chapter 11 introduction to genetics. chromosomes and cells two general types of cells –somatic...
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Chromosomes and Cells
Two general types of cells– Somatic cells-body cells that make up the
tissues and organs– Gametes-sex cells (eggs and sperm)
Chromosomes and Cells
Characteristic number of chromosomes in cells of each species’ body cells
Gametes have ½ of that number of chromosomes
Human body cells have 46 chromosomes in every body cell but only 23 chromosomes in each gamete
Chromosomes and Cells
Chromosomes are grouped in pairs (homologous pairs) according to size, shape, and genes they carry
There are 23 pairs of chromosomes in human cells– Pairs 1-22 are autosomes – Pair 23 is sex chromosomes
Chromosomes and Cells
Somatic cells are diploid (having the “normal” number of chromosomes / cell = 46 for human somatic cells)
Gametes are haploid (having ½ the normal number of chromosomes / cell = 23 for human gametes)– Gametes are haploid because the diploid
number is reinstated at fertilization
Meiosis
Germ cells undergo meiosis to produce gametes
Meiosis is a form of nuclear division that divides diploid cells into haploid cells– Reduces the number of chromosomes– Essential for sexual reproduction
Meiosis
Germ cells undergo meiosis to produce gametes
Meiosis is a form of nuclear division that divides diploid cells into haploid cells– Reduces the number of chromosomes– Essential for sexual reproduction
Comparing mitosis and meiosis
MITOSIS– 1 nuclear division– Begin with 1 diploid cell– End w/ 2 diploid cells– Occurs in somatic cells– Daughter cells are identical
MEIOSIS– 2 nuclear divisions– Begin w/1 diploid cell– End w/4 haploid cells– Occurs in gametes or sex cells– Daughter cells are NOT identical
11-4 Meiosis
Involves 2 nuclear divisions
Results in the production of gametes or sex cells (egg and sperm)
Reduction division to reduce the number of chromosomes by half in the gametes (chromosomes return to normal number at fertilization)
Meiosis I
Begin with a diploid cell
Prophase I– Homologous chromosomes pair up to form
TETRADS (4 chromatids per tetrad)– Crossing over occurs: chromatids exchange
genes to create larger genetic variation– Nucleolus and nucleus dissolve– Spindles begin to form
Meiosis I
Anaphase I– Homologous chromosomes separate and
begin moving to opposite poles
Telophase I and cytokinesis– Nuclear membranes form around each set of
chromosomes– Cell separates into two new cells – Each new cell is now HAPLOID
Meiosis II
Begin with 2 haploid cells
Prophase II– Nuclei dissolve– Chromosomes are visible
Metaphase II– Chromosomes line up at the equator of each
cell– Centromeres are attached to spindles
Meiosis II
Anaphase II– Chromatids split in each cell and move to
opposite poles
Telophase II and cytokinesis– Nuclei form around each set of chromosomes– Each cell divides into two new haploid cells
Results of Meiosis
4 haploid daughter cells that are NOT identical
These cells will develop into gametes in a process known as gametogenesis– Males: all 4 cells develop into sperm– Females: only 1 cell receives enough
cytoplasm to become an egg; the other 3 become polar bodies and are reabsorbed
11-1 Gregor Mendel
Father of genetics
Born 1822
Austrian Monk
Attended the University of Vienna
Did all genetic research in the gardens at the monastary
Studied pea plants
Pea plants
Naturally true-breeding (can self-fertilize)
Can manipulate pollination for cross breeding to produce hybrid offspring
Hybrids are offspring from two parents having contrasting characters for a trait
Traits studied on peas
Seed shape
Seed color
Seed coat color
Pod shape
Pod color
Flower position
Plant height
Genes
Genes are chemical factors that control traits
Located on chromosomes
Have alternate forms call ALLELES
Each individual has 2 alleles for each trait (one allele coming from the mother one coming from the father)
Dominant and recessive
Dominant traits– show in all generations– Represented by capital letters
Recessive traits– Absent in first generation but reappear in
second generation– Represented by lower-case letters
11-2 Probability
Probability is the likelihood that an event will occur.
Probabilities are used to predict the outcomes of genetic crosses
To show probabilities of genetic crosses Punnett Squares are used
Punnett Squares
Show all possible gene combinations
Can be used to predict and compare genetic variations that result from a cross
Show genotypes (genetic makeup) using letters
Relate phenotypes (physical characteristics)
Genotypes
Homozygous have two of the same alleles– rr– RR
Heterozygous have two different alleles– Rr– Tt
11-3 Independent assortment
Genes that segregate independently do NOT influence each other’s inheritance
Genes are not inherited together
Leads to large variations in genetics of offspring
Crosses
Monohybrid cross involves one trait
Dihybrid cross involves two traits
P1 generation- true-breeding parents
F1 generation-first generation of hybrid offspring from P1
F2 generation-second generation of hybrid offspring (F1 parents)
Mendel’s principles
Inheritance of characteristics is determined by genes
Genes may have alternate forms called alleles; some dominant, some recessive
In sexually reproducing organisms, adults have 2 copies (alleles) for each gene-one from each parent
Alleles segregate independently
Incomplete dominance
Neither allele is completely dominant over the other
Heterozygotes will exhibit a “mixing” of traits or an intermediate phenotype
Multiple alleles
More than 2 alleles involved with the trait of that particular population
Rabbit fur color– C – brown; cch-gray, ch-white w/ brown areas,
c-albino
Polygenic traits
Traits produced by the interaction of several genes
At least 3 genes involved
Example: human skin color or human height
Genetic recombination
Sexual reproduction gives genetic variation in the offspring– Due to independent assortment of
chromosomes in meiosis– Mixing of alleles when gametes fuse in
fertilization– Produces unique combinations of alleles
Genetic recombination
Crossing over– Increases genetic variation– Occurs only in prophase I of meiosis– Chromatids of homologous chromosomes will
exchange (trade) some alleles
Genetic linkage
Genes located close together on a chromosome are usually inherited together because they are “linked”
Genes located far apart or on different chormososmes are inherited independently