mental processes. Key to this approach is the employment of fast multi-functional paradigms rich on features that can be well parametrized and, consequently, facilitate the creation of psycho-physiological constructs to be modelled with imaging data. Particular emphasis will be given to music stimuli when studying high-order cognitive mechanisms, due to their ecological nature and quality to enable complex behavior compounded by discrete entities. I will also discuss how deep-behavioral phenotyping and individualized models applied to neuroimaging data can better account for the subject-specific organization of domain-general cognitive systems in the human brain. Finally, the accumulation of functional brain signatures brings the possibility to clarify relationships among tasks and create a univocal link between brain systems and mental functions through: (1) the development of ontologies proposing an organization of cognitive processes; and (2) brain-network taxonomies describing functional specialization. To this end, tools to improve commensurability in cognitive science are necessary, such as public repositories, ontology-based platforms and automated meta-analysis tools. I will thus discuss some brain-atlasing resources currently under development, and their applicability in cognitive as well as clinical neuroscience.
2. Bacterial Chromosomes
•A typical prokaryote has a single circular chromosome containing all (or most)
of the genes found inside the cell.
•Although a single chromosome is the rule among prokaryotes, there are
exceptions. A few prokaryotes contain two chromosomes.
3. The Escherichia coli Chromosome
•Today, many bacterial genomes, including that of Escherichia coli, have been completely
sequenced, thus revealing the number and location of the genes they possess.
• However, the genes of E. coli were initially mapped long before sequencing was
performed, using conjugation and transduction.
• Map distances are given in “minutes” of transfer that derive from conjugation
experiments, with the entire chromosome containing 100 minutes (or centisomes).
• Zero is arbitrarily set at thrABC (the threonine operon), because the
thrABC genes were the first shown to be transferred by conjugation in E. coli.
• The size of the chromosome is given in both minutes and in kilobase pairs of DNA.
4. •The strain of E. coli whose chromosome was originally sequenced, strain
MG1655, is a derivative of E. coli K-12, the traditional strain used for genetics.
•Wild-type E. coli K-12 has bacteriophage lambda integrated into its chromosome
and also contains the F plasmid. However, strain MG1655 had both of these
removed before sequencing (lambda by radiation and the F plasmid by acridine
treatment).
•The chromosome of strain MG1655 contains 4,639,221 bp. Analysis revealed
4288 possible protein-encoding genes that account for about 88% of the genome.
• Approximately 1% of the genome consists of genes encoding tRNAs and rRNAs.
Regulatory sequences—promoters, operators, origin and terminus of DNA
replication, and so on— comprise around 10% of the genome. The remaining 0.5%
consists of noncoding, repetitive sequences
5. Replication proceeds bidirectionally from the origin of DNA replication, oriC, at 84.3
min. The inner circle shows the locations, in kilobase pairs, of the sites where the
restriction enzyme NotI cuts.
The origins and directions of transfer of a few Hfr strains are also shown
(arrows). The
locations of five copies of the transposable element IS3 found in a particular
The site where bacteriophage lambda integrates is shown in red. If lambda were
present, it would add an extra 48.5 kbp (slightly over 1 min) to the map.
The genes of the maltose regulon, which includes several operons, are indicated by green
labels. The maltose genes are abbreviated mal except for lamB, which encodes an outer
membrane protein for maltose uptake that is also the receptor for bacteriophage lambda.
The gene rpsL (73 min) encodes a ribosomal protein. This gene was once called str because
mutations in it lead to streptomycin resistance
6. Arrangement of Genes on the Escherichia coli Chromosome
•Genetic mapping of the genes that encode the enzymes of a single biochemical
pathway in E. coli has shown that these genes are often clustered.
Notice, for instance, the gal gene cluster at 18 min, the trp gene cluster at about 28
min, and the his cluster at 44 min.
Each of these gene clusters constitutes an operon that is transcribed as a single
mRNA carrying multiple coding sequences, that is, a polycistronic mRNA.
Genes for some other biochemical pathways in E. coli are not clustered. For example, genes
for arginine biosynthesis (arg genes) are scattered throughout the chromosome.
7. •The early discovery of multigene operons and their use in studying gene regulation
(for example, the lac operon) often gives the impression that such operons are the
rule in prokaryotes.
•However, sequence analysis of the E. coli chromosome has shown that over 70% of
the 2584 predicted or known transcriptional units contain only a single gene.
•Only about 6% of the operons have four or more genes.
8. In E. coli the transcription of some genes proceeds clockwise around the
chromosome, whereas transcription of others proceeds counterclockwise.
This means that some coding sequences are on one strand of the chromosome
whereas others are on the opposite strand.There are about equal numbers of genes on both strands. The direction of
transcription of a few multigene operons is shown by the arrows in Figure.
Many genes that are highly expressed in E. coli are oriented so that they are
transcribed in the same direction that the DNA replication fork moves through them.
9. The two replication forks start at the origin, oriC located at about 84 min, and move
in opposite directions around the circular chromosome toward the terminus, which is
located at approximately 34 min.
•All seven of the rRNA operons of E. coli and 53 of its 86 tRNA genes are transcribed in
the same direction as replication.
All seven of the rRNA operons of E. coli and 53 of its 86 tRNA genes are transcribed in
the same direction as replication.Presumably, this arrangement for highly expressed genes allows RNA polymerase to
avoid collision with the replication fork, because this moves in the same direction as
the RNA polymerase.
10. • Although E. coli has very few duplicate genes, computer analyses have shown that
many of its protein-encoding genes arose by gene duplication during evolutionary
history.
•The E. coli genome also contains some large gene families— groups of genes with
related sequences encoding products with related functions.
•For example, there is a family of 70 genes that all encode membrane transport
proteins. Gene families are common, both within a species and across broad
taxonomic lines.
•Thus gene duplication plays a major role in evolution.
11. Insertions within the Escherichia coli Chromosome and Horizontal Gene Transfer
•Several other genetic elements are inserted into the E. coli chromosome and are
consequently replicated with it.
•There are multiple copies of several different insertion sequences (IS elements),
including seven copies of IS2 and five of IS3.
•Both of these IS elements are also found on the F plasmid, and both take part in
the formation of Hfr strains.
•There are several defective integrated viruses that vary from nearly complete virus
genomes to small fragments. Three of these are related to bacteriophage lambda.
12. •E. coli obtained part of its genome by horizontal (lateral) gene transfer from
other organisms.
• Horizontal transfer contrasts with vertical gene transfer in which genes move
from mother cell to daughter cell.
•In fact, it has been estimated that nearly 20% of the E. coli genome originated
from horizontal transfers.
•Horizontally transferred segments of DNA can often be detected because they
have significantly different GC ratios (the ratio of guanine–cytosine base pairs to
adenine–thymine base pairs) or codon distributions from those of the
host organism.
13. •Horizontal gene transfer may cause large-scale changes in a genome.
•For example, strains of E. coli are known that contain virulence genes located on large,
unstable regions of the chromosome called pathogenicity islands that can be acquired
by horizontal transfer.
•Horizontal transfer does not necessarily result in an ever-larger genome size.
•Many genes acquired in this way provide no selective advantage and so are lost by
deletion. This keeps the chromosome of a given species at roughly the same size over
time.
•For example, comparisons of genome sizes of several strains of E. coli have shown
them all to be about 4.5–5.5 Mbp, despite the fact that prokaryotic genomes can vary
from under 0.5 to over 10 Mbp. Genome size is therefore a species-specific trait.
14. Viruses
•Viruses are genetic elements that cannot replicate independently of a living cell
called host cell.
• However, viruses do possess their own genetic information and are thus
independent of the host cell’s genome.
•Viruses rely on the host cell for energy, metabolic intermediates, and protein
synthesis.
•Viruses are therefore obligate intracellular parasites that rely on entering a
suitable living cell to carry out their replication cycle.
15. Viral Genomes
•All cells contain double-stranded DNA genomes. By contrast, viruses have either
DNA or RNA genomes.
•One group of viruses does use both DNA and RNA as their genetic material but at
different stages of their replication cycle.
•Virus genomes can be classified according to whether the nucleic acid in the virion
is DNA or RNA and further subdivided according to whether the nucleic acid is
single- or double-stranded, linear, or circular.
•Some viral genomes are circular, but most are linear.
16.
17. •The nucleic acid of the virion is always located within the particle, surrounded by a
protein shell called the capsid.
•The small genome size of most viruses restricts the number of different viral
proteins that can be encoded. A few viruses have only a single kind of protein in
their capsid, but most viruses have several distinct proteins that are associated in
specific ways to form assemblies called capsomeres.
•The complete complex of nucleic acid and protein
packaged in the virion is called the virus nucleocapsid.
18. The Genome of T-Even Bacteriophages
•Bacteriophages T2, T4, and T6 are closely related, but T4 is the most extensively
studied.
•The genome of T4 is a linear dsDNA molecule of 168,903 base pairs that encodes over
250 different proteins. Although no known virus encodes its own translational
apparatus, T4 does encode several of its own tRNAs. The T4 genome has a unique
linear sequence, but the actual genomic DNA molecules in different virions are not
identical.
•This is because the DNA of phage T4 is circularly permuted. Molecules that are
circularly permuted appear to have been linearized by opening identical circles at
different locations.
•In addition to circular permutation, the DNA in each T4 virion has repeated sequences
of about 3–6 kbp at each end, called terminal repeats. Both of these factors affect
genome packaging.
19.
20. •When T4 DNA enters a host cell, it is first replicated as a unit, and then several
genomic units are recombined end to end to form a long DNA molecule called a
concatemer (Figure 9.13).
•During the packaging of T4 DNA, the DNA is not cut at a specific sequence. Instead,
a segment of DNA long enough to fill a phage head is cut from the concatemer.
•Because the T4 head holds slightly more than a genome length, this “headful
mechanism” leads to circular permutation and terminal redundancy.
•T4 DNA contains the modified base 5-hydroxymethylcytosine in place of cytosine.
These residues are glucosylated, and DNA with this modification is resistant to
virtually all known restriction enzymes. Consequently, the incoming T4 DNA is
protected from host defenses.
21. Retroviruses
•Retroviruses contain an RNA genome that is replicated via a DNA intermediate.
The term retro means “backward,” and the name retrovirus is derived from the
fact that these viruses transfer information from RNA to DNA.
•They were the first viruses shown to cause cancer and have been studied for
their carcinogenic characteristics.
•Also, one retrovirus, human immunodeficiency virus (HIV), causes acquired
immunodeficiency syndrome (AIDS).
22.
23. Features of Retroviral Genomes and Replication
•The genome of the retrovirus is unique. It consists of two identical single-stranded
RNA molecules of the plus ( +) orientation.
•Although there are differences between the genetic maps of different retroviruses, all
contain the following genes arranged in the same order: gag, encoding structural
proteins; pol, encoding reverse transcriptase and integrase; and env, encoding
envelope proteins.
•Some retroviruses, such as Rous sarcoma virus, carry a fourth gene downstream from
env that is active in cellular transformation and cancer. The terminal repeats shown on
the map are essential for viral replication.
24. 1. Entry into the cell by fusion with the
cytoplasmic membrane at sites of specific
receptors
2. Removal of the virion envelope at the
cytoplasmic membrane,
but the genome and virus-specific
enzymes remain in the virus
core
3. Reverse transcription of one of the two
identical genomic RNA molecules into a
ssDNA that is subsequently converted by
reverse transcriptase to a linear dsDNA
molecule, which then enters the nucleus4. Integration of retroviral DNA into the
host genome
5. Transcription of retroviral DNA, leading
to the formation of viral mRNAs and viral
genomic RNA
6. Assembly and packaging of the two
identical genomic RNA molecules into
nucleocapsids in the cytoplasm
7. Budding of enveloped virions at the
cytoplasmic membrane and release from
the cell