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Essential Cell Biology 5th edition

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Answers A:17

H

N

N

adenine

N

N

H

NH 2

NH 2

N

O

circular DNA

linear DNA

H

N

hypoxanthine

N

N

H

HO

5′ 3′

REMOVAL OF RNA

PRIMER

template strand

new strand

RNA primer

OH 3′

5′

O

O

H

H 2 N

N

N

guanine

N

N

H

H

N

O

xanthine

N

H

N

N

H

5′

HO

3′

DNA SYNTHESIS

5′

OH 3′

H

H

cytosine

N

N

O

H

H

uracil

O

N

N

H

O

(A)

Figure A6−14

(B)

5′

LOST

NUCLEOTIDES

OH 3′

H 3 C

H

thymine

H

H

uracil

Figure A6−13

O

N

O

N

N

N

H

O

H

O

NO CHANGE

NO CHANGE

(as it is in RNA), repair enzymes could not distinguish

whether a uracil is the appropriate base or whether it arose

through spontaneous deamination of cytosine. This dilemma

is not encountered, however, because thymine, rather than

uracil, is used in DNA. Therefore, if a uracil base is found in

ECB5 EA6.13/A6.13

DNA, it can be automatically recognized as a damaged base

and then excised and replaced by cytosine.

ANSWER 6–14

A. DNA polymerase requires a 3ʹ-OH to synthesize DNA;

without telomeres and telomerase, the ends of linear

chromosomes would shrink during each round of DNA

replication. For bacterial chromosomes, which have no

ends, the problem does not arise; there will always be

a 3ʹ-OH group available to prime the DNA polymerase

that replaces the RNA primer with DNA (Figure A6−14).

Telomeres and telomerase prevent the shrinking of

chromosomes because they extend the 3ʹ end of the

template DNA strand (see Figure 6−23). This extension

of the lagging-strand template provides the “space” to

begin the final Okazaki fragments.

B. As shown in Figure A6−14A, telomeres and telomerase

are still needed even if the last fragment of the lagging

strand were initiated by primase at the very 3ʹ end of

chromosomal DNA, inasmuch as the RNA primer must

be removed.

ECB5 A6.14

ANSWER 6–15

A. If the single origin of replication were located exactly in

the center of the chromosome, it would take more than

8 days to replicate the DNA

[= 75 × 10 6 nucleotides/(100 nucleotides/sec)]. The rate

of replication would therefore severely limit the rate of

cell division. If the origin were located at one end, the

time required to replicate the chromosome would be

approximately double this.

B. A chromosome end that is not “capped” with a telomere

would lose nucleotides during each round of DNA

replication and would gradually shrink. Eventually,

essential genes would be lost, and the chromosome’s

ends might be recognized by the DNA damage-response

mechanisms, which would stop cell division or induce cell

death.

C. Without centromeres, which attach mitotic chromosomes

to the mitotic spindle, the two new chromosomes that

result from chromosome duplication would not be

partitioned accurately between the two daughter cells.

Therefore, many daughter cells would die, because they

would not receive a full set of chromosomes.

Chapter 7

ANSWER 7–1 Perhaps the best answer was given by

Francis Crick himself, who coined the term in the mid-1950s:

“I called this idea the central dogma for two reasons, I

suspect. I had already used the obvious word hypothesis

in the sequence hypothesis, which proposes that genetic

information is encoded in the sequence of the DNA

bases, and in addition I wanted to suggest that this new

assumption was more central and more powerful…. As it

turned out, the use of the word dogma caused more trouble

than it was worth. Many years later Jacques Monod pointed

out to me that I did not appear to understand the correct

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