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What are the mechanisms by which these mutations alter normal cellular processes, leading to the uncontrolled cell growth seen in cancer or the neurodegeneration observed in Alzheimer’s disease?
Mandalien disorders : ●It is a genetics disorder ●Chromosomes does not changes ●Only single gene is involved ●Cause mutation in single gene ●Also called as monotonic disorder ●Either dominant or recessive EX: 1.Haemophilia 2.sickle cell anemia 3.phenylketonuria 4.color blindness 5.thalassemia 6.cystRead more
Mandalien disorders :
●It is a genetics disorder
●Chromosomes does not changes
●Only single gene is involved
●Cause mutation in single gene
●Also called as monotonic disorder
●Either dominant or recessive
EX:
1.Haemophilia
2.sickle cell anemia
3.phenylketonuria
4.color blindness
5.thalassemia
6.cystic fibrosis
Non-mendelian disorder :
●It is a genetic disorder
●Cause error in cell division following meiosis and mitosis
●Chromosomes changes
●More than one gene is involved
●called as chromosomal disorder Neither dominant or recessive
EX:
1.Allosomal disorder
a.Klinefelter’s syndrome
b.Turner’s syndrome
2.Autosomal disorder
a .Down syndrome
b.Edwards syndrome
c.Patau syndrome
d.Cri-du-chat syndrome
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DNA replication in eukaryotes occurs in three stages: initiation, elongation, and termination. Initiation Eukaryotic DNA is bound to proteins known as histones to form structures called nucleosomes. During initiation, the DNA is made accessible to the proteins and enzymes involved in the replicationRead more
DNA replication in eukaryotes occurs in three stages: initiation, elongation, and termination.
Eukaryotic DNA is bound to proteins known as histones to form structures called nucleosomes. During initiation, the DNA is made accessible to the proteins and enzymes involved in the replication process. There are specific chromosomal locations called origins of replication where replication begins. Certain proteins recognize and bind to the origin of replication and then allow the other proteins necessary for DNA replication to bind the same region.
Two copies of an enzyme called helicase are among the proteins recruited to the origin. Each helicase unwinds and separates the DNA helix into single-stranded DNA. As the DNA opens up, Y-shaped structures called replication forks are formed. Because two helicases bind, two replication forks are formed at the origin of replication; these are extended in both directions as replication proceeds creating a replication bubble. There are multiple origins of replication on the eukaryotic chromosome which allow replication to occur simultaneously in hundreds to thousands of locations along each chromosome.
During elongation, an enzyme called DNA polymerase adds DNA nucleotides to the 3′ end of the newly synthesized polynucleotide strand. The template strand specifies which of the four DNA nucleotides (A, T, C, or G) is added at each position along the new chain. Only the nucleotide complementary to the template nucleotide at that position is added to the new strand.
DNA polymerase cannot initiate new strand synthesis; it only adds new nucleotides at the 3′ end of an existing strand. All newly synthesized polynucleotide strands must be initiated by a specialized RNA polymerase called primase.
Primase initiates polynucleotide synthesis and by creating a short RNA polynucleotide strand complementary to template DNA strand. This short stretch of RNA nucleotides is called the primer. Once RNA primer has been synthesized at the template DNA, primase exits, and DNA polymerase extends the new strand with nucleotides complementary to the template DNA.
DNA polymerase can only synthesize new strands in the 5′ to 3′ direction. Therefore, the two newly-synthesized strands grow in opposite directions because the template strands at each replication fork are antiparallel. The “leading strand” is synthesized continuously toward the replication fork as helicase unwinds the template double-stranded DNA.
The “lagging strand” is synthesized in the direction away from the replication fork and away from the DNA helicase unwinds. This lagging strand is synthesized in pieces because the DNA polymerase can only synthesize in the 5′ to 3′ direction, and so it constantly encounters the previously-synthesized new strand. The pieces are called Okazaki fragments, and each fragment begins with its own RNA primer.
Once all the template nucleotides have been replicated, the replication process is not yet over. RNA primers need to be replaced with DNA, and nicks in the sugar-phosphate backbone need to be connected.
The group of cellular enzymes that remove RNA primers include the proteins FEN1 (flap endonulcease 1) and RNase H. The enzymes FEN1 and RNase H remove RNA primers at the start of each leading strand and at the start of each Okazaki fragment, leaving gaps of unreplicated template DNA. Once the primers are removed, a free-floating DNA polymerase lands at the 3′ end of the preceding DNA fragment and extends the DNA over the gap. However, this creates new nicks (unconnected sugar-phosphate backbone).
In the final stage of DNA replication, the enyzme ligase joins the sugar-phosphate backbones at each nick site. After ligase has connected all nicks, the new strand is one long continuous DNA strand, and the daughter DNA molecule is complete.
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Genetic Modification is the next buzz field in the life sciences industry. Gene editing technology has been developed that helps scientists now splice genes, and combine genes in lab setups to create modifications within any biological system. The presence of ...
The control of designer babies by means of the gene modification techniques is one of the most burning questions in bioethics. Advocates have said using the tool can remove hereditary diseases in human beings, thus, have healthier people and end up lowering healthcare costs. It also might pave the wRead more
The control of designer babies by means of the gene modification techniques is one of the most burning questions in bioethics. Advocates have said using the tool can remove hereditary diseases in human beings, thus, have healthier people and end up lowering healthcare costs. It also might pave the way for further developments of society since the given tech contributes to the increase in human IQ, physical performance, and immunity to certain diseases.
Nonetheless, there are severe ethical issues to ponder concerning this topic. There is concern that off-target effects and new health instances may also occur, which is a main concern. Further, there is also the danger of increasing social injustice where the few with money can afford to get gene editing while the rest cannot. Designer babies provoked the problem of converting people into commodities: making people according to one’s preferences rather than the genetic differences of the world. This might lead to the reduction of diversity and people are forced to fit certain categories or image.
Furthermore, nobody knows how the overall human genes will be affected in short, middle, or Long run, there are ethical questions as to how much people should tinker with the natural acts of evolution. Therefore, based on the evaluation of risks and benefits along with the consideration of the possible social consequences, gene modification for creating designer babies can be ethically acceptable if the regulation of access is done properly with proper ethical considerations.
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