process in which one strain of bacteria is changed by a gene or genes from another strain of bacteria | transformation |
kind of virus that infects bacteria | bacteriophage |
principle that bonds in DNA can form only between adenine and thymine and between guanine and cytosine | base pairing |
monomer of DNA - consists of a sugar, phosphate group, and a nitrongenous base | nucleotide |
there are four of these in DNA - adenine, thymine, cytosine, and guanine; biologists will often refer to these by the first letters of the each | nitrogen base |
these are in between the sugars in the DNA backbone and are negatively charged | phosphate group |
this is the type of sugar in DNA and connects to the phosphate group and the nitrogen base | deoxyribose sugar |
this is the type of sugar in RNA and connects to the phosphate group and the nitrogen base | ribose sugar |
a self-replicating material that is present in nearly all living organisms as the main constituent of chromosomes. It is the carrier of genetic information | DNA |
this is the single stranded information molecule in all organisms; principal role is to act as a messenger carrying instructions from DNA for controlling the synthesis of proteins, although in some viruses this molecule, rather than DNA carries the genetic information | RNA |
process of copying DNA prior to cell division; uses several enzymes to speed up the process | DNA Replication |
repetitive DNA at the end of a eukaryotic chromosome | Telomer |
principle enzyme involved in DNA replication; adds nucleotides to a growing strand of DNA from the 5' to the 3' direction | DNA polymerase III |
an enzyme that joins DNA strands together by forming a bond between a 5' phosphate and a 3' hydroxyl group at the ends of the DNA fragments | DNA ligase |
an enzyme that separates the two strands of a DNA molecule, breaking the hydrogen bonds between base pairs | DNA helicase |
a short strand of single-stranded nucleic acid that acts as a starting point for DNA synthesis in living organisms | RNA primer |
proteins that play a vital role in DNA replication, recombination, and repair specifically, for the purpose of our course, they work with other enzymes to keep the single stranded DNA (ssDNA) from breaking down | Single stranded binding proteins (SSBP) |
one of two new DNA strands that are synthesized during DNA replication in the same direction as the replication fork | Leading strand |
this strand strand is synthesized in small fragments, called Okazaki fragments, in the opposite direction of the replication fork | Lagging strand |
short DNA pieces that form during the discontinuous replication of the lagging strand of DNA | Okazaki Fragments |
a single stranded nucleic acid molecule found in most living organisms and viruses; backbone is made of alternating phosphate groups and ribose sugar | RNA |
a single-stranded molecule of ribonucleic acid (RNA) that carries genetic information from DNA in the nucleus of a cell to the cytoplasm, where proteins are made | mRNA |
a small RNA molecule that plays a vital role in protein synthesis by acting as a link between messenger RNA (mRNA) and amino acids | tRNA |
a non-coding RNA molecule that's a key component of ribosomes, which are organelles that synthesize proteins in cells | rRNA |
process of copying a segment of DNA into RNA | transcription |
process in living cells in which proteins are produced using RNA molecules as templates | translation |
noncoding DNA sequence within a gene that is removed before the RNA molecule is translated into a protein | intron |
a section of a gene that is part of the mature RNA produced by that gene after RNA splicing removes introns | exon |
MB Questions
Activators bind to DNA enhancer regions.
Other choices: RNA polymerase, promoters, introns, exons
Activators are a type of transcription factor that bind to enhancer regions.
The operon model of the regulation of gene expression in bacteria was proposed by Jacob and Monod.
Other choices: Watson and Crick, Franklin, Darwin, Mendel
In 1961, Jacob and Monod proposed the operon model of gene expression.
Regulatory proteins bind to the operator.
Other choices: The lactose-utilization genes, the regulatory gene, RNA polymerase, transcription factors
Transcription is inhibited when a regulatory protein binds to the lac operon operator.
Translation & Transcription Notes
Types of RNA:
Messenger RNA (mRNA) → Carries DNA message from the nucleus to the ribosome.
Transfer RNA (tRNA) → Transfers amino acids to the ribosomes.
Ribosomal RNA (rRNA) → Along with proteins, makes up ribosomes.
Also 6 others, not necessary for this unit.
Transcription:
RNA is synthesized complementary to DNA
RNA has uracil base instead of thymine
RNA is made by RNA polymerase in the 5’ to 3’ direction
RNA is complementary to only one DNA strand → A gene is encoded on only one strand of DNA
Transcription Initiation:
RNA polymerase binds DNA at promoter
RNA polymerase unwinds DNA and begins making a complementary strand on one strand of the DNA
The promoter signifies which strand is the template (coding) strand
Transcription factors can make a promoter more or less active, regulating gene expression
RNA Modification:
Messenger RNA (mRNA) is used to make proteins
In eukaryotes, mRNA is modified in 3 ways:
5’ cap modified G to tell where to start translation
Poly A tail to 3’ end: 150-200 A to inhibit degradation
These structures aid in RNA stability and translation
Splicing
Cutting out the introns and putting together the exons
Splicing:
Introns = Non-coding DNA
Exons = Coding DNA
Splicing = Putting together the exons
Occurs in the nucleus before exiting to the cytoplasm
If genes make proteins but there are only 19,000 different genes in the human genome, how do we make the almost 100,000 necessary proteins in humans? → Alternative Splicing
Putting together the exons in different orders
The Genetic Code:
Each three base pairs of mRNA encodes an amino acid, a codon
This code is universal (virtually all organisms use the same code)
The code is redundant (The same amino acid may be encoded by multiple combinations of letters
Translation:
Once an mRNA is made, it is exported from the nucleus to the cytoplasm
Then, the making of a protein based on the information in the mRNA can begin
Ribosomes:
Large and small subunits, made of rRNA and protein
Small subunits bind to mRNA first
3 sites within the subunit:
A-Site → Acceptor side where tRNA enters
P-Site → Peptide bond forms between amino acids
E-Site → Exit of tRNA (gets released)
Transfer RNA:
tRNA contains an anticodon, a sequence of RNA bases that complements the codon sequence in the mRNA
Enzyme recognizes the anticodon of the tRNA and links the appropriate amino acid
Initiation of Translation:
Once ribosome has bound to mRNA, it slides along mRNA molecule until it reaches an AUG codon, which is the initiator codon
All proteins begin translation with a methionine amino acid
Translation Elongation:
Initiator codon occupies P-Site with tRNA bound on anticodon
The next codon occupies A-Site, tRNA with correct anticodon binds to codon in A-Site
Peptide bond formed between amino acids
Ribosome moves so tRNA from A-Site is now at P-Site
A new tRNA with anticodon is now bound at A-Site, next peptide bond formed
The initiator codon establishes the reading frame for the mRNA, codons do not overlap, once AUG is found it determines how a ribosome will translate that mRNA
Translation Termination:
Stop codon in A-Site causes release factor to release tRNA at the P-Site
Ribosome disassembles, polypeptide and mRNA released
Polyribosomes:
Many ribosomes may be translating a given mRNA
Modification:
There may be posttranslational modification of a polypeptide:
Addition of carbohydrate in Endoplasmic Reticulum/Golgi Apparatus
Addition of lipid
Cutting of polypeptide into functional units
Mutation:
A change in the genetic material, results in a change in protein
Point mutations → Change in a single base pair
Silent → Redundancy in code inserts the same amino acid at that position
Missense → Inserts another amino acid
Nonsense → Creates a termination codon, premature termination
Frame-Shift Mutations:
Causes a change in the reading frame of a message, rather than changing only one amino acid. This can drastically change the protein.
Insertion → Insertion of one or more bases
Deletion → Deletion of one or more base pairs