Genetics

Running head: GENETICS 1
Genetics
Name of Student
Institutional Affiliation
GENETICS 2
1. The process of DNA replication is linear and specific. Two distinct chemical
processes are involved, i.e. replication and transition. In replication,
deoxyribonucleotides are assembled linearly by a particular pairing of bases, forming
a replica of the original cellular structure. “This is followed by transcription, where
the genetic components produce messengers that transport protein-producing stations,
which is the information useful in defining the structure of the polypeptide chain”
(Rabeau, 2006). In this case, ribonucleotides are employed; while only one of the
DNA strands is employed in imitating into an RNA transcript. Replication of the cells
using N-15 achieves new replica, having the N-15 structure. Further, transition
process, where N-14 is used, only one of the original DNA strands are used, hence
resulting cells have N-15 and N-14 in the ratio 1:1.
2. a); b)
Percentage of bases based
on molarity
a)
b)
Organism
Adenine
Thymine
Guanine
Cytosine
(A+G)/(T+C)
(A+T)/(C+G)
Escherichia coli
26
23.9
24.9
25.2
1.04
1.00
Streptococcus pneumoniae
29.8
31.6
20.5
18
1.01
1.59
Yeast
31.7
32.6
18.3
17.4
1.00
1.80
Turtle red blood cells
28.7
27.9
22
21.3
1.03
1.31
Salmon sperm
29.7
29.1
20.8
20.4
1.02
1.43
Chicken red blood cells
28
28.4
22
21.6
1.00
1.29
Human liver cells
30.3
30.3
19.5
19.9
0.99
1.54
c) Some of the ratios happen to be constant in a but vary in b; “because the mobility
of the different molecules varies depending on certain conditions” (Randerath,
1964), hence a direct effect on the rate of replication.
GENETICS 3
3. There are more H2A histone molecules than H1 histone molecules in a chromatin
because “the H2A molecules have an active role in transcriptional silencing” (Filion,
2010). This means that they act as regulators to the process of cell multiplication
through transcription. I would not expect to find more H2A or more H3 histone
molecules in a chromatin; because these are involved in many detrimental processes,
e.g. ribosome formation, DNA repair, transcription activity among others. Thus, the
need for a regulated process for a functional cellular system.
4. DNA replication in a eukaryotic cell. “DNA replication process” (Jacob, 1963).
GENETICS 5
5. Definitions:
a. DNA helicase: this is the enzyme that is responsible for facilitation of DNA
replication, through unzipping of DNA strands to allow attachment and expose the
nucleotides used as templates in the process.
b. DNA polymerase I: a specially designed enzyme that helps in the process of DNA
replication, through removing the RNA primer and filling the nucleotides which
are necessary for the formation of DNA in the 5' to 3' direction. Furthermore, it
proof-reads, to ensure there are no mistakes in the replication while matching the
base pairs.
c. DNA polymerase III: this is an enzyme responsible for facilitating DNA
replication, mainly through accelerating the replication of the leading and lagging
strands.
d. DNA ligase: this is the enzyme responsible for joining nucleotides during DNA
replication, thus forming continuous DNA strands.
e. Primase: this is an enzyme that synthesizes RNA primers during DNA replication.
f. Topoisomerase: this refers to drugs that have an effect on the DNA replication
process, and are thus used in order to alter a DNA replication process. For
instance, during cell division, chromosomes separate from one another after
exchanging information through recombination. Thus, a chromosome can be
exchanged for DNA in a sister chromosome molecule, in order to alter genetic
information. This is made possible through topoisomerases.
g. Telomerase: these refer to the end regions of the DNA chromosomes, which
consist of telomeric repeat sequences. These ensure that there is the replication of
a complete version of each chromosome to avoid DNA damage or losses.
GENETICS 6
h. Single-strand binding proteins: this refers to a type of protein mainly found in
Escherichia Coli bacteria, that binds itself to regions of DNA that have only one
strand.
GENETICS 7
References
Filion, G. J., van Bemmel, J. G., Braunschweig, U., Talhout, W., Kind, J., Ward, L. D., ... &
van Steensel, B. (2010). Systematic protein location mapping reveals five principal
chromatin types in Drosophila cells. Cell, 143(2), 212-224.
Jacob, F., Brenner, S., & Cuzin, F. (1963, January). On the regulation of DNA replication in
bacteria. In Cold Spring Harbor Symposia on Quantitative Biology (Vol. 28, pp. 329-
348). Cold Spring Harbor Laboratory Press.
Rabeau, J. R., Reichart, P., Tamanyan, G., Jamieson, D. N., Prawer, S., Jelezko, F., ... &
Wrachtrup, J. (2006). Implantation of labeled single nitrogen-vacancy centers in
diamond using N 15. Applied Physics Letters, 88(2), 023113.
Randerath, K., & Randerath, E. (1964). Ion-exchange chromatography of nucleotides on
poly-(ethyleneimine)-cellulose thin layers. Journal of Chromatography A, 16, 111-
125.

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