Notas
Lec 2 - DNA & chromosomes
Conteúdo das notas (7)
Página 1
Meiosis
i) Stages of meiosis
Interphase I
Replication of chromosomal DNA
Prophase I
Chromatin condense to chromosomes
Homologus chromosomes pair up side by side in perfect alignment
In males - X & Y chromosomes line up end to end!
Homologus chromosomes intertwine @ attachment points
2 homologous chromosomes bivalent (2 chromatids form 1 unit)
Tetrad (4 sister chromatids)
Chiasma formation occurs
Attachment points @ which genetic crossing over occurs
Produces new possible gene combinations & new possible trait combinations
Bivalents move towards equitorial plate, spindle apparatus forms & nuclear membrane breaks down


Metaphase I
Same as mitosis
Anaphase I
Chiasmata disappear
Homologus chromosomes pulled to opposite sides cell by spindle fibres
Unlike in mitosis, centromeres do not split (sister chromatids aren't seperated)
Only 1/2 original number of chromosomes migrates towards each pole
i.e. In mitosis, if there are 4 chromosomes along equiplate - 4 chromatids migrate to each side of cell (splitting)
Whereas in meiosis, if there are 4 chromosomes along equiplate - 2 chromosomes migrate to each side
Telophase I
Chromosomes reach opposite sides of cell
Same as mitosis
2 daughter cells formed in males
1 daughter cell in females + primary polar body
Haploid
Each chromosome = 2 sister chromatids
Meiosis II occurs after this stage - leads to:
Formation of 4 functional haploid daughter cells in males
Formation of secondary oocyte & 2nd polar body in females
Remember only occurs after fertilisation in females!

ii) Cross over
See prophase I above
In males:
X & Y chromosome are not the same size & therefore cannot align perfectly
Pair tip-to-tip
Cross over occurs @ tip of short arm of X & Y chromosomes (pseudo-autosomal region)
These regions contain v similar DNA sequences
iii) Mitochondrial DNA inheritance
ONLY EVER INHERITED FROM MOTHER!!!
Due to fact that sperm only contribute a nucleus
Shed body containing mitochondria in order to enter egg
Ovum contains many copies of subcellular organelles of somatic body cells
All genes carried in mitochondrial genome passed on equally to offspring of both sexes
Mitochondria do not have DNA repair enzymes
High rate of spontaneous mutation
Página 2
Blood group antigens
i) Genotypes
Homozygous
AA - Group A
BB - Group B
OO - Group O
Heterozygous
AO - Group A
BO - Group B
AB - Group AB
ii) H antigen
Gene locus located on chromosome 19
Found on all 4 blood group types (A, B, AB, O)
Synthesises sequence of monomers which allow other RBC antigens to attach to RBC surface
iii) ABO group antigens
Gene locus located on chromosome 9
Group A = N-acetylgalactosamine glycosidically bonded to H/O antigen (see above)
Group B = D-galactose bonded to H/O antigen
Group O = Nothing bound to H/O antigen - caused by SND
iv) Homozygous blood group alleles
Homozygous AA blood group may have 2 different alleles of A:
Potential single nucleotide replacement which is 'silent'
Página 3
Cytogenetics
i) What is cytogenetics?
Cytogenetics = study of number & structure of chromosomes + associated abnormalities
Used to identify abnormalities that affect v small regions of genome
Identification DNA polymorphisms in parents & offspring
ii) Stages of karyotyping
Living tissue sample (usually blood) cultured in vitro for required length of time
Can also take:
T lymphocytes
Skin fibroblasts
Bone marrow
Chorionic villus cells
Metaphase arrest induced using colcemid
Cells are harvested & nucleus is ruptured
Chromosomes stained with designated nuclear stain & photographed
Images of 22 pairs of chromosomes arranged according to length
Karyogram
Sex chromosomes always put in right hand corner


iii) Nomenclature
Autosomes arranged according to size (where 1 = biggest)
Except 21 & 22!
21 is smallest
Location of gene loci on short arm = p (petit)
Location of gene loci on long arm = q
Chromosome regions counted from centromere outwards!
p1 = near centromere - p2 - p3 = near tip
q1 = near centromere - p2 - p3 = near tip
Regions on chromosomes divided into bands
i.e. 14q32 = second band in the 3rd region of long arm of chromosome 14
Sub-bands designated by decimal points following band number
i.e. 14q32.3 = third sub-band of band 2
iv) Limitations of conventional cytogenetics
Limited resolution
Changes need to be around 5-10Mb DNA to be visible
Cannot detect very small chromosomal changes
v) Molecular cytogenetics
Fluorescence in-situ hybridisation (FISH)
MOA
Labeled single-stranded DNA segment (probe which has been labelled with a fluorescent dye) exposed to denatured metaphase, prophase or interphase chromosomes from a patient
Probe undegoes complementary base pairing only with complementary DNA sequence @ specific location on one of the denatured chromosomes
Chromosomes are viewed under a fluorescence microscope

What is FISH used for?
Used to determine if portion of chromosome has been deleted
In unaffected person
Probe will hybridise in 2 places (due to presence 2 homologus chromosomes in somatic cell nucleus)
In an affected person
Probe will hybridise in 1 place (deletion of one of chromosomes)
Can also detect if there is an extra copy of a chromosome
Página 4
Trisomy 21
i) Case study & genetics
D.K.
First child
Mother aged 38
Father aged 51
Observation of child detected:
Hypotonicity
Single transverse crease across palm
Large tongue
Short fingers
Flat distinct facial profile

D.K. has trisomy 21
What is trisomy 21?
Common autosomal aneuploidy - person has 3 pairs of chromosome 21 - instead of normal 2 pairs
Clinically important features of trisomy 21 include:
Intellectual disability (can vary in severity)
GIT obstruction
Congenital heart defects
Respiratory infections
Extra 21 chromosome is contributed by mother in ~90% of cases
Strong correlation between maternal age & Down syndrome risk

ii) Aneuploidy
Cells that contain missing or additional chromosomes
Number of chromosomes in cell is not multiple of 23
Consist of monosomies & trisomies:
Monosomy = presence of only one copy of chromosome
Very uncommon - most do not survive to full term
Trisomy = 3 copies of a chromosome
More common - see among live births
Illustrates that body can tolerate excess genetic material more easily than a deficit in genetic material
Página 5
Chimeras
i) Case study & genetics
Mr & Mrs X had a son in June 2014
Healthy male
Blood group = AB
Mr X's blood group = A (AA or AO)
Mrs X's blood group = A (AA or AO)
How is it Mr & Mrs X's baby has a different blood group to them?
Wrong child?
Mr X is not the father?
Wrong sperm? (IVF)
Mr X is a chimera
Essentially a combination of 2 people!
How does this happen?
Chimeras start out as fraternal twins
2 seperate eggs have been fertilised by 2 seperate sperm around same time
If these 2 eggs develop seperately - you get fraternal twins!

In chimeras, instead of the two eggs developing seperately - one person ends up with both sets of cells
The 2 siblings fuse together to become one person
This means Mr X has some 'blue' cells & some 'red' cells -

When Mr X produces sperm
Some sperm will get his 'true' DNA...
Whilst others will get his 'twin' DNA
The sperm that fertilised Mrs X's egg to produce their son contained the 'twin' DNA
This led to the baby having some cells which carry the allele for attachment of N-acetylgalactosamine
& other cells which carry the allele that add D galactose!
http://genetics.thetech.org/node/313

Página 6
Acute promyelocytic leukemia
i) Case study
21 year old female
Presenting with extensive bruising & heavy vaginal bleeding
WBC count = low
Platelet count = low
Excess of promyelocytes in bone marrow
Patient has Acute promyelocytic leukaemia
ii) Genetics of APML
Translocation of genetic material between chromosome 15 & chromosome 17
Gene originally located 2nd band of 2nd part of long arm chromosome 15
Gene is transposed to 1st band of second part of long arm chromosome 17
iii) Use of FISH to detect AMPL gene

iv) Treatment
ATRA - vitamin A derivative
Interacts with RAR to induce cell differentiation & apoptosis
Página 7
Points to remember
Cros over during meiosis = homologus chromosome pairs mixing genetic information
Expression of genes can be monoallelic or biallelic - blood group antigens are biallelicaly expressed
Down's syndrome is an anueploidy where someone is born with 3 copies of chromosome 21
Trisomy 21 is the most common form of aneuploidy in live-born infants
Informações
- Descrição
- Genes, Gametes & Embryos (Genetics) Notas sobre Lec 2 - DNA & chromosomes , criado por Niamh McLoughlin em 06-11-2017.
- Criado por
- Niamh McLoughlin · nov 2017
- Atualizado
- 3 dez 2017
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