Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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- Species I has 2 n = 16 chromosomes. How many chromosomes will be found per cell in the following mutants in this species? Q. Autotetraploidarrow_forwardPlease find the attachmentarrow_forward7.18 In Drosophila, the genes st (scarlet eyes), ss (spineless bris- tles), and e (ebony body) are located on chromosome 3, with map positions as indicated: SS e 58 70 st 44 Each of these mutations is recessive to its wild-type allele (st+, dark red eyes; sst, smooth bristles; et, gray body). Phenotypically wild-type females with the genotype st ss et/st stt sste were crossed with triply recessive males. Predict the phenotypes of the progeny and the frequen- cies with which they will occur assuming (a) no interfer- ence and (b) complete interference.arrow_forward
- Here are schematic diagrams of mutant Drosophila larvae. The left side of each pair shows a wild-type larva, with gray boxes showing the sections that are missing in the mutant larva. Which type of gene is defective in each larva: a gap gene, a pair-rule gene, or a segment-polarity gene?arrow_forwardIn a wild-type fungus, protein E (encoded by the haplosufficient gene E) normally dimerizes to catalyzes a biochemical reaction necessary for the production of a dark pigment. Ed represents a mutant, dominant negative allele of gene E. What is the predicted phenotype of a fungus cell of genotype E*/Ed, and why? O wild type (normal production of the dark pigment), as E is haplosufficient mutant (no pigment production), as no dimers will form in the heterozygous mutant (no pigment production), as the mutant allele Eg is dominant O wild type (normal production of the dark pigment), as dimers of wild-type and mutant protein E will be formed in the heterozygousarrow_forwardA pair of paralogous repeats, A and B, have 96% sequence similarity and therefore can promote non-allelic homologous recombination (NAHR). They exist in four possible arrangements in a genome, illustrated below as arrangements 1 – 4. What is the result of NAHR between repeats A and B in arrangement 1? A.Translocation between chromosomes 1 and 2 resulting in monocentric chromosomes B.Deletion or duplication of the region between A and B C.Translocation between chromosomes 1 and 2 resulting in acentric and dicentric chromosomes D.Inversion of the region between A and Barrow_forward
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