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Concept explainers
To determine:
The way by which the approach of releasing laboratory-reared insects that are homozygous for several translocations will work and mentioning the insects which will be sterile.
Introduction:
Translocation refers to a specific type of chromosomal rearrangement. In the case of translocation, two non-homologous chromosomes exchange different parts with each other. The genes are present in the gametes of the translocation homozygotes, but the genes are present in a haphazard fashion. For example; a gene is present on chromosome 6, and another gene 'y' is present on chromosome no. 9 in a normal cell. These two genes undergo a reciprocal translocation. So, in the translocation homozygote, gene 'x' will be present on chromosome 9, and gene 'y' will be present on chromosome no. 6. This cell has both the genes ‘x’ and ‘y’ (on different chromosomes).
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Chapter 12 Solutions
Genetics: From Genes to Genomes, 5th edition
- In corn, male sterility is controlled by maternal cytoplasmic elements. This phenotype renders the male part of the corn plants (i.e the tassel) unable to produce fertile pollen; the female parts, however, remain receptive to pollination by pollen from male fertile corn plants. However, the presence of a nuclear fertility restorer gene F restores fertility to male sterile lines Using the cardboard chips, simulate the crosses indicated below. Give the genotypes and phenotypes of the offsprings in each cross, and properly label the nucleus and the cytoplasm of each individual in the cross Legend male sterile cytoplasm Male fertile cytoplasm FF nucleus Ff nucleus ff nucleus A. Male sterile female x FF male Explain the phenotype of the offspring B. Male sterile female x Ff male Explain the phenotype of the offspringarrow_forwardBecause of the relatively high frequency of meiotic errors that lead to developmental abnormalities in humans, many research efforts have focused on identifying correlations between error frequency and chromosome morphology and behavior. Tease et al. (2002) studied human fetal oocytes of chromosomes 21, 18, and 13 using an immunocytological approach that allowed a direct estimate of the frequency and position of meiotic recombination. Below is a summary of information [modified from Tease et al. (2002)] that compares recombination frequency with the frequency of trisomy for chromosomes 21, 18, and 13. (Note: You may want to read appropriate portions of Chapter 8 for descriptions of these trisomic conditions.) Trisomic Mean Recombination Frequency Live-born Frequency Chromosome 21 1.23 1/700 Chromosome 18 2.36 1/3000–1/8000 Chromosome 13 2.50 1/5000–1/19,000 (a) What conclusions can be drawn from these data in terms of recombination and nondisjunction frequencies? How might…arrow_forwardFemales heterozygous for the recessive second chromosome mutations px, sp, and cn are mated to a male homozygous for all three mutations. The offspring are as follows: Must show all work 1.) What gene is in the middle? and what are the map distances between the genes in centimorgans? 2.) What is the interference?arrow_forward
- Wild-type strains of the haploid fungus Neurospora canmake their own tryptophan. An abnormal allele td renders the fungus incapable of making its own tryptophan.An individual of genotype td grows only when its medium supplies tryptophan. The allele su assorts independently of td; its only known effect is to suppress the tdphenotype. Therefore, strains carrying both td and su donot require tryptophan for growth.a. If a td ; su strain is crossed with a genotypically wildtype strain, what genotypes are expected in the progenyand in what proportions?b. What will be the ratio of tryptophan-dependent totryptophan-independent progeny in the cross of part a?arrow_forwardFemales of wild-type Strain A and males of mutant Strain B, as well as females of mutant Strain B and males of wild-type Strain A, make reciprocal crosses. Explain why reciprocal crosses are needed in genetics experiments involving Drosophila fruit flies.arrow_forwardn corn, male sterility is controlled by maternal cytoplasmic elements. This phenotype renders the male part of the corn plants (i.e the tassel) unable to produce fertile pollen; the female parts, however, remain receptive to pollination by pollen from male fertile corn plants. However, the presence of a nuclear fertility restorer gene F restores fertility to male sterile lines Using the cardboard chips, simulate the crosses indicated below. Give the genotypes and phenotypes of the offsprings in each cross, and properly label the nucleus and the cytoplasm each individual in the cross Legend male sterile cytoplasm Male fertile cytoplasm FF nucleus Ff nucleus ff nucleus A. Male sterile female x FF male Explain the phenotype of the offspring B. Male sterile female x Ff male Explain the phenotype of the offspringarrow_forward
- Consider the first category of test-cross offspring shown in figure 8.2 (+b, LS). Consider also that the parents of the heterozygous female flies in the test cross had the following genotypes: bb, SS, and +, LL. A. What would be the physical phenotype of these flies? B. If PC was conducted with the DNA of one of these flies using the primers for the molecular marker, what would be the appearance of the bands on an electrophoresis gel with the PC products? C. If the gene for black body and the locus for the molecular marker (L long or S short) were unlinked, what proportion of the test-cross progeny would be black flies that are heterozygous for the molecular marker? What proportion would be flies with normal body color, which are homozygous for one form of the molecular marker? D. If the gene for black body and the locus for the molecular marker were linked, how would the proportion of flies be different?arrow_forwardA PI in your facility has finished working with his transgenic line of mice and would like you to cryopreserve embryos (freeze them in liquid nitrogen) so that he can keep them for later experimentation without paying the extra cost of a breeding colony. Which of the following steps do you take? Select all that apply: a) Use the van der Lee/Boot and Whitten effect to time mate your females. b) Superovulate your females by injecting with PMSG and hCG. c) Breed the mice with a vasectomized male. d) Collect ova from the ampulla the day you find a plug. e) Collect blastocysts from the uterus 3 days after finding a plug.arrow_forwardExplain the following: a- No parental type is produced during gametogenesis? b- A dominant wild type produced a sign spot in Drosophila? c- 9:7 phenotypic ratio is produced in dihybrid cross? d- 50% parental type gametes were produced during gametogenesis? e- All recombinant gametes were produced during gametogenesis?arrow_forward
- Name the type of translocations and explain their mechanism of occurrence.arrow_forwardIn the past, the IOC has employed two genetic sex- determination tests. The Barr body test screens for the presence of two X chromosomes. In XX somatic cells, one copy of the X chromosome condenses into a largely inactive structure called a Barr body, which can be seen using a light microscope. In more recent years, a polymerase chain reaction-based screen has been used to amplify the DNA sequence of the SRY gene, which is found only on the Y chromosome. Based on their karyotypes, what would be the outcome of these two tests for each of the four individuals? Drag the labels to indicate the presence or absence of a Barr body and the SRY gene sequence.arrow_forwardIn com, male sterility is controlled by maternal cytoplasmic elements. However, the presence of a nuclear fertility restorer gene (F_) restores fertility to male sterile lines. a. What are the crosses male sterile female x FF male? Give the genotypes and phenotypes of the offspring in each cross. Explain.arrow_forward
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