c. i. Identify a field of research, other than dyskeratosis congenita, that could use knowledge gained about telomerase and telomeres. Explain how this information might be used. c. ii. Evaluate how this research could affect either an individual or society. Include one potential advantage and one potential disadvantage in your evaluatior

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Use the following additional information to
answer the next two parts of the question.
Knowledge that researchers have gained
about telomerase through their study of
dyskeratosis congenita could be of use to
researchers in other fields of study.
c. i. Identify a field of research, other than
dyskeratosis congenita, that could use
knowledge gained about telomerase and
telomeres. Explain how this information might
be used.
c. ii. Evaluate how this research could affect
either an individual or society. Include one
potential advantage and one potential
disadvantage in your evaluatior
Transcribed Image Text:Use the following additional information to answer the next two parts of the question. Knowledge that researchers have gained about telomerase through their study of dyskeratosis congenita could be of use to researchers in other fields of study. c. i. Identify a field of research, other than dyskeratosis congenita, that could use knowledge gained about telomerase and telomeres. Explain how this information might be used. c. ii. Evaluate how this research could affect either an individual or society. Include one potential advantage and one potential disadvantage in your evaluatior
From the time that a sperm cell first fertilizes
an egg cell, a "biological clock" begins ticking
within the zygote. The number of times that
cells, all of which come from the original
zygote, will be able to divide is limited.
On each end of a chromosome is a structure
known as a telomere. Each time the DNA
replicates, teh telmere shortens. This
progressive shortening will eventually cause
the telomere length to shorten to the point
that the DNA will no longer be able to
replicate, causing the cell to die. An enzyme
known as telomerase is found in rapidly
dividing cells, such as those in the testes, skin,
hair, and bone marrow. Telomerase lengthens
telomeres so that a cell can continue to divide.
Dyskeratosis congenita is an inherited human
disorder in which patients have reduced
telomerase activity. Affected individuals die
between the ages of 16 and 50 years. Death is
usually associated with bone marrow failure,
although the patient will exhibit many other
symptoms. Kyskeratosis congenita is caused by-
la mutation in either the X chromosome or an
autosome. In the sex-linked disorder, affected
individuals have low levels of telomerase and
they have shoerter-than-normal telomeres in
various cells. In the autosomal disorder,
affected individuals can be heterozygous. In
some autosomal patients, a segment of 821
base pairs of the telomerase gene has been
deleted. In other patients, one or two nitrogen
base pair substitutions have occurred.
Transcribed Image Text:From the time that a sperm cell first fertilizes an egg cell, a "biological clock" begins ticking within the zygote. The number of times that cells, all of which come from the original zygote, will be able to divide is limited. On each end of a chromosome is a structure known as a telomere. Each time the DNA replicates, teh telmere shortens. This progressive shortening will eventually cause the telomere length to shorten to the point that the DNA will no longer be able to replicate, causing the cell to die. An enzyme known as telomerase is found in rapidly dividing cells, such as those in the testes, skin, hair, and bone marrow. Telomerase lengthens telomeres so that a cell can continue to divide. Dyskeratosis congenita is an inherited human disorder in which patients have reduced telomerase activity. Affected individuals die between the ages of 16 and 50 years. Death is usually associated with bone marrow failure, although the patient will exhibit many other symptoms. Kyskeratosis congenita is caused by- la mutation in either the X chromosome or an autosome. In the sex-linked disorder, affected individuals have low levels of telomerase and they have shoerter-than-normal telomeres in various cells. In the autosomal disorder, affected individuals can be heterozygous. In some autosomal patients, a segment of 821 base pairs of the telomerase gene has been deleted. In other patients, one or two nitrogen base pair substitutions have occurred.
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