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71 Cards in this Set

  • Front
  • Back
A type of genetic mapping used with Hfr and F- strains of bacteria is called ____________
time of entry
A plasmid that confers resistance to multiple antibiotics by recombination with corresponding cassettes is called a __________
d. Integron
3. The sequence present in a tRNA molecule that undergoes base pairing with the corresponding codon in the mRNA is the __________.
anticodon
4. Another term for coding sequence in DNA is ________
open reading frame
DNA replication from the origin of replication is
bidirectional & semiconservative
A complex of four histone molecules, each present in two copies, wrapped by two turns of DNA is called a _____________.
a. Nucleosome
A chromosome with its centromere in the middle is
b. metacentric
Familial Down syndrome may result from which of the following chromosomal abnormalities?
heterozygosity for rob(14:21) [Robertsonian translocation]
The master sex-determining gene SRY that codes for the testis-determining factor, resides on
e. in the short arm of the Y chromosome, but out of pseudoautosomal region.
Regions of the chromosome with very few functional genes are called
c. heterochromatin.
11. In most eukaryotic genomes, the DNA consists of
d. unique, and middle and highly repetitive DNA
12. Individuals whose karyotypes are 47 XXY are phenotypically ___________
Male
In DNA sequencing, dideoxyribonucleotides
act as chain terminators
Gene conversion results from
crossing over
A megabase of DNA consists of
10 6 bp
16. A circular DNA molecule that is not over-twisted in either direction is said to be
relaxed.
17. The consequences of gene conversion are observed in the following fungal tetrad segregation ratios:
b and c
RNA synthesis on a DNA template is called __________.
transcription
At the molecular level, crossing over begins with a double strand break, strand invasion and the formation of heteroduplexes which may lead to which of the following
All of the above
In log of odds genetic mapping in humans the results are given as map distance between a molecular marker and a genetic trait in :
a. Recombination of flanking markers
b. Recombination and the conversion of wild-type to mutant alleles (or vis versa)
c. Gene conversion in the absence of recombination
d. All of the above
e. None of the above
all the above
20. In log of odds genetic mapping in humans the results are given as map distance between a molecular marker and a genetic trait in :
a curve showing how the lod score changes as a function of recombination frequency
An exonuclease is an enzyme that can
remove a terminal nucleotide in a polynucleotide chain.
Which of the following correctly describe an individual with Turner syndrome who is monosomic for the X chromosome

a. euploid
b. 45, X0
c. aneuploid
d. a&b
e. b &c
b &c
The portion of the tRNA where the amino acid is conjugated.
3’ acceptor arm
Which processes, are coupled in prokaryotes?
Transcription and translation
In mRNA translation, Wobble refers to the ability of
A single aa-tRNA anticodon to bind to two or more synonymous codons.
Heritable change in gene expression that is associated with chemical modification of DNA or chromatin but not with a change in DNA sequence are called __________.
Epigenetic
The DNA binding site for prokaryotic RNA polymerase
Promoter
Regions at the 5’ and 3’ end of eukaryotic mRNAs that are not translated into protein.
Untranslated region
Bacterial operons which are transcribed unless they are specifically turned off are said to be regulated by
Repressible transcription
A method for treatment of disease by means of DNA rather than proteins or other pharmaceuticals is called ____________.
Gene therapy
The process of assembling of two DNA molecules by in vitro manipulation is _____________.
Recombinant DNA technology
A gene whose expression can readily be monitored is a ___________
Reporter gene
Study of the DNA sequence, organization, function, and evolution of genomes
Genomics
A nucleotide substitution in a codon that changes a single amino acid is a ____________.
Nonsynonymous mutation
The presence of two genetically different mitochondria within the same cell is an example of
heteroplasmy
__________ is a phenomenon in normal mammalian cells in culture whereby cells cease to grow and divide when they are in close physical proximity.
Contact inhibition
Loss of the presence of the wildtype allele, or loss of its function, in a heterozygous cell, enabling the phenotype of a recessive mutant allele to be expressed, is termed ___________.
Loss of heterozygosity
A class of mutations which result in multiple contiguous amino acid differences in proteins is likely :
frameshift.
In a precancerous condition, a new mutation in the cell cycle checkpoint protein p53 will allow which of the following to accumulate in daughter cells_________

a. Deletions
b. Translocations
c. Gene or chromosome amplification
All the above
Which of the following clusters of terms describes eukaryotic enhancers:
cis-acting, variable position
In the early stages of the cell cycle, progression from one phase to the next is controlled by the ______________
cyclin-CDK complexes.
A population of 1  108 bacterial cells undergoes one round of DNA replication and cell division. If a mutation rate of a gene is 1  10-5per replication, the expected number of mutant cells after cell division is
10^3
1) The maximum recombination frequency that may be measured between two genes in a single mapping experiment is
50%
An allele is
an alternate form of a gene.
4) Apply the product law to a coin-flip situation. What is the probability that on three flips of a coin, heads will occur on all three times?
1/8
5) The fundamental Mendelian process which involves the separation of alleles at the same locus on homologous chromosomes would be called ________
segregation
6) With codominance, a likely phenotypic ratio resulting from a monohybrid cross would be
1:2:1
7) If a typical somatic cell has 24 chromosomes, how many chromosomes are expected in each gamete of that organism?
12
In tigers, a recessive allele causes a white tiger (virtual absence of fur pigmentation). If two phenotypically normal tigers are mated and produce a white offspring, what is the probability that these tigers will have another white offspring?
1/4
Tight curly hair is caused by a dominant gene in humans. This trait is rare among northern Europeans. If a curly-haired northern European marries a person with straight hair, what proportion of their offspring would be expected to have curly hair?
1/2 curly
11) A condition in which one gene pair masks the expression of a non-allelic gene pair is _____.
epistasis
12) The physical or biochemical expression of the genotype is called the ____________.
phenotype
13) All of the following are genetic markers that can be used to follow a trait between generations except ___________
complementation
14) Hemizygosity would most likely be associated with which of the following?
X-linked inheritance
15) Hemophilia is caused by several genetic factors; one, a sex-linked recessive gene, is the subject of this problem. Assume that a man with hemophilia marries a normal woman whose father had hemophilia. What is the probability that their first child will have hemophilia? [Hint: in this problem you must include the probability of having a son in your computation of the final probability.]
1/4
16) A man who carries an X-linked allele (gene) will pass it on to
all of his daughters.
17) Assuming independent assortment in a test cross between an individual who is double heterozygous and a tester strain that is homozygous recessive for both traits, the proportion of offspring who are double homozygous recessive are:
¼
The chromatids in a pair of chromosomes are held together at a specific region of the chromosome called the
centromere.
19) A cell with a nucleus containing only one set of chromosomes, consisting of one member of each homologous pair, is

A. diploid B. haploid C. somatic cell D. gamete
E. both B and D
20) The mitotic stage in which the chromosomes condense, the nucleoli disappear, and the mitotic spindle forms is known as
prophase
Parents heterozygous for a recessive allele are called:
Carriers
Meiosis consists of how many successive nuclear divisions?
two
23) The centromeres of sister chromatids uncouple and chromatids separate in which meiotic phase?
. anaphase II
24) When three genes are close together, the frequency at which double crossovers occur is usually reduced by __________________.
Interference
25) With respect to chromosome number, the first division in meiosis is known as the ______ division.
reductional
Which of the following statements about restriction enzymes is false?
B. Unlike many morphological phenotypes restriction fragment length polymorphisms are dominant.
Which one of the following statements about sex determination in chickens is false?
♂ are hemizygous for the sex chromosome
28) In a mating between individuals with the genotypes IAIO x IOIO, what percentage of the offspring are expected to have the O blood type?
50%
Genes that are found on the same chromosome are said to be ____________.
linked
In the universal genetic code, minimum number of bases needed to specify one of the twenty common amino acid is:
3