- Meiosis is a type of cell division that produces gametes, such as sperm or egg cells, with half the normal number of chromosomes. It involves two rounds of division instead of one, resulting in four daughter cells from one parent cell.
- During meiosis I, homologous chromosome pairs align and separate, reducing the chromosome number by half. Meiosis II is similar to mitosis, where sister chromatids separate to produce four haploid gametes. This ensures genetic variation between offspring and maintains the chromosome number across generations.
This presentation explains the topic of CELL CYCLE and CELL DIVISION.
It includes cell mitosis of both Plant cell and Animal cell with labelled diagrams.
It is the presentation on the MEIOSIS phase of the Cell division.
It includes all the details and definitions that are related to the topic of meiosis with the labelled diagrams.
If you have any query or a question, you may ask in the comment box.
thanks.
This presentation explains the topic of CELL CYCLE and CELL DIVISION.
It includes cell mitosis of both Plant cell and Animal cell with labelled diagrams.
It is the presentation on the MEIOSIS phase of the Cell division.
It includes all the details and definitions that are related to the topic of meiosis with the labelled diagrams.
If you have any query or a question, you may ask in the comment box.
thanks.
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.
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.
The study of the cell cycle focuses on mechanisms that regulate the timing and frequency of DNA duplication and cell division. As a biological concept, the cell cycle is defined as the period between successive divisions of a cell. During this period, the contents of the cell must be accurately replicated.
The cell cycle is regulated by cyclins and cyclin-dependent kinases.
How long is one cell cycle?
Depends. Eg. Skin cells every 24 hours. Some bacteria every 2 hours. Some cells every 3 months. Cancer cells very short. Nerve cells never.
Programmed cell death:
Each cell type will only do so many cell cycles then die. (Apoptosis)
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.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
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.
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.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
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.
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
2. Multicellular organisms grow by the addition
of new cells
New cells arise by the division of pre-existing
cells (Virchow 1858)
Duplication of DNA occur well before cell
division begins
The mode of cell division is fundamentally
similar in all organisms
This shows unity of life
3. A somatic cell exists in two main states
INTERPHASE
A long un-dividing state
MITOTIC PHASE (M PHASE)
A short dividing state
4. The cell grows by synthesizing biological
molecules such as carbohydrates, lipids,
proteins and nucleic acids
It lasts for 10-30 hours
It is divided into 3 periods
First gap phase
G1
Synthetic phase
S
Second gap
G2
5.
6. Gap between previous mitosis and beginning
of DNA synthesis
Carbohydrates, lipids, proteins and RNA are
synthesized
No change occur in the DNA content of the
cell
Muscle and nerve cells never divide again and
remain in G0 phase
7. Duplication of each chromosome by
replication of new DNA molecule
Each chromosome now consists of two
identical sister chromatids
A diploid (2n) cell thus become tetraploid (4n)
Synthesis of histone proteins, mRNAs and
new nucleosomes also occur in this phase
This lasts for 6-8 hours
8. A gap between DNA synthesis and nuclear
division
RNA transcription and protein synthesis
continue
Centrioles, mitochondria and golgi apparatus
are doubled
Proteins for spindle and asters are
synthesized
This lasts for 2-5 hours
9. It is aimed at orderly distribution of the already
duplicated chromosomes to the daughter cells
Many structural and physiological changes occur
in the cell during mitosis
Nuclear envelope breaks down and chromatin is
packed into visible chromosomes
ER and Golgi apparatus breakdown into small
vesicles
Microtubules dissociate into tubulin dimers
Cell activities like gene expression, protein
synthesis, secretion and cell motility, stops
Cell’s entire attention is devoted to the process
of division
11. First described by Robert Remak in RBC of chick
embryo
It occurs without the formation of spindle and
appearance of chromosomes
The nucleus elongates and develops a
constriction round its middle
The constriction gradually deepens and cuts the
nucleus into 2 daughter nuclei
Similar constriction occur in the cytoplasm
between two nuclei and divide the cell into two
12. Amitosis is rare
It occurs in
Mammalian cartilage
Degenerating cells of
diseased tissue
Foetal membranes
13. A common method of cell division in
eukaryotes
Occurs in somatic cells
Lasts for 30 minutes to 3 hours
15. Early prophase
The cell becomes more or less rounded and
cytoplasm turns more viscous
Short radiating microtubules assemble
around centrioles
Two pairs of centrioles of start moving to the
opposite ends of the cell
Microtubules called astral rays are not in
contact with centrioles
16. Between the asters,
long microtubules
assemble on one
sideof the nucleus
called mitotic spindle
Chromosomes first
appear as long thin
thread gradually
change into short thick
rodlets
Chromosomes are fully
replicated at all points
along their lenght
17. Chromosomes finally assume their
characteristics forms and sizes
Nucleoli become smaller and finally
disappear and nucleolar materials are
dispersed into nucleoplasm
Nuclear envelope begins to breakdown into
small vesicles which disperse into cytoplasm
Middle prophase
18. Chromosomes and
other nuclear content
are released into the
cytoplasm
Centriole pairs are
pushed into the
opposite ends of cells
by growing spindles
Spindle and asters are
together called as
mitotic apparatus
Late prophase
19. Lasts for 2-10 minutes
Chromosomes move to
the equatorial plane of
spindle
Chromosomes soon
get aligned at the
middle of the spindle in
the form of plate called
metaphase plate
the Chromosomes are
balanced at the
metaphase plate by
two chromosomal
fibres that connect the
sister kinetochores to
the opposite poles
20. Sister chromatids of each chromosome
slightly separate at the primary constriction
so that their kinetochores stretch towards the
opposite poles of the spindle
Chromosomes are pulled intoV J I shapes
depending upon the position of kinetochores
Anaphase ends when all the chromatids
reach the opposite poles
21. Movement of
chromosomes is called
anaphase A
Extension of poles is
called anaphase B
Chromosomal
microtubules generate
the force for poleward
movements of
chromosomes
22. Long and complex phase lasts for an hour
Chromosomes at each pole unfold and long and
slender
Finally they become undistinguishable as in
interphase cell
Nuclear envelope is reconstructed around each
chromosome
All the envelops fuse to form an envelope
around entire set of chromosomes
Nucleolar material dispersed in the cytoplasm
return to nucleolar organizer and form nucleolus
23. Spindle begin to
disappear by
depolymerisation
of microtubules
Asters become
small till only short
microtubules are
left
Centrioles take up
their characteristic
interphase position
24. Two daughter nuclei formed in telophase are
identical
The accuracy of karyokinesis depends upon
two features
The arrangement of spindle microtubules to
form two distinct poles in the cell
The connection of two chromatids of each
chromosome to the opposite poles of spindle
to ensure their delivery to opposite poles
25. Cell typically divide by a process called
furrowing or cleavage
Short spindle microtubule become structure
less material called mid body
Midbody extends completely across the cell
Then furrow appears in the plasma
membrane at the level of mid body
With the contractile force, furrow gradually
deepens
26. Membranes fuse
Original cytoplasm and
two daughter nuclei
form two independent
daughter cells
New cells are half the
size of mother cells
These enter the G1
phase of next cell cycle
27. It is confined to particular cell and takes place
at a particular time
Cells of sexually reproducing organism
undergo meiosis
It produces gametes in animals and spores in
higher plants
The cells in which meiosis takes place are
called meiocytes (oocytes, spermatocytes,
sporocytes)
28. Meiosis consists of two division that takes
place in the rapid succession with the
chromosomes replicating only once
One parent cell produces four daughter cells
Each having half number of chromosomes
and half amount of nuclear DNA
It is known as reduction division
Two divisions are known as Meiosis I and
Meiosis II
29. It has four phases
Prophase I
Metaphase I
Anaphase I
Telophase I
30. It is more complex than mitotic prophase because of
recombination that occurs in it
It may extents over weeks, months or years
It has five sub-stages
31. Chromosomes appear
as thin thread by
condensation
Each chromosome is
double consisting of
chromatids due to
DNA replication during
interphase
Chromatids are closely
adhere together
32. Homologous
chromosomes come to
lie side by side in pairs
Pairing is called synapsis
A regular space of 0.15to
0.2µm wide exists
between synapsed
homologous
chromosomes
The space have highly
specialized fibriller
organelle synaptonemal
complex
33. Chromatids of synapsed
chromosomes slightly separate
and become visible
Chromosome with two
chromatids called dyad
Group of four homologous
chromatids called tetrads
Two chromatids of same
chromosome is called sister
chromatids
Those of two homologous
chromosomes is called non
sister chromatids
Crossing over occurs in this
stage
It involves mutual exchange of
corresponding segments of non
sister chromatids of
homologous chromosomes
34. Homologous
chromosomes
separate at different
places
This is called
disjunction
Chromosomes do not
separate at certain
points called
chaismata
35. Chromosomes condense again into short
thick rodlets
Centrioles move apart in pairs to the opposite
ends of the cell
Asters form around each centriole
Spindle develop between the centrioles
Nucleolus disintegrate
Nuclear envelope breaks down
Tetrads are released in the cytoplasm
36. Tetrads scattered in the
cytoplasm move to the
equator of spindle
They align in two parallel
metaphase plate
Each homologous
chromosome has two
kinetochores, both are
connected to same spindle
pole
Two kinetochores of a
homologous chromsomes
act as a functional unit in
metaphase-1
38. The nuclear membrane and nucleolus reappear,
cytokinesis follows and this is called as diad of
cells
Although in many cases the chromosomes do
undergo some dispersion, they do not reach the
extremely extended state of the interphase
nucleus.
The stage between the two meiotic divisions is
called interkinesis and is generally short lived.
Interkinesis is followed by prophase II, a much
simpler prophase than prophase I.
39.
40. Prophase II
Meiosis II is initiated immediately after
cytokinesis, usually before the chromosomes
have fully elongated.
In contrast to meiosis I, meiosis II resembles a
normal mitosis.
The nuclear membrane disappears by the end
of prophase II
The chromosomes again become compact.
41. Metaphase II: At this stage the chromosomes align at
the equator and the microtubules from opposite poles
of the spindle get attached to the kinetochores of
sister chromatids
Anaphase II: It begins with the simultaneous splitting
of the centromere of each chromosome (which was
holding the sister chromatids together), allowing
them to move toward opposite poles of the cell
Telophase II: Meiosis ends with telophase II, in which
the two groups of chromosomes once again get
enclosed by a nuclear envelope; cytokinesis follows
resulting in the formation of tetrad of cells that is four
haploid daughter cells
42.
43. Meiosis is the mechanism by which conservation
of specific chromosome number of each species
is achieved across generations in sexually
reproducing organisms, even though the
process, per se, paradoxically, results in
reduction of chromosome number by half. It also
increases the genetic variability in the
population of organisms from one generation to
the next.Variations are very important for the
process of evolution.