3.2 Chromosomes
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The single prokaryotic chromosome is coiled up and concentrated in the nucleoid region.
Prokaryotes have two types of DNA: a single chromosome and plasmids.
Page 6: Features of Plasmids
Features of plasmids:
naked DNA (no histone)
small circular rings of DNA
not responsible for normal life processes
contain survival characteristics
can be passed between prokaryotes
can be incorporated into nucleoid chromosome
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Cairns' technique for measuring the length of DNA molecules by autoradiography.
John Cairns used autoradiography to visualize and measure DNA molecules in E. coli.
E. coli possesses a single circular chromosome that is 1,100 μm long.
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Cairns' technique for measuring the length of DNA molecules by autoradiography.
John Cairns produced images of DNA molecules from E. coli using autoradiography.
The images showed that E. coli possesses a single circular chromosome that is 1,100 μm long.
Cairns' images also provided evidence to support the theory of semi-conservative replication.
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Eukaryote chromosomes are linear DNA molecules associated with histone proteins.
Eukaryotic chromosomes may be up to 85mm in length.
DNA has to be coiled in a predictable fashion to fit into the nucleus.
Nucleosomes are formed by wrapping DNA around histone proteins.
Prokaryotic DNA is supercoiled but not organized by histones.
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Eukaryotes possess multiple chromosomes.
All individuals of a species possess the same chromosomes with the same gene loci.
Chromosomes can vary in length, position of the centromere, and genes at specific loci.
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Use of databases to identify the locus of a human gene and its polypeptide product.
Use the online database to search for genes and loci responsible for synthesizing specific polypeptides.
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The number of chromosomes is a characteristic feature of a species.
Chromosome number reflects the complexity of an organism.
Organisms with different numbers of chromosomes are unlikely to interbreed successfully.
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Diploid nuclei have pairs of homologous chromosomes.
Haploid nuclei have one chromosome of each pair.
Diploid nuclei have two copies of every gene, except for genes on the sex chromosomes.
Gametes have haploid nuclei, while the fertilized egg cell is diploid.
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Comparison of diploid chromosome numbers of different species.
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Comparison of diploid chromosome numbers of different species.
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Comparison of diploid chromosome numbers of different species.
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Homologous chromosomes carry the same sequence of genes but not necessarily the same alleles.
Somatic cell nuclei are diploid and contain homologous pairs of each chromosome.
Homologous chromosomes are the same size and carry the same genes at the same loci.
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Mammals, including humans, are diploid organisms.
Many other eukaryotes may have more than two copies of a particular chromosome.
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Humans have 23 pairs of chromosomes in diploid somatic cells.
One pair is the sex chromosomes (XX for female, XY for male).
The X chromosome is larger and carries more genes than the Y chromosome.
The presence of the SRY/TDF gene on the Y chromosome leads to male development.
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Chromosome pairs segregate in meiosis.
Females produce eggs containing the X chromosome.
Males produce sperm containing either X or Y chromosomes.
The SRY gene determines maleness.
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Genome size is the total number of DNA base pairs in one copy of a haploid genome.
Comparison of genome size in T2 phage, Escherichia coli, Drosophila melanogaster, Homo sapiens, and Paris japonica.
Homo sapiens has 3.2 billion base pairs.
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Comparison of genome size in T2 phage, Escherichia coli, Drosophila melanogaster, Homo sapiens, and Paris japonica.
Canopy plant (Paris japonica) has 150 billion base pairs.
Escherichia coli has 130 million base pairs.
T2 phage has 4.6 million base pairs.
Fruit fly (Drosophila melanogaster) has 164 thousand base pairs.
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A karyogram shows the chromosomes of an organism in homologous pairs of decreasing length.
Stains used to make the chromosomes visible also give each chromosome a distinctive banding pattern.
Karyogram is a diagram or photograph of the chromosomes present in a nucleus arranged in homologous pairs of decreasing length.
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Description of methods used to obtain cells for karyotype analysis (e.g., chorionic villus sampling and amniocentesis) and the associated risks.
Age of parents influences chances of non-disjunction.
It is advisable for mothers in a high-risk category to choose to have a prenatal test.
The risk of a child having a trisomy such as Down Syndrome increases greatly in older mothers.
Amniocentesis or chorionic villus samples can be taken and from them a karyotype can be constructed.
Data from a positive test can be used to decide the best course of action, which at times can be to abort the fetus.
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Chorionic villus sampling and amniocentesis can be carried out in the 16th week of pregnancy with around a 1% chance of a miscarriage.
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Chorionic villus sampling and amniocentesis can be carried out in the 11th week of pregnancy with around a 2% chance of a miscarriage.
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Process of karyotyping:
Add tissue and chemical to sample.
Stimulate mitosis.
Add chemical to transfer cells to a tube.
Incubate.
Stop mitosis and centrifuge.
Concentrate in layers.
Culture in a growth medium.
Put cells onto a microscope slide.
Transfer to a tube containing fixative.
Cut out chromosomes.
Identify and add stain to pictures.
Arrange and photograph chromosomes.
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Use of karyograms to deduce sex and diagnose Down syndrome in humans.
Karyograms can be used to determine sex and whether a person has Down Syndrome.
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Bibliography / Ack