Cell division is a very important process in all living organisms. During the division of a cell, DNA replication and cell growth also take place. All these processes, i.e., cell division, DNA replication, and cell growth, hence, have to take place in a coordinated way to ensure correct division and formation of progeny cells containing intact genomes.
In eukaryotes, there are two distinct types of cell division: a vegetative division, whereby each daughter cell is genetically identical to the parent cell (mitosis), and a reproductive cell division, whereby the number of chromosomes in the daughter cells is reduced by half to produce haploid gametes (meiosis).
This PowerPoint, designed by East Stroudsburg University student Kristen O'Connor, is a PowerPoint designed for middle school science students on cell organelles.
This PowerPoint, designed by East Stroudsburg University student Kristen O'Connor, is a PowerPoint designed for middle school science students on cell organelles.
This presentation is about how cell cycle and cell division takes place in plant and animal cell .... and this presentation also includes mitosis and meiosis and significance of it.
Cell biology
Want to know the difference between Centrioles and Centrosome?
Check this ppt to know more about it!
-- Importance of these cellular organelles in a life.
-- Disorders related to these organelles.
-- Recent advancements in the field of Cancer and Cell biology.
By Mohammed Valikarimwala
SY BSc Biotechnology
Fergusson college, Pune.
Multicellular organisms develop from a single cell known as zygote by the process of mitosis. Asexual reproduction in some organisms like amoeba and vegetative reproduction in plants takes place by mitosis. This type of cell division involves many steps and it does not alter the genetic material.
This presentation is about how cell cycle and cell division takes place in plant and animal cell .... and this presentation also includes mitosis and meiosis and significance of it.
Cell biology
Want to know the difference between Centrioles and Centrosome?
Check this ppt to know more about it!
-- Importance of these cellular organelles in a life.
-- Disorders related to these organelles.
-- Recent advancements in the field of Cancer and Cell biology.
By Mohammed Valikarimwala
SY BSc Biotechnology
Fergusson college, Pune.
Multicellular organisms develop from a single cell known as zygote by the process of mitosis. Asexual reproduction in some organisms like amoeba and vegetative reproduction in plants takes place by mitosis. This type of cell division involves many steps and it does not alter the genetic material.
It discuss about cell division in prokaryotes, eukaryotes. It also discuss on meiotic division starts from interphase, prophase I, Metaphase I, Anaphase I & telophase I and also Prophase II, Metaphase II, Anaphase II, Telophase II and conclusion
Dr. Smita Lande Department of Botany, Late Pundalikrao Gawali Arts and Science Mahavidyalaya, Shirpur (Jain). Presentation for B.Sc. II sem IV students
CELL DIVISION- Decoding Cell Division: The Dance of Life's ContinuityNursing Mastery
Decoding Cell Division: The Dance of Life's Continuity
Step into the mesmerizing world of cell division with our illuminating SlideShare presentation. From the elegant choreography of mitosis to the intricacies of meiosis, witness the remarkable processes that underpin life's continuity and diversity.
In this captivating presentation, we delve deep into the mechanisms of cell division, unraveling the stages and significance of mitosis and meiosis. Explore how cells meticulously replicate their DNA, segregate their chromosomes, and orchestrate their division to ensure the transmission of genetic information with precision and fidelity.
Through vivid illustrations, clear explanations, and real-world examples, we illuminate the significance of cell division in growth, development, and reproduction. Gain a newfound understanding of how errors in cell division can lead to diseases like cancer and genetic disorders, and learn about the cutting-edge research driving advancements in this field.
Whether you're a student, educator, or enthusiast of life sciences, our presentation offers valuable insights into one of the most fundamental processes of life. Join us as we unravel the mysteries of cell division and marvel at the beauty and complexity of nature's continuity.
Don't miss this opportunity to deepen your knowledge and appreciation of cell biology. Embark on a journey into the heart of cell division and discover the dance of life's continuity unfolding before your eyes.
(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 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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Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
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.
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...University of Maribor
Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Track: Artificial Intelligence
https://www.etran.rs/2024/en/home-english/
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
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.
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.
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.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...
@ cell cycle - mitosis and meiosis (mnusratgulbarga@gmail.com)
1. MSc, Department of Bioinformatics, KSAWU, Vijayapura 1
Karnataka State Women's University VIJAPUR
SUBJECT : CELL AND MOLECULAR BIOLOGY
SUBJECT CODE : BI. HCT 1.1
2. 1. Cell Division – Introduction
2. Prokaryotes - Cell Division
3. Eukaryotes - Cell Division
A. Mitosis
B. Meiosis
4. Differences Between Mitosis
And Meiosis
3. All cells are derived from pre-existing cells.
New cells are produced for growth and to replace damaged
or old cells.
Cell division differ in prokaryotes (bacteria ) and eukaryotes
( protista, fungi, plants and animals).
Before a cell becomes too large, it divides, producing 2 or 4
daughter cells.
Before the cell divides, the DNA is replicated, so each new
cell will have the same genetic information as the parent cell.
1655 – Hooke described ‘cells’ in cork.
INTRODUCTION
MSc, Department of Bioinformatics, KSAWU, Vijayapura 3
4. Prokaryotes have no nucleus.
They have a single circular chromosome.
Prokaryotes simply divide their cells in two by binary
fission , where their genetic material is segregated
equally into two daughter cells.
There are alternative manners of division, such as
budding, that have been observed.
MSc, Department of Bioinformatics, KSAWU, Vijayapura 4
5. Prokaryotes such as bacteria
divide into 2 identical cells by
the process of binary fission
Single chromosome makes a
copy of itself .
Cell wall forms between the
chromosomes dividing the cell .
MSc, Department of Bioinformatics, KSAWU, Vijayapura
5
6. Eukaryotes
In eukaryotes, there are two distinct types of cell
division:
A vegetative division, whereby each daughter cell is
genetically identical to the parent cell (mitosis).
A reproductive cell division, whereby the number of
chromosomes in the daughter cells is reduced by half to
produce haploid gametes (meiosis).
MSc, Department of Bioinformatics, KSAWU, Vijayapura
6
7. The sequence of events by which a cell duplicates
its genome, synthesizes the other constituents of
the cell and eventually divides into two daughter
cells is termed as cell cycles.
MSc, Department of Bioinformatics, KSAWU, Vijayapura 7
8. G1 – primary growth phase
S- synthesis; DNA replicated
G2 – secondary growth phase
collectively theses 3 stages are called interphase
M – mitosis
c- cytokinesis
90%
10%
MSc, Department of Bioinformatics, KSAWU, Vijayapura
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9. Interphase – G1 phase
Growth of cell
Duplication of organelles
Synthesis of proteins
Interphase – S phase
DNA synthesis occurs.
DNA replication begins in the
nucleus.
The centriole duplicates in the
cytoplasm.MSc, Department of Bioinformatics,
KSAWU, Vijayapura
9
10. 2nd Growth Stage
Occurs after DNA has been duplicated or replicated
All cell organelles & proteins needed for division are
synthesized
Interphase – G 2 phase
MSc, Department of Bioinformatics,
KSAWU, Vijayapura
10
11. Includes 2 parts :
1. Mitosis
PROPHASE
PROMATAPHASE
METAPHASE
ANAPHASE
TELOPHASE
2. Cytokinesis
M phase
MSc, Department of Bioinformatics,
KSAWU, Vijayapura
11
12. Mitosis is a process of cell division in which chromosome
replicates and get equally distributed into two daughter
cells so that these cells have the same number and type of
chromosome as present in the parent cell.
Mitosis
In 1835, German botanist
Hugo von Mohl
discovered mitosis in cells of
algae Cladophora glomerata.
MSc, Department of Bioinformatics, KSAWU, Vijayapura
12
13. Duration : 15 minutes
Chromosome condenses and coil, they become
visible under light microscope.
The two sister chromatids of each chromosome
attach at a point called centromere.
Spindle fibers begin to form from two centrosome,
and they will start moving apart .
PROPHASE
PROMETAPHASE
Duration : 15 minutes
The nuclear membrane disappears.
Kinetochore will get attached to the centromere
The spindle fibers become attached to the
kinetochore
MSc, Department of Bioinformatics, KSAWU, Vijayapura
13
14. Duration : 20 minutes
Spindle fibres attach to kinetochores of
chromosomes.
Chromosomes are moved to equator and get aligned
along metaphase plate through spindle fibers get
seperated to both poles.
METAPHASE
ANAPHASE
Duration: 3 minutes
Sister chromatids are pulled apart to
opposite poles of the cell by kinetochore
fibers
MSc, Department of Bioinformatics,
KSAWU, Vijayapura
14
15. TELOPHASE
Duration : 10 minutes
Chromosomes cluster at opposite
spindle poles and their identity is
lost as discrete elements.
Nuclear envelope assembles around
the chromosome clusters.
Nucleolus, Golgi complex and ER
reform.
MSc, Department of Bioinformatics, KSAWU, Vijayapura
15
16. Cytokinesis is the division of the
cytoplasm
Results in two separate daughter cells
with identical nuclei
Occurs at the same time as telophase
CYTOKINESIS
Animal cells Plant cells
Cell membrane is drawn
inward until the
cytoplasm is pinched
into 2 nearly equal parts
Cell plate forms
midway between
the divided nuclei
Cell wall begins to
appear in the cell
plate.MSc, Department of Bioinformatics,
KSAWU, Vijayapura
16
20. In 1882, British cytologist
Pierre-Joseph van Beneden
he observed that gametes (sperm &
egg) contain half the number of
chromosomes compared to somatic
cells(non reproductive cells).
MEIOSIS
Meiosis - the process of cell division that produces
haploid gametes (half the number of chromosomes:
humans: 23)
MSc, Department of Bioinformatics, KSAWU, Vijayapura
20
21. Reduction Division
• Cell undergoes 2 rounds of cell
division:
•Meiosis 1
•Meiosis 2
MSc, Department of Bioinformatics, KSAWU, Vijayapura
21
22. Meiosis I
• Preceded by Interphase- chromosomes are replicated
to form sister chromatids
• Sister chromatids are genetically identical and joined
at centromere
• Single centrosome replicates, forming 2 centrosomes
MSc, Department of Bioinformatics, KSAWU, Vijayapura
22
23. Prophase I
• Individual chromosomes first become visible
– homologous chromosomes become closely
associated in synapsis
– crossing over occurs
MSc, Department of Bioinformatics, KSAWU, Vijayapura
23
24. Metaphase I
• The homologous chromosomes line up in the equator
of the cell and are still held together
MSc, Department of Bioinformatics, KSAWU, Vijayapura 24F
25. Anaphase I
• Spindle fibers shorten
• The homologous chromosomes are separated (the
sister chromatids are still paired)
MSc, Department of Bioinformatics, KSAWU, Vijayapura
25
26. Telophase I
• The nuclear membrane reforms around each
daughter nucleus
• Each new cell now contains two sister chromatids
that are NOT identical due to crossing over
MSc, Department of Bioinformatics, KSAWU, Vijayapura
26
27. At the end of Meiosis I…
• At the end we have 2 cells
• Each cell contains a haploid number of
chromosomes – 1 copy of each chromosome (for
humans, each haploid cell has 23 chromosomes)
• No DNA replication occurs between Meiosis I
and Meiosis II
MSc, Department of Bioinformatics, KSAWU, Vijayapura
27
28. Prophase II
• Nuclear membrane breaks down again
MSc, Department of Bioinformatics, KSAWU, Vijayapura
28
29. Metaphase II
• The chromosomes line up in the middle of
the cell.
MSc, Department of Bioinformatics, KSAWU, Vijayapura
29
30. Anaphase II
• The spindle fibers shorten and the sister
chromatids move to opposite poles.
MSc, Department of Bioinformatics, KSAWU, Vijayapura
30
31. Telophase II
• Nuclear envelope re-forms around the four
sets of daughter chromosomes.
MSc, Department of Bioinformatics, KSAWU, Vijayapura
31
32. At the end of Meiosis II…
• At the end of Meiosis II, there are 4
haploid cells.
• No two of these haploid cells are alike due
to crossing over.
MSc, Department of Bioinformatics, KSAWU, Vijayapura
32
33. Comparison of Divisions
Mitosis Meiosis
Number of
divisions
1
2
Number of
daughter cells
2 4
Genetically
identical?
Yes No
Chromosome # Same as parent Half of parent
Where Somatic cells Germ cells
When Throughout life At sexual maturity
Role Growth and repair Sexual reproduction
MSc, Department of Bioinformatics, KSAWU, Vijayapura
33
34. Reference
MSc, Department of Bioinformatics, KSAWU, Vijayapura
34
1. ^ Cells : building blocks of life. Maton, Anthea. (3rd ed.). Upper Saddle
River, N.J.: Prentice-Hall. 1997. pp. 70–74. ISBN 978-0134234762.
OCLC 37049921.
2. ^ Cell division : theory, variants, and degradation. Golitsin, Yuri N.,
Krylov, Mikhail C. New York: Nova Science Publishers. 2010. p. 137.
ISBN 9781611225938. OCLC 669515286.
3. ^ Molecular cell biology 5th edition LODISH . BREK . BREAK .
MATSUDAIRA. KAISER. KRIEGER. SCOTT. ZIPURSKY. DARNELL.