Meiosis and Sexual Reproduction
Loosely coiled - euchromatic
active chromatin
can be transcribed by RNA polymerase and transcription factors to make proteins
Tightly coiled - heterochromatin
inactive chromatin
genes hardly ever transcribed
compact chromosomes more easily moved than extended chromatin
Most chromosomes have both compaction levels
Interphase
divided into 3 phases: G1 = 1st Gap
cell doing its “everyday job”
S = DNA Synthesis
copies chromosomes
G2 = 2nd Gap
prepares for division
cell grows (more)
produces organelles, proteins, membranes
Cell Cycle
cell have a “life cycle”
Cell is formed from miotic division
Cell grows and matures to divide again
G1, S, G2, M
Epithelial cells, blood cells, stem cells
Some cells grow, mature, and divide to never divide again
G1 -> G0
Brain/nerve cells, muscle cells
Liver cell can come out of G0 and go through phases, then rest again
Copying/Replicating DNA
S - Synthesis phase of Interphase
dividing cell replicates DNA
must separate DNA copies correctly to 2 daughter cells
human cell duplicates ~3 meters DNA
each daughter cell gets complete identical DNA
error rate = ~1 per 100 million bases
3 billion base pairs in mammalian genome
Mitosis- produce cells with same information, identical daughter cells
Chromosomes are replicated in S phase of interphase then halved prior to fertilization
Parents are diploid (2n)
Meiosis produces haploid (n) gametes
Haploid cells contain a single set of chromosomes
If there were no reduction of chromosomes in meiosis the number of chromosomes would double each generation
Gametes fuse in fertilization to form a diploid (2n) zygote
The zygote becomes the next diploid (2n) generation
If meiosis goes wrong, gametes contain the wrong number of chromosomes
Meisos = reduction division
special cell division in sexually reprudocing organisms
reduce 2n -> 1n
diploid -> haploid (half)
makes gametes (sperm, eggs)
Meiosis 1: diploid cell enters prophase 1, homologous chromosomes separate leaving Haploid cells with pairs of sister chromatids (n)
Meiosis 2: sister chromatids separate leaving 4 haploid cells with individual chromosomes with no homologous pairing (n)
Double division of meiosis:
1st division separates homologous pairs
2nd division separates sister chromatids
1st step of Meiosis
meiosis evolved after mitosis
convenient to use “machinery” of mitosis
DNA replicated in S phase of meiosis (just like mitosis)
Asexual reproduction (Mitosis, binary fission, etc): produces genetically identical clones, advantageous when the environment is stable
Sexual reproduction
Mutations can generate variation in offspring
Random fertilization: union of male and female gametes
Meiosis brings about genetic variation in two key ways: Crossing over and Independent assortment
Crossing Over
During prophase 1
homologous pairs swap pieces of chromosome
sister chromatids intertwine
“synapsis”
Exchange of genetic material between non sister chromatids
May occur several times in each chromosome
Holds homologous together aligns DNA of non-sister chromatids, allows crossing over to occur
Homologues separate and are distributed to different cells
Meiosis 1: 1st division of meiosis separates homologous pairs (2n -> 1n)
interphase 1
prophase 1
metaphase 1
anaphase 1
telophase 1
Meiosis 2: 2nd division of meiosis separates sister chromatids (1n -> 1n)
prophase 2
metaphase 2
anaphase 2
telophase 2
Meiosis and crossing over introduce great genetic variation to population and drives evolution
Random assortment in humans produces 2^23 (8,388,608) different combinations
Any 2 parents will produce a zygote with over 70 trillion (2^23 x 2^23) diploid combinations
Prophase I: Crossing over
Anaphase I: Homologs separate
Anaphase II: Sisters separate
Changes in Chromosome Number and Structure
Euploidy is the correct number of chomrosomes in a species for multiples of that set
Aneuploidy is a change in the chromosome number resulting from nondisjunction
Nondisjunction (Failure of separation):
homologos chromosomes do not separate normally during anaphase I
sister chomarids did not separate normally during anaphase II
result in gain or loss of chromosomes
- one gamete receives two of the same type of chromosome, and another gamete receives no copy
Aneuploidy results from fertilization involving gametes in which nondisjunction occurred.
Offspring with this condition have an abnormal number of a particular chromosome.
Monosomic zygote only has one copy of a particular chromosome (Almost all result in miscarriage, except X0)
Trisomic zygote has three copies of a particular chromosome (Down syndrome)
Tuner syndrome (X0) - monomsy
female with a single X chromosome
Shoer, broad chest and widely spaced nipples
Can be of normal intelligence and function with hormone therapy
Klinfelter syndrome (XXY) - trisomy
male with underdeveloped testes and prostate, some breast development
long arms and legs, large lands
near-normal intelligence unless XXXY, XXXXY, etc
no matter how many X chromosomes are present, the presence of a chromosome Y renders in the male
Environmental agents like radiation, organic chemicals, or certain viruses can cause chromosome breakage
If broken ends of chromosomes don’t rejoin, mutations can occur
Human Syndromes
changes in chromosomes can cause various syndromes
Williams syndrome: loss of end of chromosome 7
Alagille syndrome: translocation between chromosome 2 and 20
Chronic myelogenous leukemia: blood cancer caused by translocation between chromosomes 22 and 9
Plants and haploid multicellular “individuals” alternate with diploid multicellular “individuals”
Haploid individual is the gametophyte
Diploid individual os the sporophyte
Meiosis only occurs during gametogenesis
production of sperm = spermatogenesis: all 4 cells become sperm
production of eggs = oogenesis
one of the four nuclei recives the majority of the cytoplasm
becomes the egg or ovum
others wither away as polar bodies