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109 Cards in this Set

  • Front
  • Back
What is thought to be the origin of mitochondria? Of chloroplasts?
Purple bacteria/cyanobacteria
In the gene that affects snail coiling, the ______ is responsible for the phenotype of the offspring.
Mother's genotype
Both parents usually imprint the same gene.
False
What is the molecular mechanism for imprinting a gene?
Methylation
Where is extranuclear DNA located in mammalian cells?
Mitochondria
How many Barr bodies would an individual with a XXY genotype possess?
1
The coat color of calico cats is a result of _____.
X-inactivation
Monoallelic expression is associated with which of the following?
Genomic imprinting
Which of the following is true regarding human mtDNA?
It is around 17,000 bp in length.
It is a circular chromosome.
Multiple copies exist in each mitochondria.
It mostly contains rRNA and tRNA genes.
mtDNA contains all of the genes necessary for the complete function of mitochondrial metabolism.
False
cpDNA contains which of the following types of genes?
rRNA, tRNA, Genes for photosynthetic pathways
Dosage compensation offsets the problems associated with differences in the number of _______ chromosomes in many species.
sex
The inheritance patterns of genetic material that is not contained in the nucleus of the cell is called _______.
extranuclear (or cytoplasmic) inheritance
Heteroplasmy is associated with inheritance patterns involving
mitochondria or chloroplasts
Expression of ______ would inhibit X-inactivation.
TsiX
Where is extra nuclear DNA located in mammalian cells?
Mitochondria
Which of the following does not inactivate an X chromosome?
Drosophila
What gene is most responsible for X-inactivation?
Xist
What is a disease associated with extranuclear inheritance?
LHON
What encodes the toxin paramecin in Paramecium aurelia?
Kappa Particles
The inheritance of leaf pigmentation in the four-o'clock plant Mirabilis jalapa is an example of ____.
Maternal inheritance
A modification that occurs to a nuclear gene that alters gene expression, but not permanently, is called _______ inheritance.
epigenetic
In the Igf-2 allele, which chromosome is imprinted? Which is expressed?
Paternal, paternal
What are some diseases associated with imprinting?
Angelman Syndrome
A chromosomal event that precedes X chromosome inactivation is
Locus specific chromosome pairing
First phase of development:
Formation of body axes
Second phase of development:
Segmentation of the body
Third phase of development:
Determination of structures within segments
Fourth phase of development:
Cell differentiation
Which of the following apply to Hox genes?
Adjacent groups of Hox genes form Hox complexes.
In vertebrates, Hox genes play a key role in the anteroposterior axis.
The coding sequence of Hox genes contains the homeobox.
Knockout genes have been used to determine the function of Hox genes.
The order of hox genes on a chromosome is important for the correct expression along the anteroposterior axis of the body. If a mutation occurs that causes one of these genes to be expressed in an area where expression does not normally occur, the outcome is referred to as a ________________________.
gain-of-function mutation
Mutations of plant homeotic genes can result in which of the following outcomes?
Changes in the sepals
Changes in the petals
Changes in the stamen
Changes in the carpels
The ZZ/ZW chromosomes system in determining the sex of individuals is found in _________.
birds
In ________, the sex of individuals is determined by whether an individual is haploid or diploid.
bees
The temperature of the nest during development determines the sex in ____________.
American Alligators
A population of _______________ consists of males and hermaphrodites.
C.elegans
Pole cells are responsible for forming what structures in an adult organism?
Gametes
Gap genes and pair-rule genes are examples of genes that determine _____.
Formation of body segments
Which of the following provide positional information to the developing organism?
Threshold concentration
Morphogens
Induction
Cell adhesion
The bicoid gene is responsible for the formation of what portion of the Drosophila embryo?
Anterior structures
The bicoid gene has what pattern of inheritance?
Maternal inheritance
In Drosophila embryos the anterior compartment of a segment overlaps with the posterior compartment of a parasegment.
True
A homeotic mutation results in which of the following?
Replacing of one body part with another
Antennapedia in Drosophila is an example of a _________.
Gain of function mutation
Homeodomains _____.
Are the protein domains encoded by homeoboxes
Are part of transcription factors
Bind to the major groove of DNA
Cell lineage diagrams are most easily prepared in which of the following model organisms?
C. elegans
A mutation in which the fate of cell lineages is not synchronized in an organism is called a ____.
Heterochronic mutation
Studies of invertebrate and vertebrate development suggest that there is a universal body plan for animal development.
True
The model organism for the study of plant development is _____.
Arabidopsis thaliana
A mutation in the B genes of Arabidopsis would result in the incorrect formation of what structure?
Flowers
Which of the following genes must be expressed in Drosophila for development into a female fly?
SXL
In humans, what gene determines maleness?
SRY
In humans, an XY individual in which a deletion has inactivated SRY would developmentally be what sex?
Female
Genes that specify the final identity of a body region are called _______.
homeotic
Molecules that convey positional information and promote developmental changes are called _______.
morphogens
The _______ of a morphogen determines its effect on development.
concentration
Skeletal muscle cell development is controlled by _______ proteins.
myogenic bHLH
The ABC model explains the process of _______.
flower development
If the lin-14 gene product persists for too long, this causes the worm to have
More cells
The scientific basis for studying mutant worms exhibiting a defective egg-laying phenotype was that
Some worms with this phenotype may have a heterochronic mutation.
In the following sequence of DNA, the italicized base has been mutated. What type of mutation is this?
5' - G A T C T C C G A A T T - 3' original strand
5' - G A T C T C C C A A T T - 3' mutated strand
Transversion
The Bar mutation in Drosophila, in which affected flies have a very narrow eye, is an example of a ______ - level mutation.
Chromosome
Anticipation is associated with which of the following?
Trinucleotide repeat expansions
Which of the following codons would typically be repeated in a trinucleotide expansion repeat region?
CAG
Translocations and inversions may cause which of the following?
Position effect
A translocation that moves a gene from an area of euchromatin to heterochromatin would typically cause a(n) _______ in the expression of the gene.
Reduction
Which of the following is not an example of a spontaneous mutation?
UV light induced thymine dimers
The results of the replica plating experiments by the Lederbergs supported which of the following theories?
Random mutation theory
After screening a colony of bacteria for a given gene, you discover 100 mutant colonies out of 3 million total colonies. What is the mutation frequency for this gene in the population?
3.3 x 10-5
Which of the following is correct regarding the rate of mutation?
Rates of mutation per cell generation typically range from 10-5 to 10-9
The conversion of cytosine to uracil in DNA is an example of _____.
Deamination
The complete loss of either a guanine or adenine from DNA is an example of _____.
Depurination
Which of the following are examples of suppressor mutations?
An intragenic mutation that restores protein structure
A temporary change in the bonding arrangements of a nitrogenous base is called ______.
A tautomeric shift
The first environmental agent shown to induce mutation was _____.
X-rays
Which of the following is an example of a base analog?
5BU
Uses enzymes called the DNA-N-glycolases.
Base excision repair
Is responsible for repairing damage from UV radiation.
Nucleotide excision repair
Photolyase in yeast is an enzyme associated with
Direct repair
Utilizes MutL, MutH, and MutS proteins in E. coli.
Mismatch repair
Often leads to deletion in chromosome sequence.
Nonhomologous end joining (NHEJ)
Identifies daughter strands by methylation.
Mismatch repair
In the nucleotide excision repair system, which of the following proteins is responsible for recognizing a thymine dimer to be repaired?
UvrAB
The Ames test may be used to determine if an agent is a mutagen.
True
A change in the chromosome number is called a point mutation.
False
An individual that is a genetic mosaic would be the result of a______mutation.
somatic cell
Recognizes double stranded breaks and unwinds DNA.
RecBCD
Binds to single stranded DNA and promotes strand invasion.
RecA
Promotes branch migration
RuvAB
Is an endonuclease.
RuvC
During the lysogenic stage of the lambda phage lifecycle, lambda DNA inserts into the genome using a site specific recombinational event. Which of the following is not necessary for this to occur?
UV light
Requires transposase to transpose
composite transposon
Requires reverse transcriptase
viral like retroelement
Contains direct repeats
composite transposon and viral like retroelement
Contains inverted repeats
composite transposon
Has long terminal repeats
viral like retroelement
Has an integrase gene
viral like retroelement
Where does crossing over occur?
Prophase of Meiosis I
Which of the following most likely accounts for the majority of the recombination events during both DNA repair and meiosis?
Double-break model
D-Loop formation is associated with _______
the double-break model
Bacteriophage l inserts into a bacterial chromosome using which of the following?
DNA gap repair
Which of the following processes accounts for the tremendous variation in antibody structure?
Site-specific recombination
Which of the following domain types is unique to the heavy chain of the polypeptide?
D
RAG1 and RAG2 proteins are associated with which of the following?
Site-specific recombination in antibodies
Which of the following genes was mobile in McClintock's experiments with mutable sites in corn?
Ds
The type of transposition in which the number of transposons increases in the genome is called ______.
Replicative transposition
Insertion sequences can be identified by which of the following?
presence of integrase
Which of the following is technically not part of the genetic information of a transposable element?
Direct repeats
A heteroduplex is a DNA double helix that contains mismatches.
True