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AP Bio Notes on Meiosis- Ch. 13
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_Asexual_ reproduction produces offspring by mitosis that are _identical_
to each other and original parent. These identical offspring are called _clones_.
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_Sexual_ reproduction provides for
genetic _variation_ - the offspring have combined traits of the parents that make them _different_ from their parents and their siblings. This is very important because these new trait combinations may make them _better_ or worse off in their environment than others in their family or species.
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Chromosome Numbers _Somatic Cell – any _body_ cell except egg or sperm cells (Ex. skin cell, blood cell, bone cell, etc) Each somatic cell has its chromosomes in pairs called _homologous_ chromosomes or _homologues_. Each chromosome has thousands of _genes_ (gene = part of a DNA strand that causes a certain _trait_ such as eye color, hair type, lactose intolerant, etc)
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Homologous chromosomes are the same _size_, shape and have information for the
same _traits_. The place on a chromosome where a particular gene is found is called its _locus_ (loci is plural).
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Diagram:
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Special chromosomes called _sex _chromosomes_ determine your sex.
_X chromosome_ – a large sex chromosome _Y chromosome_ – a small sex chromosome In humans, a _female__ has two X chromosomes. XX = female A _male_ has one X and one Y chromosome. XY = male
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Different _organisms_ have different numbers of _chromosomes_.
_Autosomes_ – all other chromosomes except sex chromosomes Different _organisms_ have different numbers of _chromosomes_. Ex. Humans have 46 (23 pairs), a fly has 12 (6 pairs), a dog has 78 (39 pairs) A _diploid_ cell has its chromosomes in _pairs_. All __somatic__ cells are diploid cells.
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_Gametes_ are reproductive cells such as
_egg_ or _sperm_ cells. Gametes have only _1_ chromosome from each homologous pair of chromosomes. This is so that when they join, the new cell will have the right number of chromosomes.
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Diagram:
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Fertilization_ – when an egg and sperm join to make a new cell
_Zygote_ – new cell made when egg and sperm join (fertilized egg) A _Haploid_ cell has only _1_ copy of each kind of chromosome. Eggs and sperm are _haploid_. The zygote is _diploid_.
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If the haploid number of chromosomes is n, the diploid number is 2n.
Ex. In humans, n = 23 so the diploid number is 2n = 2x23 = 46
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Eggs and sperm can not be produced by mitosis or they would not be _haploid_.
Instead, they are made by _meiosis_. In meiosis new cells are made – each with only _1_ copy of each chromosome type. No homologous pairs.
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Overview of Meiosis
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Stages of Meiosis The time between meiotic divisions is still called _interphase_ and the DNA is still copied by replication during the _synthesis_ stage as usual.
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The cell that begins the process of meiosis is always a _diploid_ _somatic_ cell.
Remember, meiosis _makes_ gametes. It does _not_ occur _in_ gametes!
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1. Prophase I A. Chromatin coils into doubled __chromosomes__
B. Nuclear envelope and nucleolus __disintegrate__ C. _spindle_ forms
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Prophase I continued **D. _Synapsis_ occurs -
Homologous chromosomes _line_ _up_ next to each other to form a group of 4 chromatids called a _tetrad_.
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Tetrad
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Prophase I continued **_Crossing_ _over_ can occur–
part of one _chromatid_ breaks off and is exchanged with the same part of a chromatid of its _homologous_chromosome)
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Crossing over
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Prophase is the longest stage of meiosis.
Prophase I continued The place where the 2 chromatids overlap is called _chiasma__ (chiasmata = plural) Prophase is the longest stage of meiosis.
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2. Metaphase I Pairs of the _homologous_ chromosomes line up on the equator
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Metaphase I
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3. Anaphase I Homologous chromosomes _move_ to opposite ends of the cell.
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Anaphase I
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Telophase I __Cytokinesis_ occurs.
(Some cells uncoil the chromosomes and form new nuclear membranes and nucleoli, but most cells skip this since the division process is going to continue.)
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Telophase I
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5. Prophase II New _spindle_ forms
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Metaphase II Chromosomes line up on _metaphase_ _plate_in single file.
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Metaphase II
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Anaphase II Centromeres divide and _chromatids_(single chromosomes) go to opposite poles.
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Anaphase II
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Telephase II New nuclear _membranes_ and __nucleoli_ form.
__Spindle_ breaks up Chromosomes uncoil into __chromatin__ _Cytokinesis_ occurs
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Telophase II
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Now have _4_ _haploid_ cells!
__Spermatogenesis__ – meiosis in males to produce sperm. Makes four sperm as each haploid cell grows a tail.
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Watch meiosis video clip
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Diagram of spermatogenesis
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_Oogenesis_ – meiosis to produce an egg cell in females.
Cytokinesis is __unequal_ each time and only one large cell becomes an egg cell or _ovum_. The other three small cells are called _polar_ _bodies_. They die in animal cells.
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Oogenesis
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3 sources of genetic variability
(Make offspring different from each other) 1. Independent assortment 2. Random fertilization 3. Crossing over
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_Independent_ _assortment_ – homologous chromosomes are distributed randomly during meiosis – you can get either chromosome of each pair. This creates many possible combinations of chromosomes in the gametes.
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Ex. Humans have 23 pairs, so 223 (about _8_ _million_) combinations are possible in an egg or sperm!
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2. Random Fertilization Because two gametes join, there are 223 x 223 = 64 _trillion_ possible chromosome combinations in the children of two certain parents.
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3. Crossing over Crossing over creates even more possibilities so the different possible gametes is almost _unlimited_.
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Chromosome problems A person with the wrong number of chromosomes may or may not be _normal_. Ex. _Trisomy_ _21_ or Down’s syndrome – this person has three copies of chromosome number 21. Will have varying degrees of mental retardation
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Down’s syndrome
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Down’s syndrome
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Can be caused by _nondisjunction__ – when chromosomes do not separate properly during cell division.
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Diagram of nondisjunction during meiosis I
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Diagram of nondisjunction during meiosis II
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__Karyotype_ – a photo of chromosomes during division in which chromosomes are arranged in pairs to see if they are correct.
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Karyotype
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Karyotype
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Risk of nondisjunction and Down’s syndrome _increases_ as a woman ages.
_Amniocentesis_ – amniotic fluid is taken from around a baby in the uterus to make a karyotype to check for chromosome problems in the baby.
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Other disorders caused by nondisjunction:
Turner syndrome: A female with only 1 X chromosome. This girl will be sterile (unable to have children) because her sex organs will not mature.
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Turner syndrome continued
Estrogen replacement therapy can help with development of secondary sex characteristics. Most have normal intelligence. Occurs in 1 out of 5,000 births.
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B. Kleinfelter syndrome:
A male with XXY sex chromosomes. The testes are abnormally small and he will be sterile. He will also have subnormal intelligence. Occurs in 1 out of 2,000 births.
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