Nucleic Acids - DNA Structure and Replication Flashcards
What (3) are nucleotides made up of?
1) Nitrogenous base
2) Phosphate group
3) Pentose sugar (Deoxyribose sugar)
Which nitrogenous bases are purines?
Adenine and guanine
What nitrogenous bases are pyrimidines?
Thymine and cytosine
What is the difference between purines and pyrimidines?
Purines have 2 rings whereas pyrimidines have 1 ring
How can the structure of DNA be described?
- double stranded
- antiparallel strands
- double helix
- has a major and minor groove
- sugar-phosphate backbone
What chemical bonds hold DNA together?
- Covalent phosphodiester bonds between 5’ of one sugar and 3’ of another
- Hydrogen bonds between base pairs
How many hydrogen bonds between adenine and thymine?
2 hydrogen bonds
How many hydrogen bonds between guanine and cytosine?
3 hydrogen bonds
What are the differences between DNA and RNA?
- the sugar in DNA is deoxyribose and in RNA it is ribose
- Bases in DNA are thymine, in RNA it is replaced by uracil
- Double stranded DNA and single stranded RNA
- DNA stores genetic material whereas RNA has many purposes
What are the 3 types of RNA?
- Coding
- Structural
- Regulatory
What is the role of coding RNA ?
- Messenger mRNA is translated into proteins, some mRNA is polycistronic
- RNA is also how some viruses store their genetic material e.g. HIV
What is the role of structural RNA?
- Ribosomal rRNA = make up ribosomes
- Transfer tRNA =carries amino acids to the ribosome in translation
what is the role of regulatory RNA
- microRNA = involved in post-transcriptional regulation of gene expression
- Xist (X inactivation specific transcript) = switches off one copy of the X chromosome in XX cells creating a Barr body
How is DNA packaged?
- DNA (-ve charge) bound to histone proteins (+ve) to form nucleosomes (10nm thick)
- Nucleosomes coiled to form chromatin fibres (30nm thick)
- chromatin fibres assembled on a protein scaffold to form a chromosome
How does semi-conservative replication occur?
1) DNA helicase breaks hydrogen bonds to unzip the helix, single stranded DNA binding proteins keep it unzipped, topoisomerase stops ‘overcoiling’
2) The enzyme primase attaches an RNA primer which acts as a start point to attach nucleotides.
3) DNA polymerase III adds nucleotides in a 5’ to 3’ direction starting from the primer.
4) Pol III has proofreading activity. If any wrong bases are incorporated, DNA polymerase can immediately remove the wrong base using 3-5 exonuclease activity.
5) On the lagging strand, new primers must reattach every time helicase unzips the next bit of DNA, new DNA polymerase adds bases until the next primer, results in lots of separate DNA fragments called okazaki fragments
6) RNA primers are removed and replaced with DNA by DNA polymerase I, Pol I has 5-3 polymerase and exonuclease activity
7) DNA ligase stitches the okazaki fragments together.