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48 Cards in this Set

  • Front
  • Back
Mendel developed true-breeding strains to be used as ____
The parental generation, designated P
Look at table 12.1
:)
The progeny from the cross of the P parents are called what?
The first filial generation, designated F1
When F1 individuals are crossed to each other or self-fertilized what is it called?
Their progeny are designated F2
A monohybrid cross involves _____
One character (seed shape) and different traits (round or wrinkled)
Give an example of dominant and recessive traits
When crossing P1 pure-breeding round plants with wrinkled plants, the F1 seeds were all round; the wrinkled trait failed to appear at all.
Because the spherical trait completely masks the wrinkled trait when true-breeding plants are crossed, the spherical trait is considered dominant and the wrinkled trait recessive
What is the ratio of the F2 generation?
3:1
Look at figure 12.3
:)
What conclusions did mendel reach after his experiment?
The units responsible for inheritance are discrete particles that exist within an organism in pairs and separate during gamete formation.
Each pea has two units of inheritance for each character.
During production of gametes, only one pair for a given character passes to the gamete.
When fertilization occurs, the zygote gets one unit from each parent, restoring the pair
Mendel’s units of inheritance are now called _____
Genes
Different forms of a gene are called ___
Alleles
______individuals have two copies of the same allele (i.e., they are homozygous)
True-breeding
Some smooth-seeded plants are Ss or _______, although they will not be true-breeding
Heterozygous
What is Mendel’s first law?
is called the law of segregation: Each gamete receives one member of a pair of alleles.
They can be determined by means of a Punnett square
What is a locus?
It is a gene that is at a portion of the chromosomal DNA and resides at a particular site (called a locus) and that gene codes for a particular function
Look at figure 12.5
:)
What does Mendel’s second law state?
The law of independent assortment, states that alleles of different genes (e.g., Ss and Yy ) assort into gametes independently of each other
What are dihybrid crosses?
Hybrid crosses involving additional characters. They produce four possible gametes with a 9:3:3:1 ratio
Look at figure 12.7 and 10.8
:)
What are pedigrees?
They show phenotype segregation in several generations of related individuals because humans cannot be studied using planned crosses
Look at figure 12.5
:)
What does Mendel’s second law state?
The law of independent assortment, states that alleles of different genes (e.g., Ss and Yy ) assort into gametes independently of each other
What are dihybrid crosses?
Hybrid crosses involving additional characters. They produce four possible gametes with a 9:3:3:1 ratio
Look at figure 12.7 and 10.8
:)
What are pedigrees?
They show phenotype segregation in several generations of related individuals because humans cannot be studied using planned crosses. Pedigree outcomes for small samples fail to follow the expected outcomes closely
Look at figure 12.10
:)
Differences in alleles of genes consist of slight differences in the DNA sequence at the same locus, resulting in what?
Different protein products
How many allelels can a population have?
A population can have more than two alleles for a given gene.
Even if more than two alleles exist in a population, any given individual can have no more than two of them: one from the mother and one from the father
Describe incomplete dominance
Heterozygotes may show an intermediate phenotype which might seem to support the blending theory.
The F2 progeny, however, demonstrate Mendelian genetics. For self-fertilizing F1 pink individuals the blending theory would predict all pink F2 progeny, whereas the F2 progeny actually have a phenotypic ratio of 1 red:2 pink:1 white
Look at figure 12.12
:)
In codominance ____
Two different alleles for a gene are both expressed in the heterozygotes
In the human ABO blood group system the alleles for blood type are A, B, and O. What are the possible outcomes?
AA, or AO, results in type A.
BB, or BO, results in type B.
OO results in type O (O is completely recessive).
AB results in type AB. The alleles are called codominant
Look at figure 12.13
:)
What two factors determine the phenotype of an organism?
Genotype and environment
What can affect the translation of genotype into phenotype?
Variables such as light, temperature, and nutrition
What are controlled by groups of several genes?
Complex inherited characteristics. For example, human height
Variation is ________________ rather than qualitative
Continuous, or quantitative
Variation is usually due to what two factors?
Multiple genes with multiple alleles, and environmental influences on the expression of these genes
What is crossing over?
It is when homologous chromosomes exchange corresponding segments during prophase I of meiosis
Look at figure 10.19
:)
In mammals, sex is determined by what?
Which sex chromosomes you possess. The sex chromosomes are labeled as X and Y.
Describe the sex chromosomes
The sex chromosomes are labeled as X and Y.
Females have two X chromosomes.
Males have X and Y.
Females can only produce one type of egg – one containing a X.
Thus, sex of offspring is determined by the sperm – if a sperm containing an X chromosomes fertilizes the egg = female; if sperm contains a Y = male
How many genes does the y and x chromosomes have compared to each other?
The Y chromosome carries very few genes (about 20 are known), whereas the X carries a great variety of characters
Females with XX may be ______for genes on the X chromosome.
Heterozygous
Males with XY have how many copies of a gene?
Only one copy of a gene
What is sex-linked inheritance?
The transmission to successive generations of traits that are due to alleles
Look at figure 12.23
:)
Pedigree analysis of X-linked recessive phenotypes shows us what?
The phenotype appears much more often in males than in females.
A male with the mutation can pass it only to his daughters.
Daughters who receive one mutant X are heterozygous carriers.
The mutant phenotype can skip a generation if the mutation is passed from a male to his daughter and then to her son