Nucleic Acid Structure Flashcards
What are the three core components of a nucleotide?
A phosphate backbone, a pentose sugar, and nitrogenous bases.
How does the number of phosphate groups vary in nucleotides?
The number of phosphate groups can range from 1 to 3 phosphates.
How does the 2’ carbon of a pentose sugar differentiate between RNA and DNA?
In RNA, the 2’ carbon is attached to a hydroxyl group (-OH), while in DNA, it is attached to a hydrogen (-H).
What is the significance of the base attached to the 1’ carbon in a nucleotide?
The chemistry of the nucleotide is largely dependent on the base attached to the 1’ carbon, which is critical from a molecular information perspective.
How are pyrimidines and purines different structurally?
Pyrimidines have one ring, while purines have two rings.
Which bases are purines and which are pyrimidines?
Purines are Adenine (A) and Guanine (G), while pyrimidines are Cytosine (C), Thymine (T), and Uracil (U).
Why is uracil not found in DNA?
Uracil is not found in DNA because of the spontaneous deamination of cytosine, which would convert it to uracil.
What are the chemical properties of nitrogenous bases?
Nitrogenous bases are weakly basic, aromatic molecules. Pyrimidines are planar, while purines have a slight pucker due to their two-ring structure.
What is the role of the sugar’s pucker in nucleotides?
The pucker of the sugar impacts the orientation of the phosphate group and the base, which influences DNA and RNA structures.
What is the difference between 2’-exo and 3’-exo conformations in nucleotide sugars?
2’-exo conformation is favored by deoxyribose (DNA), and 3’-exo conformation is favored by ribose (RNA).
What type of bond forms between the nitrogenous base and the pentose sugar?
A 1’ N-glycosidic bond forms between the nitrogenous base and the pentose sugar.
How does the N-glycosidic bond influence nucleotide conformation?
Bases usually adopt an anti conformation around the N-glycosidic bond in DNA. Pyrimidines cannot rotate into syn conformation due to steric hindrance, but purines can.
How are phosphate groups typically linked in nucleotides?
Phosphate groups are most commonly linked at the 5’ carbon on the pentose sugar, which is central in the formation of nucleotide polymers.
What roles do cyclic nucleotide structures like cAMP and cGMP play?
Cyclic nucleotides like cAMP and cGMP play important roles in cell signaling.
What type of bond links nucleotides in a nucleic acid polymer, and what is its directionality?
Phosphodiester bonds link nucleotides in a 5’ to 3’ direction, forming the sugar-phosphate backbone.
What is the structural difference between the 5’ and 3’ ends of a nucleotide chain?
The 5’ end has a free phosphate group, while the 3’ end has a free hydroxyl group.
In DNA, what causes the negatively charged backbone?
The negatively charged backbone is due to the free 3’ OH group at the end of the nucleotide chain and the phosphate groups along the backbone.
According to the Watson-Crick model, where are the sugar-phosphate backbone and nitrogenous bases located in the DNA structure?
The polar sugar-phosphate backbone is on the outside, and the nitrogenous bases are on the inside of the DNA helix.
What is the significance of the major groove in the DNA helix?
The major groove provides space for proteins, like transcription factors, to interact with the nitrogenous bases of the DNA.
How do the strands of DNA align with each other in the double helix?
The strands of DNA are antiparallel, meaning the 5’ end of one strand aligns with the 3’ end of the complementary strand.
What are the base-pairing rules according to Chargaff’s rules?
Adenine (A) pairs with Thymine (T) in DNA or Uracil (U) in RNA, and Guanine (G) pairs with Cytosine (C). Purines equal pyrimidines.