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You and a colleague are working on a rare Peruvian llama that appears to be susceptible to diabetes, a disease related to insulin function. Your colleague has established a somatic-cell hybrid panel, and you would like to figure out to which llama chromosome the gene that encodes the llama insulin receptor maps. You also have an assay that allows you to detect which of the somatic-cell lines can produce the insulin receptor. You assay the colleague's somatic-cell hybrid panel and get the following results. Which of the 74 llama chromosomes is the gene on?  Line #  Llama chromosomes  Assay 17,10,15,29,41,55,6824,8,16,31,44,56,7039,12,18,52,54,61,73+41,8,13,22,33,45,5952,11,14,18,23,49,62+65,12,15,24,35,47,6373,17,21,32,43,58,7287,21,25,36,53,6491,3,9,28,37,48,651013,22,27,38,50,66,19114,6,12,18,20,40,67+122,16,26,34,51,691310,14,17,39,46,57,74145,11,19,30,42,60,71\begin{array} { l l l } \text { Line \# } & \text { Llama chromosomes } & \text { Assay } \\\hline 1 & 7,10,15,29,41,55,68 & - \\2 & 4,8,16,31,44,56,70 & - \\3 & 9,12,18,52,54,61,73 & + \\4 & 1,8,13,22,33,45,59 & - \\5 & 2,11,14,18,23,49,62 & + \\6 & 5,12,15,24,35,47,63 & - \\7 & 3,17,21,32,43,58,72 & - \\8 & 7,21,25,36,53,64 & - \\9 & 1,3,9,28,37,48,65 & - \\10 & 13,22,27,38,50,66,19 & - \\11 & 4,6,12,18,20,40,67 & + \\12 & 2,16,26,34,51,69 & - \\13 & 10,14,17,39,46,57,74 & - \\14 & 5,11,19,30,42,60,71 & -\end{array}


A) 55
B) 7
C) 41
D) 68
E) 18

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In soreflies (a hypothetical insect) , the dominant allele, L, is responsible for resistance to a common insecticide called Loritol. Another dominant allele, M, is responsible for the ability of soreflies to sing like birds. A true-breeding mute, Loritol-resistant sorefly was mated to a true-breeding singing, Loritol-sensitive sorefly, and the singing, Loritol-resistant female progeny were test-crossed with true-breeding wild-type (i.e., mute, Loritol-sensitive) males. Of the 400 total progeny produced, 117 were mute and Loritol-resistant, 114 could sing and were Loritol-sensitive, 83 could sing and were Loritol-resistant, and 86 were mute and Loritol-sensitive. What will be the results of a chi-square test for independent assortment?


A) 9.70 with three degrees of freedom
B) 4.63 with three degrees of freedom
C) 6.48 with four degrees of freedom
D) 2.54 with one degree of freedom
E) Because there are four classes of offspring, the genes must be assorting independently.

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What does lod stand for?


A) linkage over DNA
B) linkage of dihybrids
C) long overall distances (with respect to map distances)
D) linker of DNA
E) logarithm of odds

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Linked genes:


A) assort randomly.
B) cannot cross over and recombine.
C) are allelic.
D) co-segregate.
E) will segregate independently.

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What is a major difference in using lod-score analysis compared to using association studies in determining gene locations in humans?


A) Lod-score analysis relies on family or pedigree data, while association studies use population data.
B) Lod-score analysis requires that the loci being mapped must be on different chromosome arms, while association studies can map genes on different chromosomes.
C) Association studies compare genotypes between parents and their children, while lod-score analysis compares genotypes between siblings of the same family.
D) Lod-score analysis requires isolated human populations, while association studies require very large family pedigrees.
E) Lod-score analysis requires a large number of genes with multiple alleles, while association studies can use genes that have only two alleles.

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Use the following to answer questions : You just bought two black guinea pigs, one male and one female, of the same genotype from the pet store that are known to be heterozygous (Bb) . You also know that black fur (BB) is dominant over white fur (bb) and that a lethal recessive allele is located only 1 m.u. away from the recessive b allele, and your animals are both heterozygous for this gene also. -You decide to start raising your own guinea pigs, but after mating these animals several times, you discover they produce only black offspring among the first 12 progeny. How would you best explain this result?


A) The B locus is on the X chromosome, so it can never produce a white phenotype.
B) The B allele is actually codominant with the b allele, so a white phenotype cannot be produced.
C) The recessive l allele is in tight coupling linkage with the b allele, so almost all of the bb offspring will also be ll and thus die before they can be observed.
D) The dominant L allele is in tight repulsion linkage with the B allele, so it will be impossible to produce the Bb genotype that would express the white phenotype.
E) Normally, it would be expected that 25% of the offspring would be white, but in this case, random deviations from the expected resulted in no white offspring.

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Assume that you discover a new human gene that you believe is located on the Y chromosome although not in the region (pseudoautosomal) of the Y that is homologous with part of the X chromosome. How would you map this gene with respect to the other genes on the Y chromosome?

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To map the new gene with respect to the ...

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If the recombination frequency between genes (A) and (B) is 5.3%, what is the distance between the genes in map units on the linkage map?


A) 53 m.u.
B) 5.3 m.u.
C) 0.53 m.u.
D) 10.6 m.u.
E) 25 m.u.

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Linkage disequilibrium is defined by which of the following?


A) positions in the genome where people vary by a single nucleotide base
B) the probability that two genes are linked
C) the nonrandom association between alleles in a haplotype
D) the occurrence of two alleles in the repulsion configuration
E) crossing over that occurs between two genes that are located close to each other

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What major contribution did Barbara McClintock and Harriet Creighton make to the study of recombination?


A) Genetic recombination of alleles is associated with physical exchange between chromosomes.
B) Genes are located on chromosomes and the map distance between them could often be measured by the number of nucleotides in the DNA.
C) Determining map distances in humans could be done by using pedigrees and calculating lod scores.
D) Association studies allow genes that have no obvious phenotype to be accurately mapped.
E) Crossing over does not occur in male Drosophila, so there is no genetic recombination.

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A double heterozygote for two linked genes in the mouse is test-crossed by crossing it to a homozygous recessive parent. In the offspring, the two parental classes appear in a frequency of 45% each, and the two recombinant classes appear in a frequency of 5% each. What is the distance in map units between the two genes?


A) 45 m.u.
B) 22.5 m.u.
C) 10 m.u.
D) 5 m.u.
E) 2.5 m.u.

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Genetic distances within a given linkage group: (Select all that apply.)


A) cannot exceed 100 m.u.
B) are dependent on crossover frequencies between paired, nonsister chromatids.
C) can be measured in centiMorgans or map units.
D) cannot be determined.
E) can only be determined by physical mapping techniques.

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A testcross includes:


A) one parent who is homozygous recessive for one gene pair and a second parent who is homozygous recessive for a second gene pair.
B) one parent who is homozygous dominant for one or more genes and a second parent who is homozygous recessive for these same genes.
C) two parents who are both heterozygous for two or more genes.
D) one parent who shows the dominant phenotype for one or more genes and a second parent who is homozygous recessive for these genes.
E) one parent who shows the recessive phenotype for one or more genes and a second parent who is homozygous dominant for these genes.

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The results of linkage analysis for DNA marker A and the p53 gene are shown below. What is the best estimate for the approximate genetic distance between marker A and the p53 gene in humans?  Recombination values (m.u.)  1510203040 lod score 2.132.543.144.104.963.22\begin{array} { c c c c c c c } \text { Recombination values (m.u.) } & 1 & 5 & 10 & 20 & 30 & 40 \\\text { lod score } & 2.13 & 2.54 & 3.14 & 4.10 & 4.96 & 3.22\end{array}


A) 1 m.u.
B) 5 m.u.
C) 10 m.u.
D) 20 m.u.
E) 30 m.u.

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You are examining the following human pedigree and want to determine if the rare dominant disease allele (D) is linked to a specific DNA sequence location you are using as a molecular marker. Parental and progeny genotypes and phenotypes are indicated. Note that the father is a dihybrid at both loci, but the mother is homozygous at both loci. There is complete penetrance of the trait and a linkage phase of D-R1/d-R2 in the father. Assuming that the marker and the gene are linked, what is the best estimate of the map distance between the two loci? You are examining the following human pedigree and want to determine if the rare dominant disease allele (D)  is linked to a specific DNA sequence location you are using as a molecular marker. Parental and progeny genotypes and phenotypes are indicated. Note that the father is a dihybrid at both loci, but the mother is homozygous at both loci. There is complete penetrance of the trait and a linkage phase of D-R1/d-R2 in the father. Assuming that the marker and the gene are linked, what is the best estimate of the map distance between the two loci?   A)  12 m.u. B)  50 m.u. C)  16 m.u. D)  5 m.u. E)  25 m.u.


A) 12 m.u.
B) 50 m.u.
C) 16 m.u.
D) 5 m.u.
E) 25 m.u.

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In using somatic-cell hybridization experiments, a human gene was found to be located on chromosome 6. However, when lod-score analysis was done to detect linkage between this gene and a DNA marker locus also known to be on chromosome 6, no linkage could be found between the marker locus and the gene. What is the MOST likely explanation for this result?


A) Somatic-cell hybridization experiments are not very accurate, and the gene may be on chromosome 5 or chromosome 7 instead of chromosome 6.
B) Too few recombinants could be found to indicate linkage in the lod-score analysis.
C) A lod-score analysis cannot be used when a DNA marker locus needs to mapped with respect to a gene locus.
D) The gene and the DNA marker locus are so far apart on chromosome 6 that they assort independently.
E) There were probably too few double-crossover events occurring between the two loci, so the lod score could not be determined accurately.

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A genetic map shows which of the following?


A) the distance in numbers of nucleotides between two genes
B) the number of genes on each of the chromosomes of a species
C) the linear order of genes on a chromosome
D) the location of chromosomes in the nucleus when they line up at metaphase during mitosis
E) the location of double crossovers that occur between two genes

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A low coefficient of coincidence indicates that:


A) far fewer double-crossover recombinant progeny were recovered from a testcross than would be expected from the map distances of the genes involved.
B) crossing over has been enhanced for genes that are located near the centromere of chromosomes because there is less interference of one crossover on the occurrence of a second crossover event.
C) single-crossover recombinant classes in the progeny have been increased because the genes involved produce lethal phenotypes when in parental gene combinations.
D) there is a large map distance between one of the outside genes in the heterozygous parent and the middle gene, while there is a short map distance between the middle gene and the other outside gene.
E) the physical distance between two genes is very short compared with the genetic map distance between these two genes.

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Linked genes always exhibit:


A) phenotypes that are similar.
B) recombination frequencies of less than 50%.
C) homozygosity when involved in a testcross.
D) a greater number of recombinant offspring than parental offspring when involved in a testcross.
E) a lack of recombinant offspring when a heterozygous parent is involved in a testcross.

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Consider the following three-point (trihybrid) testcross: Consider the following three-point (trihybrid)  testcross:   Calculate the number of double crossovers you would expect to observe if 1000 progeny result from this testcross assuming a coefficient of coincidence of 0.25. A)  about 14 B)  about 26 C)  about 10 D)  about 4 E)  none because of crossover interference Calculate the number of double crossovers you would expect to observe if 1000 progeny result from this testcross assuming a coefficient of coincidence of 0.25.


A) about 14
B) about 26
C) about 10
D) about 4
E) none because of crossover interference

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