Campbell Biology: Ninth Edition - Chapter 14&15 Mendel and the Gene Idea

Campbell Biology: Ninth Edition - Chapter 14&15 Mendel and the Gene Idea

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Section 1

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In carrying out his breeding studies, Mendel examined characters that had which of the following properties? (eText Concept 14.1) They were controlled by loci that were (or behaved as if they were) on different chromosomes. It was possible to isolate true-breeding varieties for each trait. The traits varied in an either-or fashion. The characters each were controlled by a single gene. All of the listed responses are correct.

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Cards (97)

Section 1

(50 cards)

In carrying out his breeding studies, Mendel examined characters that had which of the following properties? (eText Concept 14.1) They were controlled by loci that were (or behaved as if they were) on different chromosomes. It was possible to isolate true-breeding varieties for each trait. The traits varied in an either-or fashion. The characters each were controlled by a single gene. All of the listed responses are correct.

Front

All of the listed responses are correct.

Back

Trait

Front

One of two or more detectable variants in a genetic character.

Back

Pea plants are tall if they have the genotype TT or Tt, and they are short if they have genotype tt. A tall plant is mated with a short plant. Which outcome below would indicate that the tall parent plant was heterozygous? (eText Concept 14.1) All of the offspring are short. All of the offspring are tall. The ratio of tall offspring to short offspring is 3:1. The ratio of tall offspring to short offspring is 1:1. There is not enough information to answer the question.

Front

The ratio of tall offspring to short offspring is 1:1.

Back

Phenotype

Front

Expressed. The observable physical and physiological traits of an organism, which are determined by its genetic makeup.

Back

A = big apples; R = red apples; a = small apples; r = yellow apples. You have one tree that produces big yellow apples and another tree that produces small red apples. When the two are crossed, you find that half of the new trees produce big red apples and half produce big yellow apples. What are the genotypes of the parents? (eText Concept 14.1) AArr and aaRr Aarr and aaRr AARr and Aarr AaRr and AaRr AaRr and aarr

Front

AArr and aaRr

Back

Concept Check 14.1 What if? List all gametes that could be made by a pea plant heterozygous for seed color, seed shape, and pod shape (YyRrIi; see Table 14.1). How large a Punnett square would you need to draw to predict the offspring of a self-pollination of this trihybrid?

Front

See table

Back

Concept 14.3 Inheritance Patterns are often more complex than predicted by simple Mendelian Genetics

Front

...

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Recessive Allele

Front

An allele whose phenotypic effect is not observed in a heterozygote.

Back

If an organism that is homozygous dominant is crossed with a heterozygote for that trait, the offspring will be _____. (eText Concept 14.1) all of the dominant phenotype 1/4 of the recessive phenotype all homozygous dominant all homozygous recessive present in a 9:3:3:1 ratio

Front

All of the dominant phenotype

Back

The Law of Independent Assortment

Front

Mendel's second law, stating that each pair of alleles segregates, or assorts, independently of each other pair during gamete formation; applies when genes for two characters are located on different pairs of homologous chromosomes or when they are far enough apart on the same chromosome to behave as though they are on different chromosomes.

Back

Which choice below is a basic difference between Mendel's particulate hypothesis and the hypothesis of blending inheritance? (eText Concept 14.1) The blending inheritance hypothesis, but not the particulate hypothesis, maintained that mutation is the major source of new gene combinations. The blending inheritance hypothesis, but not the particulate hypothesis, maintained that the two alleles at any given locus are always different. The blending inheritance hypothesis, but not the particulate hypothesis, maintained that the traits governed by genes in the egg are different from the traits governed by genes in the sperm. The blending inheritance hypothesis, but not the particulate hypothesis, maintained that after a mating, the genetic material provided by each of the two parents is mixed in the offspring, losing its individual identity. All of the listed responses are correct.

Front

The blending inheritance hypothesis, but not the particulate hypothesis, maintained that after a mating, the genetic material provided by each of the two parents is mixed in the offspring, losing its individual identity. The blending hypothesis maintained that the genetic material contributed by the two parents mixes in a manner analogous to the way blue and yellow paints blend to make green.

Back

Complete dominance

Front

The situation in which the phenotypes of the heterozygote and dominant homozygote are indistinguishable.

Back

Monohybrid Cross

Front

A cross between two organisms that are heterozygous for the character being followed (or the self-pollination of a heterozygous plant).

Back

The Law of Segregation

Front

Mendel's first law, stating that the two alleles in a pair segregate (separate from each other) into different gametes during gamete formation.

Back

Heterozygous

Front

Having two different alleles for a given gene.

Back

P Generation

Front

The true-breeding (homozygous) parent individuals from which F1 hybrid offspring are derived in studies of inheritance; P stands for "parental."

Back

Concept Check 14.1 Make Connections. In some pea plant crosses, the plants are self-pollinated. Refer back to Concept 13.1 (pp. 248-249) and explain whether self-pollination is considered asexual or sexual reproduction.

Front

Asexual

Back

The F1 generation differed from the F2 in Mendel's experiments in that _____. (eText Concept 14.1) all of the F1 showed the dominant phenotype, whereas only half of the F2 did all of the F1 showed the dominant phenotype, but only three-fourths of the F2 did all of the F1 showed the dominant phenotype, and all of the F2 showed the recessive phenotype one-half of the F1 showed the dominant phenotype, and three-fourths of the F2 did none of the F1 showed the dominant phenotype, but one-half of the F2 did

Front

all of the F1 showed the dominant phenotype, but only three-fourths of the F2 did

Back

F2 generation

Front

The offspring resulting from interbreeding (or self-pollination) of the hybrid FF1 generation.

Back

The law of independent assortment _____. (eText Concept 14.1) states that the alleles at different loci segregate independently from one another during a dihybrid cross can account for a 9:3:3:1 ratio seen in the F2 generation applies only to genes that are present on different chromosomes (or behave as if they were) The first and second answers are correct. The first, second, and third answers are correct.

Front

The first, second, and third answers are correct.

Back

Genotype

Front

The genetic makeup, or set of alleles, of an organism.

Back

In a certain plant, the alleles A, B, and C are completely dominant to the alleles a, b, and c. A plant with the genotype AABbcc will have the same phenotype as a plant with the genotype _____. (eText Concept 14.1) Aabbcc aabbcc AaBBcc AABBCc None of the listed responses is correct.

Front

AaBBcc

Back

Homozygous

Front

Having two identical alleles for a given gene.

Back

The multiplication rule

Front

A rule of probability stating that the probability of two or more independent events occurring together can be determined by multiplying their individual probabilities.

Back

The addition rule

Front

A rule of probability stating that the probability of any one of two or more mutually exclusive events occurring can be determined by adding their individual probabilities.

Back

What is indicated when a single-character testcross yields offspring that all have the dominant phenotype? (eText Concept 14.1) The parent with the dominant phenotype was homozygous. The parent with the dominant phenotype was heterozygous. Epistasis has occurred. The alleles are codominant. Both parents are heterozygous.

Front

The parent with the dominant phenotype was homozygous.

Back

If a plant variety is true-breeding for a dominant trait, then _____. (eText Concept 14.1) if the plant were allowed to self-pollinate, the dominant and recessive traits would consistently appear in a 3:1 ratio among the progeny the plant is heterozygous for the trait if the plant were crossed with a heterozygote, one-half of the progeny would show the dominant trait, and one-half would show the recessive trait if the plant were allowed to self-pollinate, all of the progeny would have the dominant trait the variety is unable to mutate

Front

if the plant were allowed to self-pollinate, all of the progeny would have the dominant trait

Back

Allele

Front

Any of the alternative versions of a gene that may produce distinguishable phenotypic effects.

Back

Phenotype

Front

The EXPRESSED/observable physical and physiological traits of an organism, which are determined by its genetic makeup.

Back

What is Mendel's Second Law?

Front

The Law of Independent Assortment. Mendel's second law, stating that each pair of alleles segregates, or assorts, independently of each other pair during gamete formation; applies when genes for two characters are located on different pairs of homologous chromosomes or when they are far enough apart on the same chromosome to behave as though they are on different chromosomes.

Back

The Law of segregation

Front

Mendel's first law, stating that the two alleles in a pair segregate (separate from each other) into different gametes during gamete formation.

Back

Physically, what are different alleles? (eText Concept 14.1) Different alleles are different DNA sequences found at the same locus on sister chromatids. Different alleles are different particles found in gametes. Different alleles are different phenotypes for a particular character. Different alleles are different DNA sequences found at the same locus on homologous chromosomes. None of the listed responses is correct.

Front

Different alleles are different DNA sequences found at the same locus on homologous chromosomes.

Back

Dihybrid Cross

Front

A cross between two organisms that are each heterozygous for both of the characters being followed (or the self-pollination of a plant that is heterozygous for both characters).

Back

F1 generation

Front

The first filial, hybrid (heterozygous) offspring arising from a parental (P generation) cross.

Back

Concept 14.2 The laws of probability govern Mendelian Inheritance

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...

Back

Homologous pairs of chromosomes often _____. (eText Concept 14.1) carry different genes for different traits differ in length contain different alleles are not both present in diploid somatic cells are paired up in the G2 phase of the cell cycle

Front

contain different alleles

Back

Character

Front

An observable heritable feature that may vary among individuals.

Back

Dihybrids

Front

An organism that is heterozygous with respect to two genes of interest. All the offspring from a cross between parents doubly homozygous for different alleles are dihybrids. For example, parents of genotypes AABB and aabb produce a dihybrid of genotype AaBb.

Back

Concept Check 14.1 Draw It. Pea Plants heterozygous for flower position and stem length (AaTt) are allowed to self pollinate, and 400 of the resulting seeds are planted. Draw a Punnett square for this cross. How many offspring would be predicted to have terminal flowers and be dwarf? (See Table 14.1)

Front

refer to diagram

Back

hybridization

Front

In genetics, the mating, or crossing, of two true-breeding varieties.

Back

True-Breeding

Front

Referring to organisms that produce offspring of the same variety over many generations of self-pollination.

Back

In Mendel's monohybrid cross of purple-flowered and white-flowered peas, all members of the F1 generation had the _____ phenotype because their genotype was _____ at the flower-color locus. (eText Concept 14.1) white-flowered ... homozygous recessive white-flowered ... heterozygous purple-flowered ... homozygous recessive purple-flowered ... homozygous dominant purple-flowered ... heterozygous

Front

purple-flowered ... heterozygous

Back

Monohybrids

Front

An organism that is heterozygous with respect to a single gene of interest. All the offspring from a cross between parents homozygous for different alleles are monohybrids. For example, parents of genotypes AA and aa produce a monohybrid of genotype Aa.

Back

Concept 14.1 Mendel used the scientific approach to identify two laws of Inheritance

Front

The Law of Segregation The Law of Independent Assortment

Back

Genotype

Front

The genetic makeup, or set of alleles, of an organism.

Back

Assume tall (T) is completely dominant to dwarf (t) in a certain species of plant. If a homozygous dominant individual is crossed with a homozygous dwarf, the offspring will _____. (eText Concept 14.1) all be intermediate in height all be tall be 1/2 tall and 1/2 dwarf be 3/4 tall and 1/4 dwarf all be short

Front

all be tall

Back

Punnett Square

Front

A diagram used in the study of inheritance to show the predicted genotypic results of random fertilization in genetic crosses between individuals of known genotype.

Back

If the two traits that Mendel looked at in his dihybrid cross of smooth yellow peas with wrinkled green peas had been controlled by genes that were located near each other on the same chromosome, then the F2 generation _____. (eText Concept 14.1) would have contained four phenotypes in a 9:3:3:1 ratio would have contained only individuals that were heterozygous at both loci would have deviated from the 9:3:3:1 phenotypic ratio that is predicted by the law of independent assortment would have contained no individuals that were heterozygous at both loci None of the listed responses is correct.

Front

Would have deviated from the 9:3:3:1 phenotypic ratio that is predicted by the law of independent assortment If the two characters are located on the same chromosome, they will not segregate independently.

Back

Testcross

Front

Breeding an organism of unknown genotype with a homozygous recessive individual to determine the unknown genotype. The ratio of phenotypes in the offspring reveals the unknown genotype.

Back

Dominant Allele

Front

An allele that is fully expressed in the phenotype of a heterozygote.

Back

Section 2

(47 cards)

Chromosome Theory of Inheritance

Front

A basic principle in biology stating that genes are located at specific positions (loci) on chromosomes and that the behavior of chromosomes during meiosis accounts for inheritance patterns.

Back

Linkage map

Front

A genetic map based on the frequencies of recombination between markers during crossing over of homologous chromosomes.

Back

Trisomic

Front

Referring to a diploid cell that has three copies of a particular chromosome instead of the normal two.

Back

Wild Type

Front

The phenotype most commonly observed in natural populations; also refers to the individual with that phenotype.

Back

Concept 14.4 Many Human Traits Follow Mendelian Patterns of Inheritance

Front

...

Back

Carriers

Front

In genetics, an individual who is heterozygous at a given genetic locus for a recessively inherited disorder. The heterozygote is generally phenotypically normal for the disorder but can pass on the recessive allele to offspring.

Back

Barr Body

Front

A dense object lying along the inside of the nuclear envelope in cells of female mammals, representing a highly condensed, inactivated X chromosome.

Back

Sickle Cell Disease

Front

A recessively inherited human blood disorder in which a single nucleotide change in the β-globin gene causes hemoglobin to aggregate, changing red blood cell shape and causing multiple symptoms in afflicted individuals.

Back

Genetic Map

Front

An ordered list of genetic loci (genes or other genetic markers) along a chromosome.

Back

Polyploidy

Front

A chromosomal alteration in which the organism possesses more than two complete chromosome sets. It is the result of an accident of cell division.

Back

Duplication

Front

An aberration in chromosome structure due to fusion with a fragment from a homologous chromosome, such taht a portion of a chromosome is duplicated.

Back

Parental Types

Front

An offsprring with a phenotyp that matches one of the true-breeding parental (P generation) phenotypes; also refers to the phenotype itself.

Back

Tay-Sachs Disease

Front

A human genetic disease caused by a recessive allele for a dysfunctional enzyme, leading to accumulation of certain lipids in the brain. Seizures, blindness, and degeneration of motor and mental performance usually become manifest a few months after birth, followed by death within a few years.

Back

Monosomic

Front

Referring to a diploid cell that has only one copy of a particular chromosome instead of the normal two.

Back

Concept 15.1 Mendelian Inheritance has its physical basis in the behavior of chromosomes

Front

...

Back

Quantitative Characters

Front

A heritable feature that varies continuously over a range rather than in an either-or fashion.

Back

Duchenne Muscular Dystrophy

Front

A human genetic disease caused by a sex-linked recessive allele; characterized by progressive weakening and a loss of muscle tissue.

Back

Down Syndrome

Front

A humaan genetic disease usually caused by the presence of an extra chromosome 21; characterized by developmental delays and heart and other defects that are generally treatable or non-life threatening.

Back

Multifactorial

Front

Referring to a phenotypic character that is influenced by multiple genes and environmental factors

Back

Huntington's Disease

Front

A human genetic disease caused by a dominant allele, characterized by uncontrollable body movements and degeneration of the nervous system; usually fatal 10 to 20 years after the onset of symptoms.

Back

Concept 15.3 Linked Genes Tend to be Inherited Together because they are Located near Each Other on the Same Chromosome.

Front

...

Back

Nondisjunction

Front

An error in meiosis or mitosis in which members of a pair of homologous chromosomes or a pair of sister chromatids fail to separate properly from each other.

Back

Deletion

Front

(1) A deficiency in a chromosome resulting from the loss of a fragment through breakage. (2) A mutational loss of one or more nucleotide pairs from a gene.

Back

Pedigree

Front

A diagram of a family tree with conventional symbols, showing the occurrence of heritable characters in parents and offspring over multiple generations.

Back

Crossing Over

Front

The reciprocal exchange of genetic material between nonsister chromatids during prophase I of meiosis.

Back

Norm of Reaction

Front

The range of phenotypes produced by a single genotype, due to environmental influences.

Back

Epistasis

Front

A type of gene interaction in which the phenotypic expression of one gene alters that of another independently inherited gene.

Back

Pleiotropy

Front

The ability of a single gene to have multiple effects.

Back

Genetic Recombination

Front

General term for the production of offspring with combinations of traits that differ from those found in either parent.

Back

Inversion

Front

An aberration in chromosome structure resulting from reattachment of a chromosomal fragment in a reverse orientation to the chromosome from which it originated.

Back

Aneuploidy

Front

A chromosomal aberration in which one or more chromosomes are present in extra copies or are deficient in number.

Back

Concept 15.5 Some Inheritance Patterns are exceptions to Standard Mendelian Inheritance

Front

...

Back

Amniocentesis

Front

A technique associated with prenatal diagnosis in which amniotic fluid is obtained by aspiration from a needle inserted into the uterus. The fluid and the fetal cells it contains are analyzed to detect certain genetic and congenital defects in the fetus.

Back

Translocation

Front

(1) An aberration in chromosome structure resulting from attachment of a chromosomal fragment to a nonhomologous chromosome. (2) During protein synthesis, the third stage in the elongation cycle, when the RNA carrying the growing polypeptide moves from the A site to the P site on the ribosome. (3) The transport of organic nutrients in the phloem of vascular plants.

Back

Concept 15.2 Sex-Linked Genes Exhibit Unique Patterns of Inheritance

Front

...

Back

Polygenic Inheritance

Front

An additive effect of two or more genes on a single phenotypic character.

Back

X-Linked Genes

Front

A gene located on the X chromosome; such genes show a distinctive pattern of inheritance.

Back

Map Units

Front

A unit of measurement of the distance between genes. One map unit is equivalent to a 1% recombination frequency.

Back

Chorionic Villus Sampling (CVS)

Front

A technique associated with prenatal diagnosis in which a small sample of the fetal portion of the placenta is removed for analysis to detect certain genetic and congenital defects in the fetus.

Back

Incomplete dominance

Front

The situation in which the phenotype of heterozygotes is intermediate between the phenotypes of individuals homozygous for either allele.

Back

Hemophilia

Front

A human genetic disease caused by a sex-linked recessive allele resulting in the absence of one or more blood-clotting proteins; characterized by excessive bleeding following injury.

Back

Recombinant Types/Recombinants

Front

An offspring whose phenotype differs from that of the true-breeding P generation parents; also refers to the phenotype itself.

Back

Genomic Imprinting

Front

A phenomenon in which expression of an allele in offspring depends on whether the allele is inherited from the male or female parent.

Back

Sex-Linked Gene

Front

A gene located on either sex chromosome. Most sex-linked genes are on the X chromosome and show distinctive patterns of inheritance; there are very few genes on the Y chromosome.

Back

Cystic Fibrosis

Front

A human genetic disorder caused by a recessive allele for a chloride channel protein; characterized by an excessive secretion of mucus and consequent vulnerability to infection; fatal if untreated.

Back

Codominance

Front

The situation in which the phenotypes of both alleles are exhibited in the heterozygote because both alleles affect the phenotype in separate, distinguishable ways.

Back

Concept 15.4 Alterations of Chromosome Number or Structure Cause Some Genetic Disorders

Front

...

Back