Unit 1 review Flashcards
(51 cards)
Draw out nitrogenous bases
Picture
Which nitrogenous bases are pyrimidines and purines
Pyrimidines: Cytosine, Thymine, Uracil
Purine: Guanine, Adenine
What is the name of the bond that holds nucleotides together in DNA and RNA.
Phosophodiester bonds between C and N terminus.
Hydrogen bonds between nitrogenous bases
What is the secondary structure of ds DNA?
Double Helix
What is the secondary structure of ssRNA and ssDNA?
Hair pin
What is DNA methylation. Why is it important?
DNA methylation is the addition of a methyl groups (CH3) to different nucleotides. It is important because it acts as an epigenetic mechanism to regulate gene expression by chemically modifying DNA without altering the underlying DNA sequence.
What would negative or positive supercoiling do in a bacterial chromosome?
Negative supercoiling: molecules are underwound: promotes process of DNA replication- makes DNA more accessible
Positive supercoiling: molecules are overrotated, hinders process of DNA replication- makes DNA less accessible
What is the difference between eukaryotic heterochromatin and euchromatin?
Heterochromatin: tightly packed, condensed form of chromatin with low transcriptional activity
Euchromatin: loosely packed form of chromatin with high transcriptional acitivity
Why does DNA wrap so well around nucleosomes?
Due to large positive charge
What is epigenetics?
Epigenetics are stable alterations to the chromatin structure that can be passed on to future generations, that do not alter the DNA sequence
What are telomeres? How are they replicated?
Telomeres: ends of chromosomes- rich in G repeats
Replication: During DNA replication, the lagging strands os synthesized in short okazaki fragments, requing RNA primers. When the final primer at the end is removed DNA polymerase can’t fill the gap due to there not being a pre-existing 3”-OH group. This leads to the progessive shortening of chromosome ends.
What is the evolutionary origin of chloroplasts and mitochondria? How can sequence comparisons support the evolutionary origin theory?
Evolutionary Origin of Chloroplasts: eukaryote engulfed cyanobacteria and formed an endosymbiotic relationship.
Evolutionary Origin of Mitochondria: eukaryote. engulfed proto-bacterium and formed an endosymbiotic relationship
Evidence:
- mitochondria and chloroplasts DNA resembles bacterial genome sequences (circular DNA)
- chloroplasts have double membrane ( supports engulfment event)
- replicate independently (binary fission)
What are the main 7 enzymes and proteins involved in DNA replication and what do they do. Draw on replication fork
- Helicase: unwinds double stranded DNA by breakung hydrogen bonds between pairs
- SS-Binding Proteins: Bind to single stranded DNA to prevent them from rewinding
- Topoisomerase (Gyrase in Prokaryotes): relives supercoiling ahead of replication fork
- Primase: synthesize short RNA primers to provide starting point for replication
- DNA Polymerase III: main enzyme- adds nuclotides to 3’ end of DNA
- DNA Polymerase I: Removes RNA primers and replaces them with DNA
- Ligase: links okazaki fragments
Differentiate between the leading and lagging strands in a replication fork.
Leading: 5’-3’ no breaks (top strand)
Lagging: 5’-3’ with breaks (okazaki fragments) (bottom strand)
What is an Okazaki fragment? What differentiates it from all other nucleotide strands?
Okazaki fragments: short segments of newly synthesized DNA on the lagging strand. Made in short bursts due to the anti-parallel nature of DNA
Differentiates:
- short length
- each okazaki fragments begin with RNA primers
- require DNA ligase for joining
Explain the problem of replicating the ends of linear chromosomes. How do eukaryotes and prokaryotes solve the problem?
Problem: progressive shortening of chromosomes
Solution: Telomerase: recognizes tip of repeate sequences- telomerase elongates the strand in the 5’-3’ direction and adds additional repeats. The overhang then has a primer added on the DNA polymerase can fill in the complementary strand
Recognize and describe the differences between
- DNA and RNA,
- DNA replication and RNA transcription,
- and DNA polymerases and RNA polymerase.
DNA
-deoxyribose (No -OH on C2 carbon)
- Bases: T:A G:C
- double stranded
- only one type of DNA
- only used to store genetic material
- only in nucleus
- DNA lasts long
- Self replicating
RNA
- Ribose (OH on C2 carbon)
- Bases: T:A G:U
- single stranded
- lots of types of RNA
- used for protein synthesis, gene regulation, and catalyze reactions
- RNA degrades easily
synthesized when needed
DNA Replication
- creates a copy of DNA for cell division
- uses DNA polyermase
- template is both strands of DNA
- produces two identical DNA strands
RNA Transcription
- creates RNA for protein synthesis or regulation
- uses RNA polymerase
- template is only on strand of DNA
- produces tRNA, mRNA, and rRNA
DNA Polymerase
- Function: synthesize new DNA during replication
- template: DNA
- Primer: needs RNA
RNA Polymerase
- Function: synthesizes new RNA during transciption
- template: DNA template
- Primer: doesn’t need primer
Draw a typical gene in prokaryotes with its regulatory elements.
Drawing
What is a 5’ or 3’ untranslated region in a prokaryotic gene?
its the noncoding region
Given a gene determine which strand is the coding strand and which is the template strand.
Coding strand (sense strand): This DNA strand has the same sequence as the mRNA, except it has T instead of U. It is not used directly in transcription.
Template strand (antisense strand): This is the strand that RNA polymerase reads to synthesize mRNA. It is complementary to the mRNA.
Provide an RNA sequence from a DNA template strand.
5’ GACT 3’
3’ CUGA 5’
Be able to translate an RNA open reading frame with a genetic code. (Give strategy)
Non Coding region- Start Codon AUG- Translated Region- Stop codon- None Coding region
Differentiate between rho independent and rho dependent transcriptional termination in prokaryotes.
Rho Independent terminators: are able to cause the termination only in the presence of an rho factor
Rho Dependent terminatorsL are able to cause the end of transcription in the absence of a rho factor
How is transcription and RNA modification different in eukaryotes and prokaryotes.
Eukaryotes
- Location: Transcription (Nucleus), Translation (Cytoplasm) Happens separately
- Polymerase: Pol 1, 2, 3
- Modifications: 5’ cap and polyadenylation
- Termination: Polyadenylation signal, and specific termination factors.
Prokaryotes
- Location: Both Transcription and Translation (Cytoplasm) Happens simultaneously
- Polymerase: Pol 1
- Modifications: none
- Terminators: Rho-independent, and dependent specific termination factors