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Science Test 28/05
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DNA
The
blueprint
of life
Features
such as hair colour, freckles and susceptibility to certain diseases tend to run in families. We inherit these features from our
parents.
The DNA in our cells carries the information that makes us who we are. This DNA originally came from an
egg
and a
sperm
produced by your parents.
Characteristics that are passed from
parent
to child are said to be
inherited.
Characteristics are passed from
both
parents.
It is impossible for
two
brown-eyed parents to have a child with
blue
eyes.
Your weight is determined by your
genetic
make-up to some extent.
A woman who eats a high protein diet during the first
2
months of pregnancy is more likely to give birth to a
son.
It is possible for a person to carry a
gene
for a
genetic disorder
and not know it.
Some
types of cancers are
hereditary.
Identical twins are
natural
clones.
In the majority of cases, genetic disorders are due to a problem with the
mother's egg
cells rather than the
father's sperm
cells.
A brother and sister who are
twins
have exactly the
same
DNA.
Gene
A piece of DNA (
deoxyribonucleic acid
)
DNA
A chemical found in the nucleus of cells that contains the
instructions
for constructing a particular
polypeptide
Protein
Containing one or more
polypeptides
, can determine
characteristics
Chromosome
Made up of DNA and other substances, including proteins, that can be seen using a
light
microscope when a cell is about to
divide
Most of the cells of healthy humans contain
23
matching pairs of chromosomes.
Karyotype
A picture showing the chromosomes
organised
in matching pairs in order of
size
from biggest to smallest
People who have Down syndrome have
47
rather than
46
chromosomes in their cells.
In Turner syndrome the karyotype reveals that there are only 45 chromosomes. Instead of two
sex
chromosomes there is only one
X
chromosome.
The platypus has
10
sex chromosomes.
Mitosis
1. Produces
daughter
cells with the same number and type of
chromosomes
as the parent cell
2. Occurs in certain parts of plants including the tips of the
roots
and
stems
3. Turns a single
fertilised
egg into the
trillions
of cells that make up an adult human
4. Produces new
skin
cells to replace those
lost
Gametes contain only
half
the number of chromosomes of other body cells.
Cytokinesis
is the process where the cell membrane pinches in so that the cell divides in two after mitosis has occurred.
Dr Elizabeth Blackburn discovered an important enzyme called
telomerase
that maintains and repairs the
telomeres
at the end of chromosomes.
Mitosis
is a type of cell division that produces daughter cells with the same number of
chromosomes
as the parent cell
Meiosis
is a type of cell division that produces
daughter
cells with half the number of chromosomes as the parent cell
Meiosis produces
gametes
In
gametes
the chromosomes are not in
pairs
Meiosis
1. Chromosomes line up in matching pairs (homologous pairs)
2. Homologous pairs separate
3. Chance determines which cell gets the maternal or
paternal
chromosome from each pair
Humans
have 23 pairs of chromosomes, so there are 2^23 or 8,388,608 different ways the chromosomes can be divided during
meiosis
Chromosomes can swap sections when in
homologous pairs
, further
increasing
variation
At fertilisation, a male and female gamete combine to form a
zygote
with a
diploid
number of chromosomes
The zygote's chromosomes are copied during
mitosis
, so all body cells have the same
chromosomes
as the zygote
Sex
chromosomes
Females have two X chromosomes, males have
one
X and
one
Y chromosome
The sex of a baby is determined by whether the
sperm cell
that fertilises the egg contains an X or
Y chromosome
A sperm cell with an X chromosome results in a baby girl, a sperm cell with a
Y
chromosome results in a baby
boy
A mother's diet during pregnancy has
no effect
on the sex of the baby
Sex
selection technology can be used to increase the chances of having a child of a particular
sex
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