Problem 5.7 Part A How do mammals, including humans, solve the \"dosage problem\" caused by the presence of an X and Y chromosome in one sex and two X chromosomes in the other sex? Male RNA transcripts from the X chromosome have leaders that cause them to be translated at twice the rate as those in females. O Females produce twice the RNA transcripts as males do, but in females half of them are destroyed before being translated. O n males, the X chromosome is up-regulated so that its genes are transcribed and translated twice as much as the X chromosomes in females O They don\'t, but the X chromosome contains genes whose expression is not quantitatively sensitive, so the differences are not important. O They don\'t; the fact that females have twice as much X chromosome protein products as males is critical for sex determination in mammals. o n females, one of the X chromosomes is condensed and largely inactive so that each sex has one active X chromosome Submit My Answers Give Up Provide Feedback Continue Solution 1. Dosage compensation is the process by which the expression levels of sex-linked genes are altered in one sex to offset a difference in sex chromosome number between females and males of a heterogametic species. In case of humans, females have two copies of X chromosome(XX) and males have one(XY). Therefore, the females can produce twice as much gene product than the males,but it is due to Dosage Compensation that one of the X chromosomeis condensed and inactivated and hence the activity of X-linked genes is made equal in both the sexes. In case of placental mammals, i.e, marsupials Dosage Compensation is initiated by inactivation of one X chromosome in somatic cells of the females. 2. Down syndrome, one of the most familiar type of human trisomy in which affected individuals have an extra copy of chromosome 21 which is caused by nondisjunction of chromosome 21 during oogenesis. This incidence is related to maternal age, wherein with growing age of mothers there is a possibility that the chromosome tetrad during prophase I of meiosis will not remain together. Before birth, all oocytes are arrested in Diplotene stage in females. Once the beginning of menstrual period, meiosis resumes which indicates that the chromosomes in the tetrad must remain properly associated till menopause. Now, with maternal age there is a probability of these associations to break down which may lead to nondisjunction at Anaphase I..

1. Problem 5.7 Part A How do mammals, including humans, solve the "dosage problem" caused
by the presence of an X and Y chromosome in one sex and two X chromosomes in the other sex?
Male RNA transcripts from the X chromosome have leaders that cause them to be translated at
twice the rate as those in females. O Females produce twice the RNA transcripts as males do, but
in females half of them are destroyed before being translated. O n males, the X chromosome is
up-regulated so that its genes are transcribed and translated twice as much as the X chromosomes
in females O They don't, but the X chromosome contains genes whose expression is not
quantitatively sensitive, so the differences are not important. O They don't; the fact that females
have twice as much X chromosome protein products as males is critical for sex determination in
mammals. o n females, one of the X chromosomes is condensed and largely inactive so that each
sex has one active X chromosome Submit My Answers Give Up Provide Feedback Continue
Solution
1. Dosage compensation is the process by which the expression levels of sex-linked genes are
altered in one sex to offset a difference in sex chromosome number between females and males
of a heterogametic species. In case of humans, females have two copies of X chromosome(XX)
and males have one(XY). Therefore, the females can produce twice as much gene product than
the males,but it is due to Dosage Compensation that one of the X chromosomeis condensed and
inactivated and hence the activity of X-linked genes is made equal in both the sexes.
In case of placental mammals, i.e, marsupials Dosage Compensation is initiated by inactivation
of one X chromosome in somatic cells of the females.
2. Down syndrome, one of the most familiar type of human trisomy in which affected individuals
have an extra copy of chromosome 21 which is caused by nondisjunction of chromosome 21
during oogenesis. This incidence is related to maternal age, wherein with growing age of mothers
there is a possibility that the chromosome tetrad during prophase I of meiosis will not remain
together. Before birth, all oocytes are arrested in Diplotene stage in females. Once the beginning
of menstrual period, meiosis resumes which indicates that the chromosomes in the tetrad must
remain properly associated till menopause. Now, with maternal age there is a probability of these
associations to break down which may lead to nondisjunction at Anaphase I.