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For centuries, people have searched for the fabled Fountain of Youth, said to confer the ability to


forestall old age and remain young forever. To gain insight into how tackling aging by targeting


telomerase might work, researchers looked at mice that lack a telomerase gene. These mice have


shorter telomeres than normal mice and age prematurely. However, when these mice were engineered


to express telomerase in their somatic cells, their telomeres lengthen and the effects of aging are


reversed. This observation suggests that a drug that stimulates the expression of telomerase in somatic


cells could prevent telomere shortening and stop the aging process. Consider how such a drug would


work and what may be some potential side effects of such a drug?

A conditional mutation expresses its mutant phenotype only under the restrictive conditions and expresses the normal phenotype under the permissive conditions. One type of conditional mutation is a temperature-sensitive mutation, which expresses the mutant phenotype only at certain temperatures. Strains of E. coli have been isolated that contain temperature-sensitive mutations in the genes encoding different components of the replication machinery. In each of these strains, the protein produced by the mutated gene is non-functional under the restrictive conditions. These strains are grown under permissive conditions and then abruptly switched to the restrictive condition. After one round of replication under the restrictive condition, the DNA from each strain is isolated and analysed. What characteristics would you expect to see in the DNA isolated from each strain with a temperature-sensitive mutation in its gene that encodes a) DNA polymerase III, b) primase and c) initiator protein?

The regulation of replication is essential to genomic stability, and, normally, the DNA is replicated just


once every eukaryotic cell cycle (in the S phase). Normal cells produce protein A, which increases in


concentration in the S phase. In cells that have a mutated copy of the gene for protein A, the protein is


not functional and replication takes place continuously throughout the cell cycle, with the result that


cells may have 50 times the normal amount of DNA. Protein B is normally present in G1 but disappears


from the cell nucleus in the S phase. In cells with a mutated copy of the gene for protein A, the levels of


protein B fail to disappear in the S phase and, instead, remain high throughout the cell cycle. When the


gene for protein B is mutated, no replication takes place.


Propose a mechanism for how protein A and protein B might normally regulate replication so that each


cell gets the proper amount of DNA. Explain how mutation of these genes produces the effects just


described.

What cardiovascular factors affect blood pressure? ( short answer)


Why is it easier to measure the effects of smoking on individual’s health than it is to



measure the effects of anti-smoking campaigns on health?

correct me if I am wrong:


when K is less than 1, the concentration of reactants is greater than products. Delta G is negative, or exergonic and K>Q, has a forward reaction


when K is greater than 1, the concentration of products is greater than reactants. Delta G is positive, or endergonic, and K<Q, has a reverse reaction.


I might have them wrong in some way, but this is why I am confused.


Also, is this correct for delta Gº:


if delta Gº is positive, there is a greater amount of reactants, a reverse reaction is favored to reach equilibrium. And if delta Gº is negative, there is a greater amount of products, and a forward reaction is favored to reach equilibrium.


Scorpions are found in many areas of the world, except Antarctica. The table

below contains some information about scorpions


1. A woman's sister has cystic fibrosis, a disease caused by recessive genes. Neither of her parents has the disease. What chance is there that her mother is a carrier (heterozygous) for the trait? What chance is there that the woman herself is a carrier for the trait?  

2. Huntington's disease is a degenerative disease of the nervous system which does not show up until age 40. It is caused by a dominant gene. John's father just began to show the symptoms. What is the chance that John will have the disease?
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