The DNA changes that are described in Henry’s story are changes to the coding strands of the CYP2C9 genes. What is the function of the coding strand and how does it differ from the function of the template strand of Henry’s CYP2C9 gene? The function of a coding strand is the strand that is going to be transcribed. The function of a template strand is the complementary strand from the coding strand. The template strand is what is used as a template in the synthesis of
The first step of DNA replication is the unwinding of the two individual strands of DNA that are together in a structure that is known as a “double helix”, a term coined by Watson and Crick, who founded the first original model of DNA. The enzyme that is used to split the two strands is called helicase, and the splitting process starts in a place called the “origin of replication”. After each separate DNA strand has successfully unwound, the bases that are present on the strands are now exposed, and unpaired. The enzymes then match the bases with the free nucleotide triphosphates. The bases used in DNA replication are adenine (A), thymine (T), guanine (G), and cytosine (C).
This is the restriction enzyme and acts as “molecular scissors” cuts the two DNA chains at a specific area in the genome so that sections of DNA can be supplemented or detached. A piece of RNA known as guide RNA is the second key molecule. This consists of pre-designed RNA quite small in length sequence, consisting of about 20 bases, positioned within a longer RNA scaffold. The scaffold binds to DNA and the pre-designed sequence ‘guides’ Cas9 to the right part of the genome. ensuring that the Cas9 enzyme intersects at the right point in the genome.
Portions of the DNA molecule useful for DNA typing: a. Code for the production of proteins b. Are useful for recombinant DNA c. Are repeated many times d. Are useful for the production of insulin e. Can determine if a person has sickle-cell anemia 6. The concept of simultaneously extracting, amplifying, and detecting a combination of STRs is known as: a. PCR b. THO1 c. Multiplexing d. Electrophoresis e. Polymarker 7. Which statement is not correct for Y-STRs?
Synthesis, processing, and functionThe brief existence of an mRNA molecule begins with transcription and ultimately ends in degradation. During its life, an mRNA molecule may also be processed, edited, and transported prior to translation. Eukaryotic mRNA molecules often require extensive processing and transport, while prokaryotic molecules do not.  TranscriptionMain article: Transcription (genetics) Transcription is when DNA makes RNA. During transcription, RNA polymerase makes a copy of a gene from the DNA to mRNA as needed.
Enzymes called topoisomerases produce breaks in the DNA molecules and then reconnect the strands, relieving strain and effectively preventing tangling and knotting during replication. DNA polymerase adds new nucleotides to a growing strand of DNA. Because DNA polymerase must adhere to an existing template, an RNA primer is first created at the site of replication. The RNA primer is synthesized by primase, an enzyme that is able to start a new strand of RNA opposite a DNA strand. After a few nucleotides have been added, the primase is displaced by DNA polymerase, which can then add subunits to the 3’ end of the short RNA primer.
Proteins are formed through condensation reactions which bond amino acids together with peptide bonds in a particular sequence and the type of protein that is created is defined by the unique sequence of the amino acids. DNA and RNA are nucleic acids that are formed in the nucleotides and are both involved in the process of protein synthesis. Deoxyribonucleic acid, more commonly known as DNA, is located within the nucleus of the cell and contains the entire genetic code for an organism within its structure. DNA has two very important functions which are: to convey information from one generation of cells to the next by the process of DNA replication and to provide the information for the synthesis of proteins necessary for cellular function. Basically, DNA controls protein synthesis.
Transgenesis and Cloning Transgenesis is the process of inserting a gene from one source into a living organism that would not normally contain the inserted gene. The gene can come from the same species (called Cisgenesis) or from a different species entirely. To facilitate the transfer of genes from one organism to another, often a Transgenic Organism with Recombinant DNA is created: -The first step in creating an organism capable of carrying out the transformation process is to isolate the required gene. This is done so using Restriction Enzymes, which target a specific gene sequence. The gene is often cut with staggered ends, called “Sticky Ends” which only allow specific and complementary gene sequences bond by base pairing.
There has to be primers to start the synthesis at the 3’ end of the new strands. The RNA primers are later replaced with DNA. Leading & Lagging Strands DNA splits into 2 strands. The continuous strand (the leading strand), and the discontinuous strand (the lagging strand) that grows away from the replication fork. Death Cap Mushroom Transcription and Translation: mRNA is necessary to direct synthesis (transcription) of the polypeptides.
DNA methylation also occurs during the differentiation of adult cells. In both instances, methylation takes place almost exclusively on cytosine bases adjacent to a guanine, a combination called a CpG dinucleotide. Many of these dinucleotides are clustered in regions, called CpG islands, located in and near promoter sequences adjacent to genes. Islands adjacent to essential genes (housekeeping genes) and cell-specific Genes are unmethylated, making these genes available for transcription. Other genes with adjacent methylated CpG islands are transcriptionally silenced.