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A: Hi dear, here's your answer what you want.can you please give me a like for this answer. Hypomorph…
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A: No, the mechanism of recombination of unlinked genes does not require crossing-over.
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Q: What is homologous recombination?
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Genetic Recombination
Recombination is crucial to this process because it allows genes to be reassorted into diverse combinations. Genetic recombination is the process of combining genetic components from two different origins into a single unit. In prokaryotes, genetic recombination takes place by the unilateral transfer of deoxyribonucleic acid. It includes transduction, transformation, and conjugation. The genetic exchange occurring between homologous deoxyribonucleic acid sequences (DNA) from two different sources is termed general recombination. For this to happen, an identical sequence of the two recombining molecules is required. The process of genetic exchange which occurs in eukaryotes during sexual reproduction such as meiosis is an example of this type of genetic recombination.
Microbial Genetics
Genes are the functional units of heredity. They transfer characteristic information from parents to the offspring.
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- Homozyogous wild type male Drosophila PPQQRRSSTTUUVV (all linked) are irradiated to induce the formation of chromosomal deletions and then mated with homozygous recessive females. In several of these matings a unique pattern of pseudodominance could be correlated with the loss of specific polytene chromosome bands, as shown in the table... Cross Chromosomal Bands Deleted Pattern of Pseudodominance PqRs TuV 1 2 3 4 5 5-6 1-2 3-5 6-8 1-3 PQRSTUV PqrSTUV PQRSTUV pQrSTUV In which chromosomal band is gene R located? A. 3 OB. 4 OC. 2 D.8 O E. none of these answers are correctIn Drosophila flies, the allele b gives a black body, and the allele b+ gives brown, the wild-typephenotype. The allele wx of a separate gene gives waxy wings, and wx+ gives non-waxy. The allele cn ofa third gene gives cinnabar eyes, and cn+ gives red. A female heterozygous for these three genes istestcrossed, and 745 progenies are produced which are phenotypically classified as follows:5 b+ wx+ cn+4 b wx cn53 b+ wx cn 49 b wx+ cn+287 b+ wx+ cn279 b wx cn+ 33 b+ wx cn+35 b wx+ cn Make a linkage map of the three genes. Compute for interference and explain what the derived valuemeans. Show complete solutions to support your answers.Drosophila P elements were discovered because ofa phenomenon called hybrid dysgenesis—sterilityof particular hybrid progeny. When scientists in the1970s crossed their D. melanogaster laboratorystrains to flies of the same species obtained fromnatural environments outside the lab, they observeda remarkable result: The progeny of the crosseswere sterile, but only when outside males werecrossed with lab strain females. Progeny resultingfrom crosses of outside females with lab maleswere perfectly normal.DNA analysis revealed that while the genomesof the outside flies contain P elements, the lab flygenomes have none. Apparently, P elements spreadthroughout the wild population of D. melanogasterafter the capture of the originators of present-daylaboratory strains over 100 years ago.a. The hybrid progeny are sterile because their germline cells have a high rate of mutation and chromosomal rearrangement (dysgenesis) caused by highrates of P element mobilization. Explain howP element movement…
- The a, b, and c loci are all on different chromosomesin yeast. When a b+ yeast were crossed to a+ b yeastand the resultant tetrads analyzed, it was found thatthe number of nonparental ditype tetrads was equal tothe number of parental ditypes, but there were no tetratype asci at all. On the other hand, many tetratypeasci were seen in the tetrads formed after a c+ wascrossed with a+ c, and after b c+ was crossed withb+ c. Explain these results.A Drosophila male is heterozygous for a reciprocaltranslocation between an autosome and the Y chromosome. The part of the autosome now present onthe Y chromosome contains the dominant mutationLyra (shortened wings); the other (normal) copyof the same autosome is Lyra+. This male is nowmated with a true-breeding, wild-type female. Whatkinds of progeny would be obtained, and in whatproportions?In Drosophila, a heterozygous female for the X-linkedrecessive traits a, b, and c was crossed to a male that phenotypically expressed a, b, and c. The offspring occurred inthe following phenotypic ratios.+ b c 460a + + 450a b c 32+ + + 38a + c 11+ b + 9 No other phenotypes were observed.(a) What progeny phenotypes are missing? Why?
- of der(X) der(22) 22 der(X) 22 der(X) 22 First row is mother, second row is first daughter, third row is second daughter. Phenotype in first daughter was much more severe than second daughter. Give best explanation: O Inactivation in second daughter spread to the extra chromosome 22 segment O Having 45 chromosomes always gives a more severe phenotype than 46 chromosomes Pattern of inactivation in other tissues, including brain might differ, giving functional 22q monosomy O The presence of the third X in the second daughter decreases effect of genetic abnormality O irst daughter has a Turner-like syndrome, which explains severity --------- ---------- ---------- ------------ ---------. ------------- ------------ OO ixYou are given a Drosophila female that looks wild-type but is heterozygous for mutations intan body (t), miniature wings (m), and white eyes (w). You test cross this female with a tanbodied, miniature winged, and white-eyed homozygous mutant male, and you obtain thefollowing 1400 progeny: Phenotype : number+ + + : 608t m w : 516+ m w : 2t + + : 6+ m + : 39t + w : 46+ + w : 81t m + : 102 Calculate the distance between each pair t-m, m-w, and t-w only using the number ofrecombinants between them (i.e. ignoring the gene in the middle). Draw a linear map with thedistances between genes.In Drosophila, a heterozygous female for the X-linkedrecessive traits a, b, and c was crossed to a male that phenotypically expressed a, b, and c. The offspring occurred inthe following phenotypic ratios.+ b c 460a + + 450a b c 32+ + + 38a + c 11+ b + 9 No other phenotypes were observed.(a) What is the genotypic arrangement of the alleles ofthese genes on the X chromosome of the female?
- In Drosophila, a heterozygous female for the X-linkedrecessive traits a, b, and c was crossed to a male that phenotypically expressed a, b, and c. The offspring occurred inthe following phenotypic ratios.+ b c 460a + + 450a b c 32+ + + 38a + c 11+ b + 9 No other phenotypes were observed.(a) Determine the correct sequence and construct amap of these genes on the X chromosome ?The Drosophila chromosome 4 is extremely small;virtually no recombination occurs between genes onthis chromosome. You have available three differentlymarked chromosome 4s: one has a recessive allele ofthe gene eyeless (ey), causing very small eyes; one hasa recessive allele of the cubitus interruptus (ci) gene,which causes disruptions in the veins on the wings;and the third carries recessive alleles of both genes.Drosophila adults can survive with two or three, butnot with one or four, copies of chromosome 4.a. How could you use these three chromosomes tofind Drosophila mutants with defective meiosescausing an elevated rate of nondisjunction?b. Would your technique allow you to discriminatenondisjunction occurring during the first meioticdivision from nondisjunction occurring during thesecond meiotic division?The Drosophila chromosome 4 is extremely small;virtually no recombination occurs between genes onthis chromosome. You have available three differentlymarked chromosome 4s: one has a recessive allele ofthe gene eyeless (ey), causing very small eyes; one hasa recessive allele of the cubitus interruptus (ci) gene,which causes disruptions in the veins on the wings;and the third carries recessive alleles of both genes.Drosophila adults can survive with two or three, butnot with one or four, copies of chromosome 4.a. How could you use these three chromosomes tofind Drosophila mutants with defective meiosescausing an elevated rate of nondisjunction?b. Would your technique allow you to discriminatenondisjunction occurring during the first meioticdivision from nondisjunction occurring during thesecond meiotic division?c. What progeny types would you expect if a flyrecognizably formed from a gamete produced bynondisjunction were testcrossed to a fly homozygous for a chromosome 4 carrying both ey…