This document summarizes the key stages of mitosis and meiosis. It describes that mitosis occurs in somatic cells and results in two identical daughter cells with the same number and type of chromosomes as the parent cell. Meiosis occurs in germ cells and results in four haploid daughter cells each with half the number of chromosomes as the original diploid parent cell. The document outlines the main phases of the cell cycle, including interphase and the phases of mitosis (prophase, metaphase, anaphase, telophase). It also provides details about the key events and phases of meiosis I and meiosis II, including homologous chromosome pairing, crossing over, and the formation of haploid daughter cells.
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)
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)
Introduction to Sexual Reproduction in Flowering Plants, Flower, Structure of Flower, Male Reproductive Part of Flower (Stamens), Development of Anther walls, Anther Walls, Microsporangium (Pollen Sac)
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.
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.
Introduction to Sexual Reproduction in Flowering Plants, Flower, Structure of Flower, Male Reproductive Part of Flower (Stamens), Development of Anther walls, Anther Walls, Microsporangium (Pollen Sac)
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.
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.
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.
(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.
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.
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.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
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.
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 .
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.
1. CELL CYCLE
MITOSIS AND MEIOSIS
DR. DILIP V. HANDE
ASSOCIATE PROFESSOR, DEPT OF BOTANY
SHRI SHIVAJI SCIENCE COLLEGE, AMRAVATI MS.
2. INTRODUCTION:
The number of cells increases by the
division as preexisting cells.
The dividing nucleate cells include two
integral activities i.e. The division of
nucleus (karyokinesis) and division of the
cytoplasm (cytokinesis).
Usually the karyokinesis is followed by the
cytokinesis.
Some times cytokinesis does not follow
karyokinesis these division results in the
formation of multinucleate cells.
3. CELL DIVISION
The cell may divide by any one of the
following methods.
Amitosis or direct cell division
Mitosis or indirect cell division
Meiosis or reduction division
4. AMITOSIS
It is a simple mode of cell division,
generally occurs in unicellular organisms
like bacteria and protozoon.
It this case the nucleus elongate first
become double shaped forming middle
constriction finally form two nuclei and
later on by constriction the cytoplasm the
two daughter cells get formed .
In the process there is complete absence
of nuclear events.
6. MITOSIS
Mitosis generally occurs in somatic (vegetative) cell.
It is the process by which cell divides with sets of
chromosome exactly similar to the parent cell.
Thus number of cells increase without any change in
the genetic composition i.e. structure & number or
chromosome replace and repair of cells in the theory.
The most convenient material for the study of mitosis
is the root tips of onion.
The mitotic cycle or cell cycle includes two distinct
phases.
Inter phase or non dividing period.
Mitotic phase or cell- division period.
7. INTERPHASE :
It is called resting period, but during
this period the cell is metabolically
very active.
In this phase the DNA content is
doubled and also some proteins and
enzymes are synthesized.
Cell prepare itself for the division.
It is longest phase of cell division
include 3 sub- phases.
9. CELL CYCLE
G1 phase (gap period):- It is growth phase
during this synthesis of proteins and RNA
takes place and the cell grows in volume.
S phase :- (synthetic period):- During this
period DNA synthesis occurs i.e replication of
chromosomal DNA takes place which result
in doubling of the chromosomal threads.
G2 (Gap2):- In this part the volume of cell
increases and it is pre division stage, amount
of DNA and cell content becomes more
synthesis of proteins and RNA takes place.
In this phase chromatin fibers are seen.
10. MITOTIC PHASE:
Actual cell division occurs in this phase, it
include karyokinesis and cytokinesis.
Karyokinesis is the division of nucleus into
two daughter nuclei.
It consist of following phases
11. PROPHASE
It is the first phase of
mitosis in which cell
becomes spheroid, and
viscous.
The chromatin material
becomes visible as
separate threads or
chromosomes.
Each chromatid contains a
single DNA molecule.
The two chromatids of a
chromosome are connected
by a centromere.
The nucleolus and nuclear
membrane start
disappearing.
The chromosomes remain
distributed in nucleoplasm.
12. METAPHASE
In this phase the
chromosomes reaches the
central or equatorial
portion of the spindle.
The chromosomes one
lined up in one plane to
form equatorial plate or
metaphasic plate .
There are two kinds of
spindle fibers.
Some fibers are long and
extend from pole to pole.
These are called
continuous fibers.
Other get attached to the
chromosomes at the
centromere these are
called chromosomal fibers.
13. ANAPHASE :
In this phase the centromers of
each chromosome divides into
two.
The two sister chromatids of
each chromosome separate
from each other these
chromatids now called as a
daughter chromosomes.
The two sets of daughter
chromosomes migrate to the
opposite poles of the spindle.
Probably this movement is
caused due shorting of
chromosomal fibers.
Depending to upon the
position of centromere the
chromosomes showing shapes
like V,J,L or I (metacentric
submetacentric and
telocentric).
14. TELOPHASE
This is the last phase in
karyokinesis.
The two sets of daughter
chromosomes reach the opposite
poles.
The chromosomes begin to uncoil
and form chromatin networks.
Nuclear envelope formed around
each set of the chromosomes.
The nucleoli appear at the site of
nuclear organizer.
The after telophase two daughter
nuclei are formed due to
karyokinesis.
Karyokinesis is then followed by
cytokinesis.
15. CYTOKINESIS
The division of cytoplasm into two
daughter cells is called cytokinesis.
It is start simultaneously with telophase
stage.
In plant cells it is accomplished by the
formation of phragmoplast and cell plate.
The tubular elements of E.R. , vesicles of
Golgi complex reach the equator forming
cell plate.
This plate grow and join the cell wall. This
plate later convert into the middle lamella.
16. SIGNIFICANCE OF MITOSIS :-
Mitosis ensures equal distribution of the
nucleus and cytoplasm between the
daughter cells.
The hereditary material (DNA)is also
equally distributed.
The constant number of chromosomes in
all cells of the body is because of mitosis.
Mitosis helps in the growth and
development of the organs and the body
of organisms.
Mitosis help in the repair of damaged
tissues or organs by producing new cells.
Mitosis helps in the asexual reproduction
in some organisms.
17. MEIOSIS
Introduction
The term meiosis was coined by Former in 1905.
It occurs only in the reproductive cells which
results in the formation of haploid gametes.
During meiosis the chromosomes divide once
and the nucleus and cytoplasm divide twice.
Due to this four haploid cells are formed from
diploid cell.
Hence it is also called reduction division.
In this case the haploid daughter cells differ
from each other as well as from mother cell.
18. PROCESS OF MEIOSIS
The process of meiosis shows a sequences of
events similar to those of mitosis but these events
are repeated twice with or without a short
interphase between them.
In the first meiotic division the diploid parent cell
divide into two haploid daughter cells, so this
division is also known as Heterotypic division.
The second meiotic division is a simple mitotic
division.
This division is also known as the homeotypic
division.
Each of the two meiotic cell division is further
distinguished into sub stages.
They are as follows.
19. MEIOSIS-I
It is the first meiotic division during which
the diploid parent cell gives rise to two
haploid daughter cells.
It includes the further phases.
Prophases –I :
This phase has longer duration. It is
having about 5 phases.
20. LEPTOTENE / LEPTONEMA :
In this stage the volume
of the nucleus increases.
Chromosome becomes
uncoiled and long thread
like in shape.
The chromosomes look
beaded in appearance i.e.
each chromosome has
one centromere and
numerous nucleosomes
(beads).
The nucleolus and
nuclear envelop is visible.
21. ZYGOTENE / ZYGONEMA :
In this stage the chromosomes
become shorter and thicker and
pairing of homologous
chromosomes takes place.
The homologous chromosomes
(one paternal and other maternal)
from the two sets are attracted
towards each other and form pairs.
In each pair, the two homologous
lie parallel to each other all along
their lengths.
This pairing is called synapsis and
the paired chromosomes are called
bivalent.
At this stage each chromosome
appear to have only chromatid.
Thus each pair has in all two
chromatids.
Hence each pair is in the dyad
stage.
22. PACHYTENE /
PACHYNEMA
In this stage the
recombination of characters
(genes) takes place through
a phenomenon called
crossing over.
The chromosome becomes
shorter, thicker, distinct now
each chromosome has two
sister chromatids joined by
a centromere.
Thus each pair of the
homologous chromosomes
(bivalent ) at this stage
consist of four chromatids (
23. PACHYTENE / PACHYNEMA
The non sister chromatids are twisted round
each other and may take part in crossing
over.
The chromatid is the unit of crossing over.
Two chromatid belonging to two different
homologues (non- sister chromatids)
undergo one or more breaks at the same
level.
After the break inter change of chromatid
segments takes place between the non-
sister chromatids.
The broken chromatid segments unit with
other chromatids due to presence of an
enzyme ligase.
This process inter change of chromatin
24. D) DIPLOTENE/ DIPLONEMA :
In this stage the homologous chromosomes
repel each other as the force of attraction
between them decreases.
The separating chromosomes are held
together at one or more points, where
crossing over occurred.
These points are called chiasmata. The
number of chiasmata varies with the
length of the chromosomes.
Generally shorter chromosomes have few
chiasmata than the longer ones.
By the end of diplotene, the chiasmata
begin to move from the centromere
towards the end.
This displacement of chiasmata is termed
as terminalization.
When terminalization is complete the
homologous chromosomes are held
together by the terminal chiasmata.