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Helloo!!! everyone, I'm student of M.Sc. Microbiology at Parul University, and i've made this presentation on "The Cell Cycle" focusing more on 'Mitosis and Meiosis'.
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The cell cycle, or cell-division cycle, is the series of events that take place in a cell that cause it to divide into two daughter cells. These events include the duplication of its DNA (DNA replication) and some of its organelles, and subsequently the partitioning of its cytoplasm and other components into two daughter cells in a process called cell division.
here u will find every detail of cell cycle.
for more details ,visit @biOlOgy BINGE-insight learning
this presentation has detailed information on cell cycle. it includes steps as well as how the proteins take part in cell cycle.
i have also added information on some experiments that were carried out.
happy studying :)
a deeply explained process of cell division, for understanding it thoroughly. i tried to put in all the information i knew and collected. i hope it is helpful or you.
The cell cycle, or cell-division cycle, is the series of events that take place in a cell that cause it to divide into two daughter cells. These events include the duplication of its DNA (DNA replication) and some of its organelles, and subsequently the partitioning of its cytoplasm and other components into two daughter cells in a process called cell division.
here u will find every detail of cell cycle.
for more details ,visit @biOlOgy BINGE-insight learning
this presentation has detailed information on cell cycle. it includes steps as well as how the proteins take part in cell cycle.
i have also added information on some experiments that were carried out.
happy studying :)
a deeply explained process of cell division, for understanding it thoroughly. i tried to put in all the information i knew and collected. i hope it is helpful or you.
The sequence of events cell division, DNA replication and cell growth by which a cell duplicates its genome, eventually divides into two daughter cells is termed cell cycle.
OVERVIEW OF CELL CYCLE
Explained in brief phases of cell cycle . Given a explanation of each phase in detail, also explained the significance of meiosis in brief.
Cell division is a process by which cell reproduce itself and divides into two or more daughter cells. The cell cycle is defined as the period between successive divisions of a cell. It is an orderly sequence of events by which a somatic cell duplicates its contents and divides in two.
This presentation include the process of cell division. It hope it will helpful for all the medical students. Cell division is the series of events of equally dividing of one single mother cell into two identical daughter cell. Cell cycle and cell division terms are alternately used. Cell division is an important part of the all living processes.
At the time of cell division, RNA replication is a natural process.
The cell cycle, or cell-division cycle, is the series of events that take place in a cell that cause it to divide into two daughter cells.
These events include the duplication of its DNA (DNA replication) and some of its organelles, and subsequently the partitioning of its cytoplasm and other components into two daughter cells in a process called cell division.
There are two types of cell division
A) Mitosis and Binary fission – (Asexual reproduction) and B) Meiosis – (Sexual reproduction)
In prokaryotic cell, the cell division occurs via a process termed as Binary fission.
• In eukaryotic cell, the cell cycle can be divided in two periods i.e Interphase and Mitosis.
• During Interphase, the cell grows and DNA is replicated.
During Mitotic phase, the replicated DNA and cytoplasmic contents are separated, and cell divides.
The duration of cycle varies from hours to years. A typical human cell cycle has duration of 24 hours.
Some cells, such as skin cells, are constantly going through cell cycle, while other cells may divide rarely.
Some cells don’t grow and divide once they mature for ex. Neuron
Eukaryotic cell have a more complex cell cycle than prokaryotic cell.
The cell cycle, or cell-division cycle, is the series of events that take place in a cell leading to duplication of its DNA (DNA replication) and division of cytoplasm and organelles to produce two daughter cells.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
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.
Richard's entangled aventures in wonderlandRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
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.
A brief information about the SCOP protein database used in bioinformatics.
The Structural Classification of Proteins (SCOP) database is a comprehensive and authoritative resource for the structural and evolutionary relationships of proteins. It provides a detailed and curated classification of protein structures, grouping them into families, superfamilies, and folds based on their structural and sequence similarities.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
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What is greenhouse gasses and how many gasses are there to affect the Earth.moosaasad1975
What are greenhouse gasses how they affect the earth and its environment what is the future of the environment and earth how the weather and the climate effects.
2. The_Cell_Cycle_Shiven_Trambadia
The Cell Cycle
● The cell cycle is an ordered series of events. It is the sequence of events by
which a cell duplicates its genome and eventually divides into two daughter
cells.
● The cell cycle has two main phases - interphase and M-phase.
● The period of actual division, corresponding to the visible mitosis, is called M
phase (mitosis phase).
● The Interphase is the time during which the cell is preparing for division by
undergoing both cell growth and DNA replication in an orderly manner.
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3. The_Cell_Cycle_Shiven_Trambadia
● The interphase is further subdivided into;
○ G1 phase (Gap 1, the period between the end of M phase and the start of DNA replication);
○ S phase (Synthesis, the period during which DNA synthesis occurs); and
○ G2 phase (Gap 2, the gap period following DNA replication and preceding the initiation of the
M phase)
● Cells that do not divide enter into G0 state. Most cells in our body are in G0
state.
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4. The_Cell_Cycle_Shiven_Trambadia
Mitosis
● Mitosis was firstly introduced by Walther Flemming in 1882.
● Mitosis partitions newly replicated chromosomes equally into two daughter
cells.
● Mitosis leads to one round of DNA replication followed by one round of
Chromosome segregation and giving rise to two genetically identical daughter
cells.
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5. The_Cell_Cycle_Shiven_Trambadia
Stages of M-phase
● The M-phase starts with karyokinesis (nuclear division), forming two
daughter nuclei and generally ends up with cytokinesis (cytoplasm division).
● Conventionally mitosis is divided into 4 substages: prophase, metaphase,
anaphase and telophase.
● Cells show different physical characteristics when reaching in each of these
phases.
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7. The_Cell_Cycle_Shiven_Trambadia
Prophase
● The diffuse chromatin in interphase, now slowly starts to condense during
the beginning of prophase.
● Chromosomes are duplicated during the previous S-phase and consists of
two sister chromatids, which are held together at a constricted region
called, Centromere.
● At centromere, sister chromatids are held together by a membrane of the
SMC (Structural Maintenance of Chromosomes), included in the family of
proteins, called cohesin.
● At the end of prophase, cytoplasmic microtubules disassemble and starts the
formation of mitotic spindle.
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8. The_Cell_Cycle_Shiven_Trambadia
Prophase
● At the end of prophase nucleolus disappears along with the nuclear envelope.
● Most of the cells mark the end of the prophase when nuclear envelope
disrupts. But, nuclear envelope disruption is not universally observed feature
of mitosis. Eg; Yeast cells don’t loose nuclear envelope during cell division.
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9. The_Cell_Cycle_Shiven_Trambadia
Metaphase
● Metaphase is an very dynamic part of the cell cycle.
● Spindle fibres rapidly assemble and disassemble as
they grow out of the Microtubule Organizing
Center (MTOC), seeking out attachment sites at
chromosome.
● For attachment of spindle fibres, each chromosome
has a special structure called kinetochore.
● There are two kinetochores located at the
centromere, on each chromosome facing in opposite
directions.
● Chromosomes are now lined up to the Equator of
the cell.
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10. The_Cell_Cycle_Shiven_Trambadia
Anaphase
● The kinetochore microtubules pull the
two kinetochores towards the opposite
poles, at anaphase.
● The cohesins holding together the two
sister chromatids, are now digested by
another protein, Separase.
● Until anaphase the separase is kept in
active form by another protein, Securin.
● After separation, each chromatid, which
are now called as chromosome, are
pulled towards the polls they face,
opposite to each other. 10
11. The_Cell_Cycle_Shiven_Trambadia
Telophase
● Separated daughter chromosomes
arrive at the poles and the
kinetochore microtubules
disappears, at Telophase.
● Still polar microtubule elongates
more, and a new nuclear
envelope re-forms around each
set of daughter chromosomes.
● Condensed chromatin expands
again and the nucleoli reappears,
marking the end of the mitosis.
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12. The_Cell_Cycle_Shiven_Trambadia
Cytokinesis
● Division of cytoplasm after karyokinesis is referred as cytokinesis.
● Cytokinesis begins in anaphase and ends in telophase.
● Mechanism of cytokinesis in animals and plants cell vary, in former it is
completed by cleavage and in latter by cell plate formation.
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13. The_Cell_Cycle_Shiven_Trambadia
Meiosis
● Farmer and Moore, explained that a specialized cell division in which number
of chromosomes is reduced to half is
● This reduction in chromosome number is achieved by one round of DNA
replication, followed by two rounds of chromosome segregation with no
intervening rounds of DNA replication.
● Meiosis is divided into two parts, meiosis I and meiosis II. At the end of
meiotic process, there are four daughter cells, each having half the total
number of chromosomes as parent cell.
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15. The_Cell_Cycle_Shiven_Trambadia
Meiosis 1
● Prophase 1 of meiosis 1 is divided into five sub-stages: Leptotene,
Zygotene, Pachytene, Diplotene and Diakinesis.
● Leptotene: although each chromosome has replicated and consists of two
sister chromatids, these chromatids are unusually closely apposed, and each
chromosome therefore appears to be single.
● In leptotene to zygotene transition, the tips of the chromosomes move until
most end up in a limited region near each other, this arrangement is called a
Bouquet stage.
● It facilitates homologous chromosome pairing and synapsis.
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16. The_Cell_Cycle_Shiven_Trambadia
Zygotene
● As soon as the intimate pairing, between the two homologs initiates it marks
the starting of Zygotene.
● Synapsis often starts when the homologous end of the two chromosomes are
brought together on the nuclear envelope and proceeds inward in a zipper
fashion from both ends.
● Each pair of homologous chromosomes forms as a result of synapsis is called
a bivalent.
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17. The_Cell_Cycle_Shiven_Trambadia
Pachytene
● As soon as the synapsis is completed all along the chromosomes, the cells
are said to have entered the pachytene stage.
● The paired chromosomes now get shorten and thicken.
● At this stage , large recombination nodules appear at the intervals on the
synaptonemal complexes.
● Crossing over is a reciprocal exchange of equal and corresponding segment
between non-sister chromatids in a pair of homologous chromosome.
● It leads to the recombination of genes present on two homologous
chromosomes.
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18. The_Cell_Cycle_Shiven_Trambadia
Diplotene
● Desynapsis begins in the diplotene stage of meiotic prophase 1.
● Synaptonemal complex dissolves, allowing the two homologous
chromosomes in a bivalent to pull away from each other to some extent.
● But, each bivalent remains attached by one or more chiasmata.
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19. The_Cell_Cycle_Shiven_Trambadia
Diakinesis
● Diplotene merges imperceptibly into diakinesis, the stage of transition to
metaphase, as RNA synthesis ceases and the chromosomes condense,
thicken and become detached from the nuclear envelope.
● Now each bivalent consists of four separate chromatids, with each pair of
sister chromatids linked at their centromeres.
● Now cell enters Metaphase 1.
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21. The_Cell_Cycle_Shiven_Trambadia
Metaphase 1
● Breakdown of nuclear membrane and attachment of kinetochore microtubules
to bivalent, marks the initiation of Metaphase 1.
● Homologous pairs move together along the metaphase plate.
● Independent assortment is based on the physical orientation of chromosomes
of each bivalent along the metaphase plate, with respect to that of other
bivalents along the same equatorial line.
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23. The_Cell_Cycle_Shiven_Trambadia
Anaphase 1
● Homologous chromosomes are separated in Anaphase 1.
● Sister chromatids stay together.
● Special meiosis specific cohesin, Rec8 inhibits the separation of sister
chromatids.
● Homologous chromosomes separate and move to opposite poles. The
meiotic division is hence, called the reductional division, as it reduces the
chromosome number to half the diploid number in each daughter cell.
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24. The_Cell_Cycle_Shiven_Trambadia
Telophase 1
● As soon as the chromosomes arrive at the
poles meiosis 1 is said to have been ended
effectively.
● Now each daughter cell has half the number
of chromosomes left, with a pair of
chromatids.
● New nuclear membrane surrounds each
haploid set.
● Chromosomes are uncoiled back to
chromatin.
● Cytokinesis take place, generating two
daughter cells. 24
25. The_Cell_Cycle_Shiven_Trambadia
Meiosis 2
● Time gap between Meiosis 1 and Meiosis 2 is called interkinesis.
● It is usually short or may not occur at all, at this stage no DNA replication
occurs.
● Meiosis 2 is similar to that of Mitosis.
● But, no S phase occurs during Meiosis 2.
● Now the chromatids of each chromosome are not identical due to
recombination taken place in prophase 1 of meiosis 1.
● Meiosis 2 separates the sister chromatids producing two daughter cells each
with a haploid chromosome number.
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