Biology: The Unity and Diversity of Life (MindTap Course List)
Biology: The Unity and Diversity of Life (MindTap Course List)
14th Edition
ISBN: 9781305073951
Author: Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr
Publisher: Cengage Learning
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Chapter 13, Problem 4GP
Summary Introduction

To explain: The probability that one of the surviving kittens with parents having the allele MLM associated with taillessness in Manx cats will be heterozygous.

Concept introduction: The mutated ML allele is associated with taillessness in Manx cats. The homozygous MLML allele is called as lethal alleles, as they cause death of the kitten as embryo itself due to defects of the spinal cord. Lethal alleles are those in heterozygous or homozygous form that causes death of the individual during embryonic development itself. The probability reduces in such cases, as those alleles will not be transferred to the next generation as the allele is lost with the death of the embryo.

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In cats, the locus for orange coat color is sex linked. Male cats that are black have the o+ allele, whereas those that are orange have the o allele. Females can be homozygous for the orange allele or homozygous for the black allele and will express each color, respectively. Heterozygous females are tortoise-shelled or calico, having orange and black patches. A calico cat, in addition to being heterozygous at the orange locus, also is either heterozygous or homozygous for the incompletely dominant, autosomal spotting allele (SS = large spots, Ss = small spots, ss = no spots). Manx tails are caused by a dominant trait that is lethal when homozygous. Long tails are the result of a homozygous recessive genotype. An orange male with small white spots and a manx tail is crossed to a calico female with small white spots and a manx tail. What is the probability of observing a solid black female with no spots and long tail? (Hint: All calico cats are female!)
In fruit flies, the dominant H allele gives rise to a hairless phenotype, hh gives rise to normal body bristles, and the HH homozygote condition is lethal during an embryonic stage.  The presence of a dominant S allele suppresses the effect of the dominat H allele with respect to the body bristles phenotype such that normal body bristle phenotype is restored when only one dominant H allele is present (HH is lethal irrespective of the S or s alleles). The ss genotype has no effect over the H allele and the SS homozygote condition is also lethal during an embryonic stage.  What would be the expected phenotypic outcomes among the surviving offspring from the following cross: HhSs   X   hhSs   2 normal body bristles: 1 hairless 7 normal body bristles: 2 hairless 1 normal body bristles: 1 hairless 3 normal body bristles: 1 hairless 5 normal body bristles: 1 hairless
The ABO blood groups in humans are expressed as the IA, IB, and i alleles. The IA allele encodes the A blood group antigen, IB encodes B, and i encodes O. Both A and B are dominant to O. If a heterozygous blood type A parent (IAi) and a heterozygous blood type B parent (IBi) mate, one quarter of their offspring will have AB blood type (IAIB) in which both antigens are expressed equally. Therefore, ABO blood groups are an example of: a. multiple alleles and incomplete dominance b. codominance and incomplete dominance c. incomplete dominance only d. multiple alleles and codominance
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