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This document offers a comprehensive overview of nucleic acids, focusing on the structure and function of dna and rna. it details the components of nucleotides, including sugars (ribose and deoxyribose), nitrogenous bases (purines and pyrimidines), and phosphate groups. base pairing rules, the double helix structure of dna, and the processes of replication, transcription, and translation. it also includes mnemonic devices to aid in memorization and clarifies key differences between dna and rna.
Typology: Lecture notes
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DNA stores genetic information. RNA converts genetic information into proteins.
Just like amino acids are the building blocks of proteins, nucleotides are the building blocks of both RNA and DNA.
Every nucleotide consists of three components:
A phosphate group A five-carbon sugar A nitrogenous base (amine)
The five-carbon sugar, also called a carbohydrate, is where the fundamental difference between DNA and RNA lies.
One type of nucleotide contains ribose. The other contains deoxyribose.
In nucleotides, the sugar carbons are numbered with primed numbers (1', 2', 3', 4', 5') to differentiate them from the nitrogenous base numbering.
The key difference between ribose and deoxyribose is at the 2' carbon position.
Ribose has an oxygen (OH) at the 2' position. Deoxyribose has only a hydrogen (H) at the 2' position. The "D" in DNA stands for "deoxy," indicating the removal of an oxygen.
The 3' carbon position is identical in both sugars and always has an OH group.
The numbering of the sugars is essential when discussing how nucleotides align in an anti-parallel manner to form a helix, known as the 5' end and 3' end.
Identifying DNA vs RNA
To determine if a molecule is RNA or DNA, look at the 2' carbon:
If there is an oxygen, it's RNA (ribose). If there is only a hydrogen, it's DNA (deoxyribose).
Other Terms for the Sugar Component
Pinto Sugar Carbohydrate Sugar
Nitrogenous Bases
The nitrogenous bases are amine bases. There are two categories of nitrogenous bases:
Pyrimidines Purines
To determine if a sugar is deoxyribose or ribose, look at the 2' position. If there is nothing on the 2' position, it is deoxyribose.
Linking Nucleotides and Phosphodiester Bonds
Nucleotides link together through phosphodiester bonds. Instead of a carbon, there is a phosphorus in the bond. The bond occurs on the carbon.
Backbone Structure of DNA
The backbone of a DNA molecule consists of alternating sugar and phosphate groups. The amine bases are bonded off away from the backbone. The pattern, like the primary sequence for amino acids, also exists for nucleic acids.
Colorful Picture of Phosphodiester Bond
The 3' position of the sugar (ribose or deoxyribose) bonds to the phosphate group. This results in a 3' end at the bottom and a 5' end at the top of the molecule.
Carbon Numbering
The numbers with primes (e.g., 3', 5') come from the numbering of carbons in carbohydrates (C1, C2, C3, C4, C5). The prime numbers are used because the base atoms get the non-prime numbers.
Visual Representation of DNA Structure
Sugar, phosphate, sugar, phosphate pattern with amine bases sticking out. Recognition of the 5' end is important. It is a 5' end because the phosphate ends with the 5' carbon bond (C5').
The double helix shape in DNA is due to a single ring bonded to a double ring. Purines (double rings) take up more space than pyrimidines (single rings). To maintain the fit, a pyrimidine always bonds to a purine. In DNA: Adenine (A) always bonds to Thymine (T). Guanine (G) always bonds to Cytosine (C). Examples of mnemonic devices for remembering base pairing: Apples on a Tree (A and T) and Cars in the Garage (C and G) Appalachian Trail (AT) and Gas Chromatography (GC)
It is important to be able to connect base pairs because we will be looking at DNA- based pairs.
Come up with a way to remember how to connect base pairs.
GC: General Contractor, Gas Chromatography AT: Art Teacher
The order of the base pairs does not matter, only that they are always paired to each other.
Adenine (A) and Thymine (T) have two hydrogen bonds. Guanine (G) and Cytosine (C) have three hydrogen bonds.
Hydrogen bonding is anytime a hydrogen is bonded to either a nitrogen, an oxygen, or a fluorine.
Up until now, we've pretty much been talking about DNA, a nucleotide where we have deoxyribose.
Hydrogen bonds hold complementary base pairs together.
When in doubt in chemistry or biochemistry, guessing hydrogen or cholesterol, respectively, often leads to the correct answer.
Phosphodiester bonds hold nucleotides together in a strand.
The double helix structure of DNA is due to:
A pyrimidine always bonding to a purine, ensuring consistent sizing. The specific sizes of these bases and the hydrogen bonding between them result in efficient packing and the characteristic double helix shape.
DNA consists of two strands described as anti-parallel. This means they are parallel but oriented in opposite directions.
One strand runs 5' to 3', having a free 5' carbon at one end and a free 3' carbon at the other. The other strand runs 3' to 5', with the order inverted.
In a 5' to 3' strand, the backbone consists of sugar, phosphate, sugar, phosphate, and so on.
Given a DNA sequence, you can write its complementary base sequence:
Example:
If the primary sequence (5' to 3') is T C G A, then the complementary base sequence (3' to 5') is A G C T.
The backbone consists of repeating units of sugar and phosphate, with each sugar attached to a base.
You don't need to memorize the structures of the bases. You should be able to identify whether a base is a pyrimidine or a purine.
Given a sequence with the 5' end identified, and the bases labeled (e.g., G, T, A, C), you can write the complementary base pair sequence.
For example, if you have a sequence 5'-G T A C-3', the complementary sequence would be 3'-C A T G-5'.
It is conventional to write DNA sequences from 5' to 3'. Even if a sequence is presented "backwards" (starting with 3'), you can still determine the complementary sequence by starting with 5' and following the base pairing rules.
Information from DNA is copied into a new molecule of RNA, specifically messenger RNA (mRNA). Uracil (U) replaces thymine (T) in RNA.
mRNA is translated into proteins using codons. Codons are groups of three bases on the mRNA.
A codon is three nucleotide or base sequences in mRNA. Each codon corresponds to a specific amino acid.
The sequence of codons determines the sequence of amino acids, forming the primary structure of a protein.
Codon charts are used to determine which amino acid is encoded by a specific codon.
The codon CCA codes for proline.
The codon AUG codes for methionine.
Codons are used to translate RNA into proteins. A codon chart helps decipher the relationship between mRNA sequences and the corresponding amino acids. The primary sequence, or the order of codons, determines the specific protein. Exam will have a codon chart available, either as a header or footer.
Always read the chart in the 5' to 3' direction. Use the chart to translate mRNA into amino acids. Multiple codons can code for the same amino acid, meaning the code is degenerate.
A nucleoside is essentially a nucleotide without the phosphate group.
A nucleoside is a nucleotide without the phosphate group. It's a precursor to a nucleotide.