Cellular Processes
Gene Regulation
DNA Packaging
Think of "beads on a string"
Histone core: a protein that bind the DNA twice
Different types of Histones: H1, H2A, H2B, H3, H4
Only the H2A, H2B, H3, H4 form the histone core. The H1 is outside and not apart of the code.
Nuclesomes are formed when the DNA wraps around the histones twice.
Nuclesomes are strung together like beads on a string by linker DNA.
Interactions between nucleosomes cause the thin fiber to coil or fold into this thicker fiber.
The tight helical fiber needs help of the H1 which is outside the nucleosome.
The 30-nm fiber forms looped domains that attach to proteins.
The looped domains coil further.
The DNA is packaged with proteins in an elaborate complex known as chromatin (the basic unit of the nucleosome).
Prokaryotes
In prokaryotes, genes are organized as operons.
Multiple genes are controlled by the same promoter.
Operator is not in Eukaryotes it is in Prokarytoes
Lac Operon
Lactose operon is an operon required for the transport and metabolism of lactose in bacteria.
Lac Z is a gene that forms mRNA
Enzymes responsible is galactosidase
Lac Y takes in the lactose
Enzymes responsible is permase
Lac A adds an acidicyl group to lactose
Enzyme responsible is transacetylase
Lac I is the lac repressor (regulatory gene)
Can switch off the operon when binding to the operator and it is active by itself.
Operon is off!
Lactose is absent, repressor is on(repressor binds to the operator), opreron is off
Operon is on!
Lactose is present, repressor is inactive(allolactose inactive the repressor), operon on
cAMP Levels
Lactose is present, glucose is absent, cAMP levels are high and the CAP is activated
Lactose is present, glucose is present, cAMP levels are low and CAP is inactivated
Tryptophan
an amino acid
A negative regulator because it binds to a repressor
When tryptophan is absent, the repressor is inactivated which means it can't bind to the operator,operon is on
When tryptophan is present, the repressor is active which means it can bind to the operator, operon is off
Transcription Factors
General transcription factors leads to low(basal) levels of transcription
Repressor binds to the enhancer sequence and bends but prevents RNA poly II to bind
Proximal control elements are sequences in DNA close to promoter
allows RNA pol II to bind weakly
Transcription factors binds to the proximal elements and transcription is low level
Specific transcription ,like activators, lead to increased expression (high levels of transcription)
Activators bind to the enhancer sequence and bends the sequence
Distal control elements are enhancers that are located upstream or downstream of a gene
Cell Signaling
3 Stages of Cell Signaling
Reception: A signal molecule binds to a receptor protein located at the cell's surface.
Transduction: The receptor protein changes in some kind of way when the signaling molecule binds to it. The signal is conveyed to a form that can bring about a specific cellular response. Transduction usually occurs in a series of steps-signal transduction pathway.
AKA: Amplification (involves Second Messengers)
Cellular Response: The transduced signal triggers a cellular response
Types of Cell Signaling
Local Signaling
Paracrine Signaling
Involves direct signaling: affects nearby cells
Synaptic Signaling
Neurotransmitters released which diffuses across the synapse, stimulating the target cell.
Long-Distance Signaling
Exocrine/Hormonal Signaling
Hormone must travel through the blood stream
Types of Signal Molecules
Hydrophobic Signal Molecule
Receptor in Cell Cytoplasm
Receptor in Cell Nucleus
Hydrophobic Signal Molecule
Receptor on/in Cell (Plasma) Membrane
Membrane Receptors
G protein coupled receptor
A cell surface transmembrane receptor that works with the help of a G protein.
Tyrosine kinase receptor
Allows for the transfer of phosphate from ATP to the tyrosine kinase regions of a dimer, once a signal molecule binds to it.
Ion channel receptor
A membrane-bound receptor which undergoes a conformational change once the signal molecule attaches to the receptor. Allows for the passage of ions.
Cellular Components
Phospholipid Bilayer
A membrane made up of two fatty acid
tails and a hydrophillic head.
Fatty Acids (Fats)
Triglycerides (Fats)
Saturated
Unsaturated
Oils
Present in plants, a layer of cellulose
and chitin which protects the cell.
Lipids
Glycerol
Mitochondria
Supplies energy to the cell through various cellular processes
Cell Wall
A protective wall that is made
from cellulose and chitin
Cytoplasm
An aqueous solution where the
cellular components reside in.
Vacuole
Contains water or
various liquids in the cell.
Central Vacuole
Food Vacuole
Nucleus
The component of a cell which
contains the genetic material of a cell.
Lysosome
A vesicle which breaks down
molecules and recycles them.
Endocytosis
Receptor Mediated
Phagocytosis
Pinocytosis
Ribosomes
Synthesizes proteins, made of RNA and proteins.
free or bound
proteins
Endoplasmic Reticulum
Focuses on synthesizing protein (rough) and lipids (smooth).
Smooth ER
Rough ER
Golgi Apparatus
Gives instructions to proteins and transports them
Gene Expression
2. Elongation Cycle of Translation
1. Codon Recognition
Anticodon of aminoacyl tRNA base pairs with complementary mRNA codon in A site. Hydrolysis of GTP is present in this step. The aminoacyl tRNA with the appropriate anticodon binds and proceeds with the cycle.
2. Peptide Bond Formation
3. Translocation
Ribosome translocates tRNA in the A site to the P site. The empty tRNA in the P site is moved to the E site where it gets released. The mRNA moves with its bound tRNAs, which bring the next codon to the A site so it can be translated.
Translation
Molecule of mRNA is moved in a ribosome where codons are translates into amino acids. tRNA molecules interpret each type of nucleotide in sets of 3. A tRNA adds its amino acid to a growing polypeptide chain once the anticodon hydrogen bonds to the complementary codon on the mRNA.
1. The Initiation of Translation
1. A small ribosomal unit binds to an mRNA molecule. Then, an initiator tRNA, with anticodon UAC, pairs with the start codon, AUG, which carries the amino acid methionine (Met).
2. A large ribosomal subunit arrives to complete the initiation complex. The initiation factors are in charge of connection all the translation components. Hydrolysis of GTP gives off energy to the assembly. The initiator tRNA is in the P site while the A site is free for the tRNA who carries the next amino acid.
An rRNA molecule of a large ribosomal subunit catalyzes the formation of a peptide bond. This step removes the polypeptide from tRNA in the P site and attaches it to the amino acid on the tRNA in the A site.
1. A ribosome reached the stop codon and the A site of the ribosome accepts a "release factor".
3. Termination of Tranlastion
2. The release factor promotes hydrolysis of the bond between tRNA in P site and the last amino acid. Therefore, it frees the polypeptide from ribosome.
3.The two ribosomal subunits and the other parts dissociate.
3 Steps of Transcription
1. The initiation of Transcription
RNA polymerase binds to the promote, the DNA strands unwind, and the polymerase initiates RNA synthesis at the start point on the template strand
Eukaryotes
1. The eukaryotic promoter has a TATA box which is a nucleotide sequence containing TATA.
2. Transcription factors bind to the DNA before RNA polymerase II can bind to it.
3. Other transcription factors bind to the DNA along with RNA polymerase II, forming the transcription initiation complex.
Elongation
The polymerase moves downstream, unwinding the DNA and elongating the RNA transcript in 5' to 3' direction.
Termination
The RNA transcript is release and the polymerase detaches from the DNA
RNA Modifications after Transcription in Eukaryotic Cells
5' Cap and Poly A Tail
A 5' cap and a Poly A tail are added to the two ends of a eukaryotic pre-mRNA molecule in order to 1.) facilitate the export of mature RNA from the nucleus 2.) protect the mRNA from degrading 3.)help ribosomes attach to the 5' end of the mRNA when it is in the cytoplasm.
RNA Splicing
During RNA processing, the introns are cut out and the eons are spliced together.
DNA Replication
Enzymes of DNA and their Functions
Helicase
Unwinds parental double helix at replication forks
Primase
Creates RNA primer and places one at 5' end of leading strand and several on lagging strand
DNA Pol III
Synthesizes new DNA strands by adding nucleotides to 3' end of RNA primer
DNA Pol I
Removes RNA primer and replaces it with DNA
Ligase
Connects fragments of DNA
Topoisomerase
Prevents DNA from "overwinding" by releasing tension ahead of the replication
DNA Synthesis
Leading Strand
Synthesizes in a direction toward the replication fork
Lagging Strand
Synthesizes in a direction away from the fork
Replication Fork
point at which the two DNA strands begin to separate for replication
Origin of Replication
the point in the DNA at which replication begins
Cell Division
Cell Communication
Cells Signal one another frequently to tell other cells to begin replication, beginning at the phospholipid-bilayer.
This involves the Phospholipid-bilayer; where signal molecules activate cellular process, beginning with the attachment to a receptor.
Structure of DNA
Semi-Conservative Nature of DNA
DNA was discovered to be Semi-Conservative though the experiments by Messleson and Stahl. Both strands of parental molecule separate and each template synthesizes a new, complementary strand.
Complementary Bases
Adenine
Thymine
Guanine
Cytosine
Three Steps of DNA Replication
Initiation
Replication begins at the ORI, where helices begins to unwind the DNA. Topoisomerase releases tension ahead of the replication fork. The RNA primers are created to begin elongation.
Elongation
The primer begins the leading strand. The existing strand is now the template strand. DNA polymerase III begins putting down the new bases. The lagging strand is synthesized in okazaki fragments. DNA ligase puts together the okazaki fragments.
Termination
DNA polymerase I removes the RNA bases from the 5' end