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Heredity
the transmission of traits from one generation to another
Genetics is the scientific study of
heredity and variation
Genes
units of heredity and made of segments of DNA
Gametes
genes passed to next generation via reproductive cells
Humans have
46 chromosomes
Asexual
a single individual passes all genes onto offspring without the fusion of gametes
A Clone is
group of genetically identical individuals from the same parent
Sexual reproduction
two parents give rise to offspring that have unique combinations of genes
Human somatic cells have
23 pairs of chromosomes
Karyotype
ordered display of the pairs of chromosomes from a cell
The sex chromosomes
x and Y
The remaining 22 pairs of chromosomes are
called autosomes
Females
xx
Males are made up of
xy
Homologous chromosomes
includes one chromosome from each parent
46 chromosomes are in
two sets of 23 one from mother one from father
Fertilization
union of gametes
Fertilized egg is called
zygote
The only type of human cells produced by meiosis
gametes
_____ results in one set of chromosomes in each gamete
Meiosis
Exhibit an alternation of generations
Plants and some algae
Diploid organism
called sporophyte and makes haploid spores by meiosis
Spore grows by
mitosis
Chromosomes duplicate
before meiosis
The stages of meiosis
prophase I, metaphase I, anaphase I, telophase I and cytokinesis.
Division of meiosis
prophase II, metaphase II, anaphase II, telophase II and cytokinesis.
Mitosis
conserves the number of chromosome sets, producing cells that are genetically identical to the parent cell.
Meiosis
reduces the number of chromosomes sets from two diploid to one haploid, producing cells that differ genetically from each other and parent cell.
Mutations
changes in organism’s DNA
Three mechanisms to genetic variation
Independent assortment of chromosomes, crossing over, Random fertilization.
Two laws of inheritance
The law of segregation and the law of independent assortment.
Pleiotrophy
most genes have multiple phenotypic effects.
Epistasis
expression of a gene at one locus alters the phenotypic expression of a gene at a second locus
Traits that depend on multiple genes combined with environmental influences are called
multifactorial
Phenotype
physical appearance, internal anatomy, Physiology and behavior, overall genotype
Pedigree
family tree that describes interrelationships of parents and children across generations
Recessively inherited disorders
show up only in individuals homozygous for the allele
Cystic Fibrosis
most common lethal genetic disease in USA
Sickle cell disease affects
one out of 400 African Americans
In amniocentesis
liquid bathes the fetus is removed and tested
In chorionic villus sampling (CVS)
sample of placenta is removed and tested
Phenylketonuria (PKU)
recessively inherited disorder that occurs in one of every 10,000 -15,000 births in the USA
A gene on the Y chromosome called SRY is responsible for
development of the testes in an embryo
X chromosome contains
1,100 genes
For a recessive X-linked trait to be expressed
a female needs two copies of the allele (homozygous), and a male needs only one copy (hemizygous)
In mammalian females
one of two X chromosomes in each cell is randomly inactivated during embryonic development
Each chromosome other than the Y chromosome
Have hundreds or thousands of genes
Linked genes
genes located on the same chromosome tend to be inherited together
Parental types
offspring with a phenotype matching one of the parental phenotypes
Recombinant types
offspring with nonparental phenotypes
Linkage map
genetic map of chromosome based on recombination frequencies
Large scale chromosomal alterations in humans and other mammals often lead to
spontaneous miscarriages, or lead to disorders
Plants tolerate
genetic changes better than animals
Nondisjunction
pairs of homologous chromosomes do not separate normally during meiosis
Polyploidy
condition in which an organism has more than two complete sets of chromosomes
Polyploidy is more common in
plants