Chromosomes carry genes in a linear sequence that is shared by members of a species. In prokaryotes, DNA exists as a single circular chromosome, while eukaryotes have multiple linear chromosomes associated with histone proteins. Homologous chromosomes in diploid cells contain the same genes but can have different alleles. Sex is determined by X and Y chromosomes in most species. Karyotyping allows visualization of chromosomes and can be used for analysis.
A work in progress - drafts to be updated and completed later. Practice with the the assessment statements from the Core component of the course that require diagrams.
A Powerpoint for Grade 12 Life Sciences / Biology students focussing on chromosomes and meiosis. Contains information and diagrams on meiosis, mitosis, the structure of chromosomes, DNA and RNA
The Greek words "Chroma," which means colour, and "Soma," which means body, were combined to create the English word "chromosome." They are distinct cell organelles made of chromatin, the most significant and durable component of the cell nucleus. They have the ability to reproduce themselves. They are important for differentiation, heredity, mutation, and evolution and regulate the structure and metabolism of cells.
General History of Chromosomes
Nuclear filaments were found by W. Hofmeister in the Tradescantia pollen mother cells' nuclei in 1848. W. Flemming conducted the first precise chromosome count in a cell's nucleus in 1882. W. Flemming, Evan Beneden, and E. Strasburger showed in 1884 that the chromosomes double in number during mitosis through longitudinal division. Beneden discovered that each species had a fixed number of chromosomes in 1887. W. Waldeyer first used the term "chromosomes" for the nuclear filaments in 1888. The role of chromosomes in heredity was first proposed by W.S. Sutton and T. Boveri in 1902, and it was later supported by Morgan in 1933.
In viruses, prokaryotes, and eukaryotes, chromosome structures differ.
1. Viral chromosome- In viruses, each chromosome contains a single nucleic acid molecule (DNA or RNA), which is encased in a protein coat known as the capsid. It could be circular or linear. The term "DNA virus" refers to viruses with DNA as their genetic material, while the term "RNA virus" refers to viruses with RNA as their genetic material. The viral chromosome contains a small amount of genetic material that primarily regulates the generation of additional identical virus particles in the host cell. In RNA viruses, the RNA frequently instructs the host's reverse transcription process to create DNA that is complementary to itself.
The DNA then uses the RNA to create new viral particles by transcribing it. Retroviruses are one type of ribovirus. A retrovirus is what causes AIDS.
2. Prokaryotic chromosomes- A single circular two-stranded DNA molecule found on prokaryotic chromosomes, such as those found in bacteria, is not encased by any membrane. It is in direct contact with the cytoplasm and is protein-free.
Some RNA that seems to form a core encases the bacterial chromosome in the nucleoid. At some point, it is anchored permanently to the plasma membrane. Most bacterial cells also contain some extra-chromosomal DNA molecules that are double stranded and circular but much smaller in size than the main chromosome. Plasmids are the name for them.
The plasmid can appear on its own in the cytoplasm of cells or it can also be discovered in associated with the main chromosomal DNA and is known as an episome.
3. Eukaryotic chromosomes- The nucleus and some other organelles, like mitochondria and plastids, contain the eukaryotic chromosomes. Nuclear and extra nuclear chromosomes are the names given to these chromosomes, respectively.
Double-stranded, linear, long DNA molecules make up nuclear chromosomes. They are
A chromosome is a long DNA molecule with part or all of the genetic material of an organism. Most eukaryotic chromosomes include packaging proteins called histones which, aided by chaperone proteins, bind to and condense the DNA molecule to maintain its integrity.
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.
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.
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
Thanks...!
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 .
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.
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.
1. 3.2 Chromosomes
Essential
Question:
Chromosomes
carry genes in
a linear
sequence that
is shared by
members of a
species.
http://41.media.tumblr.com/4c08ea6
94bcf30c5a9d8423187fba2de/tumblr
_mx5zd49kWN1qjofuoo1_1280.jpg
Stages of Mitosis by Walter Flemming January 1882
2. Understandings
Statement Guidance
3.2.U1 Prokaryotes have one chromosome consisting of a circular DNA molecule.
3.2.U2 Some prokaryotes also have plasmids but eukaryotes do not.
3.2.U3 Eukaryote chromosomes are linear DNA molecules associated with histone proteins.
3.2.U4 In a eukaryote species there are different chromosomes that carry different genes.
3.2.U5
Homologous chromosomes carry the same sequence of genes but not necessarily the same alleles of those
genes.
3.2 U6 Diploid nuclei have pairs of homologous chromosomes.
3.2 U7
Haploid nuclei have one chromosome of each pair. [The two DNA molecules formed by DNA replication prior
to cell division are considered to be sister chromatids until the splitting of the centromere at the start of
anaphase. After this, they are individual chromosomes.]
3.2 U8 The number of chromosomes is a characteristic feature of members of a species.
3.2 U9
A karyogram shows the chromosomes of an organism in homologous pairs of decreasing length. [The terms
karyotype and karyogram have different meanings. Karyotype is a property of a cell—the number and type
of chromosomes present in the nucleus, not a photograph or diagram of them.]
3.2 U10 Sex is determined by sex chromosomes and autosomes are chromosomes that do not determine sex.
3. Applications and Skills
Statement Guidance
3.2 A1 Cairns’ technique for measuring the length of DNA molecules by autoradiography.
3.2 A2
Comparison of genome size in T2 phage, Escherichia coli, Drosophila melanogaster, Homo sapiens and Paris
japonica. [Genome size is the total length of DNA in an organism. The examples of genome and chromosome
number have been selected to allow points of interest to be raised
3.2 A3
Comparison of diploid chromosome numbers of Homo sapiens, Pan troglodytes, Canis familiaris, Oryza
sativa, Parascaris equorum.
3.2 A4 Use of karyograms to deduce sex and diagnose Down syndrome in humans.
3.2 S1 Use of databases to identify the locus of a human gene and its polypeptide product.
4. 3.2 U1 Prokaryotes have one chromosome consisting of a
circular DNA molecule.
• Prokaryotic DNA is
circular and is not
associated with any
histone proteins
• There is one copy of
each gene except
when the cell and its
DNA are replicating
Bacterial
DNA
Plasmids
5. 3.2 U1 Prokaryotes have one chromosome consisting of a
circular DNA molecule.
https://classconnection.s3.amazonaws.com/730/flashcards/127
6730/jpg/cell_types1330806303645.jpg
6. 3.2 U.2 Some prokaryotes also have plasmids but eukaryotes
do not.
http://upload.wikimedia.org/wikipedia/en/6/6c/PBR322_pl
asmid_showing_restriction_sites_and_resistance_genes.jpg
• Plasmids are small separate (usually
circular) DNA molecules located in
some prokaryotic cells
• Plasmids are also naked (not
associated with proteins) and are not
needed for daily life processes in the
cell.
• The genes in plasmids are often
associated with antibiotic resistant
and can be transferred from one
bacterial cell to another.
• Plasmids are readily used by scientists
to artificially transfer genes from one
species to another (ie. Gene for
human insulin)
7. Nucleosome Structure: consist of 8 histones. They help create super coiling of
chromatin, which creates a chromosome during cell replication
3.2 U.3 Eukaryote chromosomes are linear DNA molecules associated with histone proteins.
http://micro.magnet.fsu.edu/cells/nucleus/images/
chromatinstructurefigure1.jpg
8. • Eukaryotic chromosomes are linear
and are made up of DNA and
histone proteins.
• Histones are globular shaped
protein in which the DNA is
wrapped around.
• DNA wrapped around 8 histone
proteins is called a nucleosome.
• The DNA wraps twice around the
histone protein core.
• Another histone protein is attached
to the outside of the DNA strand.
This helps maintain the colloidal
structure of the nucleosome.
• DNA, because of its negative charge
is attracted to the positive charge
on the amino acids of the histone
proteins.
3.2 U.3 Eukaryote chromosomes are linear DNA molecules
associated with histone proteins.
http://upload.wikimedia.org/wikipedia/commons/
4/45/Nucleosome_organization.png
9. 3.2 U4 In a eukaryote species there are different chromosomes
that carry different genes.
https://s-media-cache-
ak0.pinimg.com/originals/4d/d0/7
a/4dd07a61c384abefef3c521bcab
6bad8.jpg
http://dxline.info/img/new_ail/chro
mosome-4.jpg
• Chromosomes are
linear, varying in length
and in position of the
centromere that holds
the sister chromatids
together.
• In humans there are 23
types of chromosomes.
Each chromosome
carries a specific
sequence of genes
along the linear DNA
molecule. The position
where the gene is
located is called the
locus.
Chromosome 1 Chromosome 4
2,000 Genes 1,000 Genes
10. 3.2 U.5 Homologous chromosomes carry the same sequence
of genes but not necessarily the same alleles of those genes.
https://molecularhelix.files.wordpress.com/2011/07/homolg.gif
• Homologous chromosomes
are chromosomes within each
cell that carry the same genes
• One chromosome came from
an individual’s mother and
one from the father
• They have the same shape
and size
• These chromosomes pair up
during meiosis
• Even though these
chromosomes carry the same
genes, they could have
different alleles (different
versions of the same gene)
11. 3.2 U6 Diploid nuclei have pairs of homologous
chromosomes.
• Diploid nuclei have two copies of
each type of chromosome. One
chromosome comes from the
mother and one from the father.
• Haploid gametes (sperm and egg)
fuse during sexual reproduction
which produces zygote with a
diploid nucleus
• This cell will then divide by
mitosis to produce numerous
cells, all with a diploid nucleus
• Each nucleus has two copies of
each gene, accept the sex
chromosomes
12. 3.2 U.7 Haploid nuclei have one chromosome of each pair. [The two
DNA molecules formed by DNA replication prior to cell division are
considered to be sister chromatids until the splitting of the centromere
at the start of anaphase. After this, they are individual chromosomes.]
• Haploid nuclei have one copy of each chromosome or one full set of
the chromosomes in that particular species eg. Human 23
chromosomes
• These are called gametes, which are sperm and egg
• Human sperm and eggs each contain 23 chromosomes
https://classconnection.s3.amazonaws.com/116215/flashcards/771420/png/meiosis-1.png
13. 3.2 U.7 Haploid nuclei have one chromosome of each pair. [The two
DNA molecules formed by DNA replication prior to cell division are
considered to be sister chromatids until the splitting of the centromere
at the start of anaphase. After this, they are individual chromosomes.]
• Chromosome to the right
splits at the centromere.
• This occurs during
Anaphase
• The chromatids move to
opposite poles of the cell
to become chromosomes
in a newly created cell.
Chromosome
With two
Chromatids
Become Two
Chromosome
14. 3.2 U.8 The number of chromosomes is a characteristic
feature of members of a species.
• The chromosome number is a characteristic
feature of that species.
• A chromosome number does not indicate how
complicated an organism might be
• Organisms with different numbers of
chromosomes would unlikely be able to
interbreed
• Chromosome number tends to remain
unchanged over millions of years of evolution;
however, sometimes through evolution
chromosomes can fuse together or split to
change the number of chromosomes an
organism contains
• During human evolution, two ancestral ape
chromosomes fused to produce human
chromosome 2
15. 3.2 U.9 A karyogram shows the chromosomes of an organism in
homologous pairs of decreasing length. [The terms karyotype and
karyogram have different meanings. Karyotype is a property of a cell—
the number and type of chromosomes present in the nucleus, not a
photograph or diagram of them.]
http://upload.wikimedia.org/wikipedia/commons/f/f3/Mapa_gen%C3%A9tico_o_cariograma.jpeg
16. Karyotyping
•A karyotype is a picture of an organism's genetic make-up in which the
chromosomes of a cell have been stained so that the banding pattern
of the chromosomes appear.
•Cells in Metaphase are stained to show distinct parts of the
chromosomes. The cells are then photographed through a
microscope and enlarged.
•The chromosomes are cut from the photograph and arranged
according to size, shape, centromere position, and banding patterns.
http://www.mrothery.co.uk/module2/images/Image214.gif
17. 3.2 U.10 Sex is determined by sex chromosomes and
autosomes are chromosomes that do not determine sex.
• The X and Y chromosome determine the sex
of an individual
• The X chromosome contains over 2000 genes
in comparison to the Y chromosome has less
then 100 genes
• If an individual has two X chromosomes they
will be a female and if they have an X and a Y
chromosome they will be a male
• All other chromosomes are called autosomes
and do not affect the sex of an individual
• The X chromosome has many genes located
on it essential to human development, while
the Y chromosome has a small number of
genes (some of these are shared with the X
chromosome). The rest of the genes on the Y
chromosome are only necessary for male
development
http://images.zeit.de/wissen/gesundheit/2014
-01/y-chromosom/y-chromosom-540x304.jpg
18. 3.2 A.1 Cairns’ technique for measuring the length of
DNA molecules by autoradiography.
• Using the technique of autoradiography
Cairns first supplied the cells with suitable
radioactive material (replaces normal
hydrogen in thymidine).
• Used to selectively label only DNA and will
not label RNA.
• Intact bacterial chromosomes are placed on
slides. These slides are then covered by
photographic emulsion and stored in dark.
• During this storage the particles are emitted
exposing the film
• The photographs show the regions of
labelled DNA.
• The results demonstrated semi-
conservative mode of replication.
19. 3.2 A.2 Comparison of genome size in T2 phage, Escherichia coli, Drosophila
melanogaster, Homo sapiens and Paris japonica. [Genome size is the total length of DNA in an
organism. The examples of genome and chromosome number have been selected to allow
points of interest to be raised
Name Genome Length
(million base pairs)
Number of Genes
T2 phage (Virus) 0.18 300
Escherichia coli
(Bacteria)
5 4,377
Drosophila
melanogaster
(Fruit Fly)
140 17,000
Paris japonica
(Woodland Plant)
150,000 Unknown
Homo sapiens
(Human)
3,000 19-23,000
20. 3.2 A.2 Comparison of genome size in T2 phage, Escherichia coli, Drosophila
melanogaster, Homo sapiens and Paris japonica. [Genome size is the total length of DNA in an
organism. The examples of genome and chromosome number have been selected to allow
points of interest to be raised
Paris japonica
Largest Known Genome
21. 3.2 A.3 Comparison of diploid chromosome numbers of Homo
sapiens, Pan troglodytes, Canis familiaris, Oryza sativa, Parascaris
equorum.
Homo sapiens (46)
22. 3.2 A.3 Comparison of diploid chromosome numbers of Homo sapiens, Pan
troglodytes, Canis familiaris, Oryza sativa, Parascaris equorum.
Pan troglodytes (48)
http://static1.squarespace.com/static/51b89f0ce4b0000660671282/t/540785e0e4b00aec95acf4cb/1409779168825/floandfigan.jpg
23. 3.2 A.3 Comparison of diploid chromosome numbers of Homo
sapiens, Pan troglodytes, Canis familiaris, Oryza sativa, Parascaris
equorum.
Canis familiaris 78
https://c1.staticflickr.com/5/4007/5076413065_6a42962771_b.jpg
24. 3.2 A.3 Comparison of diploid chromosome numbers of Homo
sapiens, Pan troglodytes, Canis familiaris, Oryza sativa, Parascaris
equorum.
Species Name Number of
Chromosomes
Homo sapiens 46
Pan troglodytes 48
Canis familiaris 78
Oryza sativa 24
Parascaris
equorum
2
Rice: Oryza sativa
http://upload.wikimedia.org/wikipedia
/commons/6/65/Oryza_sativa_Kyoto_J
PN_001.JPG
Round Worm:
Parascaris equorum
http://www.vetnext.com/fotos/quizc2a4.jpg
25. Normal Male
3.2 A.4 Use of karyograms to deduce sex and diagnose Down syndrome
in humans.
http://commons.wikimedia.org/wiki/File:NHGRI_human_male_karyotype.png
26. Normal Female
3.2 A.4 Use of karyograms to deduce sex and diagnose Down syndrome
in humans.
27. Male with Down Syndrome: Trisomy 21; mental deficiencies ,
as well as physical abnormalities
3.2 A.4 Use of karyograms to deduce sex and diagnose Down syndrome
in humans.
http://upload.wikimedia.org/wikipedia/commons/6/6f/Trisomie_21_Genom-Schema.gif