Unit 5: Heredity
Heredity: the transmission of traits from one generation to the next
Variation: demonstrated by the differences in appearance that offspring show from parents and siblings
Genetics: the scientific study of heredity and variation
Genes: the units of heredity and are made up of segments of DNA
Gametes (sperm and eggs): are the reproductive cells that pass genes on to the next generation
Each gene has a specific position, or locus, on a certain chromosome
A clone is a group of genetically identical individuals from the same parent (from asexual reproduction)
Karyotype: an ordered display of the pairs of chromosomes from a cell
The two chromosomes in each pair are called homologous chromosomes, or homologs
Meiosis: cell division that creates gametes
Meiosis takes place in two sets of cell divisions, called meiosis Iand meiosis II resulting in four (haploid - 23 chromosomes) daughter cells, rather than the two (diploid - 46 chromosomes) daughter cells in mitosis
A gamete (sperm or egg) contains a single set of chromosomes and is haploid (n) (product of meiosis)
Our cells contain 23 homologous pairs of chromosomes (one from each parent) totalling 46
During S-phase the chromosomes are replicated resulting in sister chromatids
Homologs may have different versions of genes, each called an allele
In crossing over, nonsister chromatids exchange DNA segments
Each homologous pair has one or more X-shaped regions called chiasmata β this is where crossing over occurs.
A zipper-like structure called the synaptonemal complex forms during this attachment (synapsis)
The DNA breaks are closed so that a paternal chromatid is joined to a piece of maternal chromatid, and vice versa
true-breeding - plants that produce offspring of the same variety when they self-pollinate
hybridization - crossing two different, true-breeding varieties (resulting in a hybrid)
Law of Segregation: when an organism makes gametes, each gamete receives just one gene copy, which is selected randomly
An organism with two identical alleles for a character is said to be homozygous for the gene controlling that character (ex. AA or aa)
An organism that has two different alleles for a gene is said to be heterozygous for the gene controlling that character (ex: Qq)
Heterozygotes are not true-breeding, unlike homozygotes
Phenotype - physical appearance
Genotype - genetic makeup (alleles ex: Bb)
Law of independent assortment: states that each pair of alleles segregates independently of any other pair during gamete formation
*Genes located near each other on the same chromosome tend to be inherited together (gene linkage)
Incomplete dominance: the phenotype of F1 hybrids is somewhere between the phenotypes of the two parental varieties
Codominance: two dominant alleles affect the phenotype in separate, distinguishable ways
Multiple Alleles (common in many populations): when genes have more than two allelic forms
For example, the four phenotypes of the ABO blood group in humans are determined by three alleles of the gene IA, IB, and i.
Sex-linked gene: A gene that is located on either sex chromosome
X-linked genes: What genes on the X chromosome are called
For a recessive X-linked trait to be expressed
A female needs two copies of the allele (homozygous
A male only needs one copy of the allele (hemizygous)
X-linked recessive disorders are much more common in males than in females.
Most genes have multiple phenotypic effects, a property called pleiotropy
Quantitative characters are those that vary in population along a continuum/spectrum
Quantitative variation usually indicates polygenic inheritance, an additive effect of two or more genes on a single phenotype.
eg. skin color
Epistasis: when a gene at one locus alters the phenotypic expression of a gene at a second locus
A pedigree is a family tree that describes the interrelationships of parents and children across generations
Heredity: the transmission of traits from one generation to the next
Variation: demonstrated by the differences in appearance that offspring show from parents and siblings
Genetics: the scientific study of heredity and variation
Genes: the units of heredity and are made up of segments of DNA
Gametes (sperm and eggs): are the reproductive cells that pass genes on to the next generation
Each gene has a specific position, or locus, on a certain chromosome
A clone is a group of genetically identical individuals from the same parent (from asexual reproduction)
Karyotype: an ordered display of the pairs of chromosomes from a cell
The two chromosomes in each pair are called homologous chromosomes, or homologs
Meiosis: cell division that creates gametes
Meiosis takes place in two sets of cell divisions, called meiosis Iand meiosis II resulting in four (haploid - 23 chromosomes) daughter cells, rather than the two (diploid - 46 chromosomes) daughter cells in mitosis
A gamete (sperm or egg) contains a single set of chromosomes and is haploid (n) (product of meiosis)
Our cells contain 23 homologous pairs of chromosomes (one from each parent) totalling 46
During S-phase the chromosomes are replicated resulting in sister chromatids
Homologs may have different versions of genes, each called an allele
In crossing over, nonsister chromatids exchange DNA segments
Each homologous pair has one or more X-shaped regions called chiasmata β this is where crossing over occurs.
A zipper-like structure called the synaptonemal complex forms during this attachment (synapsis)
The DNA breaks are closed so that a paternal chromatid is joined to a piece of maternal chromatid, and vice versa
true-breeding - plants that produce offspring of the same variety when they self-pollinate
hybridization - crossing two different, true-breeding varieties (resulting in a hybrid)
Law of Segregation: when an organism makes gametes, each gamete receives just one gene copy, which is selected randomly
An organism with two identical alleles for a character is said to be homozygous for the gene controlling that character (ex. AA or aa)
An organism that has two different alleles for a gene is said to be heterozygous for the gene controlling that character (ex: Qq)
Heterozygotes are not true-breeding, unlike homozygotes
Phenotype - physical appearance
Genotype - genetic makeup (alleles ex: Bb)
Law of independent assortment: states that each pair of alleles segregates independently of any other pair during gamete formation
*Genes located near each other on the same chromosome tend to be inherited together (gene linkage)
Incomplete dominance: the phenotype of F1 hybrids is somewhere between the phenotypes of the two parental varieties
Codominance: two dominant alleles affect the phenotype in separate, distinguishable ways
Multiple Alleles (common in many populations): when genes have more than two allelic forms
For example, the four phenotypes of the ABO blood group in humans are determined by three alleles of the gene IA, IB, and i.
Sex-linked gene: A gene that is located on either sex chromosome
X-linked genes: What genes on the X chromosome are called
For a recessive X-linked trait to be expressed
A female needs two copies of the allele (homozygous
A male only needs one copy of the allele (hemizygous)
X-linked recessive disorders are much more common in males than in females.
Most genes have multiple phenotypic effects, a property called pleiotropy
Quantitative characters are those that vary in population along a continuum/spectrum
Quantitative variation usually indicates polygenic inheritance, an additive effect of two or more genes on a single phenotype.
eg. skin color
Epistasis: when a gene at one locus alters the phenotypic expression of a gene at a second locus
A pedigree is a family tree that describes the interrelationships of parents and children across generations