NOTE SET 9 (Exam 4 material)

Chapter 17 - RNA and Protein Synthesis

“From Gene to Protein”

Connection between genes and proteins

Synthesis and Processing of RNA

–Transcription

Synthesis of Protein

–Genetic Code

–Translation

Genetic Information

Stored in DNA

–the sequence of bases

–genes: scattered along chromosomes

Genetic info dictates synthesis of proteins

Proteins are the links between genotype (genetic makeup) and phenotype (appearance)

Connection between genes and proteins

Beadle and Tatum (and others previously)

–studied mutations in genes

–organism = Neurospora crassa (bread mold)

Auxotrophs - metabolic defects

–can grow on complete medium

–but not on minimal medium

–grow mutants on minimal medium with specific supplements

•(vitamin or amino acids)

–group based on growth characteristics

Beadle and Tatum’s Experiment

The one gene-one enzyme hypothesis

Beadle and Tatum’s Conclusions

Beadle and Tatum (and others previously)

–Altered genes = Altered enzymes (proteins)

–One gene - one enzyme hypothesis

Have altered the concept with time

–One gene - one protein.....TO:

–One gene - one polypeptide

Connection between genes and proteins

Central dogma of molecular genetics

DNA  RNA  protein

Overview of Transcription and Translation

Transcription

–Synthesis of RNA under the direction of DNA (DNA  RNA)

Translation

–Synthesis of a polypeptide by a ribosome under the direction of a mRNA (mRNA  protein)

Fig 17.3 Overview of Transcription & Translation

Txp and Txl are coupled in bacteria

Txp occurs in the nucleus in eukaryotes, while txl takes place in cytoplasm

Primary transcript (hnRNA) is modified (post-transcriptional modification) before being transported to cytoplasm.

Overview of Transcription and Translation

Prokaryotic / Eukaryotic differences

–Transcription and translation are coupled in prokaryotes

–Not coupled in eukaryotes - transcription in nucleus, translation in cytoplasm

–Eukaryotic mRNAs are processed; prokaryotic mRNAs are not.

Transcription

Messenger RNA (mRNA) is transcribed from the template strand of a gene

RNA polymerase

–separates or “melts” the DNA strands

–links the RNA nucleotides as they base-pair along the DNA template.

–adds nucleotides only to the 3’ end of the growing polymer

–gene (template strand) is read 3’5’, creating a 5’3’ RNA molecule

How does the RNA polymerase know where to start and stop transcription?

–more DNA in genome than that occupied by genes

Beginning and ending of gene

–marked in DNA by specific sequences

Promoter

–RNA polymerase binds and initiates transcription

–“upstream” of the information contained in the gene, the transcription unit

Terminator

–signals the end of transcription

RNA Polymerases

Bacteria

–single type of RNA polymerase that synthesizes all RNA molecules.

Eukaryotes

–three RNA polymerases (I, II, and III)

–RNA Pol II is used for mRNA synthesis.

Fig 17.7 Stages of Transcription

Fig 17.8 Promoters

In eukaryotes, proteins called transcription factors recognize the promoter region, especially a TATA box, and bind to the promoter.

After they have bound to the promoter, RNA polymerasebinds to transcription factors to create a transcriptioninitiation complex

Assembling theTranscription Complex

The first transcription factor (TF) to bind recognizes the TATA box Then other TFs can bind

Fig 17.8 Transcription Initiation Complex

Close-up of Transcription Elongation

•Polymerase unwinds helix

•Adds nucleotides that are complementary to bases in template strand

•Helix rewinds after RNA polymerase passes

•Many polymerase molecules can transcribe a single gene at the same time.

Transcription Termination

In prokaryotes

–specific sequence is terminator

–RNA pol stops right at sequence

In eukaryotes

–RNA pol continues for hundreds of nucleotides past the terminator sequence: AAUAAA

–another enzyme cuts the RNA 10 to 35 bases past the terminator sequence

RNA Processing in Eukaryotic Cells

Primary transcript (pre-mRNA or hnRNA) is modified before transport to cytoplasm

–5’cap

–polyA tail

–RNA splicing (removal of introns)

Eukaryotic mRNA Processing

5’ Cap

–modified form of guanine nucleotide

•Linked via 5’ --> 5’ phosphodiester bond

–Helps protect mRNA from degradation

–Important for translation initiation

•aids in ribosome binding

PolyA tail at 3’ end

–An enzyme adds 50-250 adenine nucleotides (poly A polymerase)

–Functions

•Protects from degradation

•Important for translation

•Facilitates export of mRNA from nucleus

RNA Processing: Splicing

–Eukaryotic Genes

•Composed of alternating exons and introns

•Exons

•expressed regions

•end up in final mRNA

•Introns

•intervening sequences

•removed from mRNA

Fig 17.10 RNA splicing

•Accomplished by a protein/RNA complex called - spliceosome

–consists of a variety of proteins and several small nuclear ribonucleoproteins (snRNPs)

–Each snRNP has several protein molecules and a small nuclear RNAmolecule(snRNA).

• Each is about 150 nucleotides long.

Fig 17.11 Role of snRNPs

Alternative RNA Splicing

•Gives rise to two or more different polypeptides, depending on which segments are treated as exons.

–Early results of the Human Genome Project indicate that this phenomenon may be common in humans.

Fig 17.12 Exons = Protein Domains

•Domains in proteins

•Discrete structural and functional regions

•Often encoded by distinct exons of gene

•May facilitate evolution via recombination between genes: “Exon Shuffling”

Overview of Translation

Genetic information stored as the nucleotide sequence is converted into an amino acid sequence

Read in groups of three nucleotides = Codons

THEFATCATATETHERAT

HEFATCATATETHERAT

EFATCATATETHERAT

Fig 17.4 The Triplet Code

mRNA is “read” in groups of three nucleotides,called “codons”

String of codons is an open reading frame (ORF)

AUG = txl start

UAA, UAG, or UGA = txl stop

64 possible codons - combinations of 3 bases

codons are read in a 5’  3’ direction

Each codon specifies which of the 20 amino acids will be incorporated

# of nucleotides is 3x the number of amino acids for a given coding region/protein sequence

# codons = # aa

Figuring out the Genetic Code

Marshall Nirenberg determined the first match in the early 1960s

UUU specifies phenylalanine

  • created artificial mRNA (all uracil bases)
  • translated by purified ribosomes in vitro
  • produced a polyphenylalanine

Other researchers and more elaborate techniques decoded the remaining codons

Fig. 17.5 The Genetic Code Dictionary

Characteristics of the Genetic Code

Universal

  • Essentially all organisms use the same genetic code dictionary

Degenerate

  • As many as six codons may specify the same amino acid - See Ser, Leu, Arg

Unambigous

  • A codon specifies only one amino acid

Summary

Genetic info encoded as sequence of non-overlapping base triplets, or codons

Each codon is translated into a specific amino acid during protein synthesis

Codons are read sequentially in a 5’3’ direction

Fig 17.13 Translation: The basic concept

tRNA transfers amino acids from the cytoplasm’s pool to a ribosome.

Each tRNA carries a specific amino acid at one end

Other end has a specific nucleotide triplet - anticodon that basepairs with codons in mRNA

Rribosome adds the growing polypeptide chain to the next amino acid carried by tRNA that is bound to the ribosome

Fig. 17.14 The Structure of tRNA

tRNA and Wobble Hypothesis

61 codons specify amino acids

But only about 45 tRNAs!!

Anticodons of some tRNAs can recognize two or more codons

U in anticodon can base pair with either A or G in codon

I (Inosine, a purine) in anticodon can basepair with U, C, or A in codon

Some anticodons can recognize two or more codons

U in anticodon can base pair with either A or G in codonAAU ---> UUG,UUA

I (Inosine) in anticodon can base pair with A, C, UCCI ---> GGA,GGC,GGU

Wobble Hypothesis

Affects basepairing of 3rd base of codon only

1st and 2nd base of codon follow Watson-Crick base pairing A=U, G=C

Fig 17.15 Joining of a specific amino acid to a tRNA by aminoacyl-tRNA synthetase

Amino acyl-tRNA synthetase links amino acid to specific tRNA

–20 different enzymes - one for each amino acids

Note: ATP hydrolyzed to AMP in “charging” tRNA with amino acid. Effectively, 2 ATP consumed

Fig 17.16 The anatomy of a ribosome

Each ribosome has binding site for mRNA and 3 binding sites for tRNAs

• P site holds tRNA thatcarries growing protein

• A site carries tRNA withnext amino acid to come in

• Discharged tRNAs leave ribosome at E site.

Comparison of Ribosomes

Stages of Translation

Initiation, Elongation, Termination

Fig 17.17 Initiation of translation

Start codon is AUG

Translation Elongation

Translocation

  • Ribosome moves the tRNA with the attached polypeptide from the A site to the P site (3 nucleotides or one codon)
  • Requires hydrolysis of GTP
  • tRNA still basepaired to mRNA, so mRNA also moves
  • tRNA in P site moves to the E site and then leaves the ribosome

Fig 17.18 Translation Elongation

Fig 17.19 Termination of Translation

Stop codon reaches A site

Release Factor binds to stop codon

Hydrolyzes bond between polypeptide and tRNA in P site

Translation complex disassembles

Fig 17.20 Polyribosomes

More than one ribosome may translate an mRNA at the same time, so many copies of a protein molecule may be obtained from one mRNA

Ribosomes and Translation

Ribosomes

Cytosolic

Membrane-bound - rough ER

Protein Secretion

rough ER --> Golgi --> Secretory Vesicles

What determines whether a cytosolic or rER-bound ribosome will translate an mRNA?

Signals for Protein Secretion

Signal peptide at start of coding region of polypeptide targets ribosome and mRNA to rER.

Fig 17.21 Signal Mechanism for Targeting Proteins to the ER

Signal Peptides

Other types of signal peptides target proteins to other organelles:

mitochondria

chloroplasts

nuclei

Multiple Roles for RNA in Cells

mRNAcarries info from DNA to ribosome

rRNAstructural and catalytic role in ribosome

tRNAadapter molecule in protein synthesis

1° transcriptfirst RNA - prior to processing or splicing

snRNAin spliceosomes - structural & catalytic

SRP RNAcomponent of signal recognition particle

Sno RNAAids in processing pre-rRNA

siRNA/miRNAinvolved in regulation of gene expression

Connection between genes and proteins

Genetic information is stored in DNA

As the nucleotide sequence

Proteins are the expressed form of the genetic information

Mutations

Changes in the genetic information in DNA

Altered nucleotide sequence

May affect proteins

Mutations in DNA

Point Mutations

change in just one base pair

basepair substitution

Frameshift Mutations

Due to loss of base pair(s)

Or addition of base pair(s)

Could lead to new codons (missense)

Mutations in DNA (see Fig 17.24)

Silent Mutation

point mutation that has no effect on protein sequence (generally in 3rd base of codon)

UGU (Cys) --> UGC (Cys)

Missense Mutation

point mutation that changes the amino acid

UGU (Cys) --> UGG (Trp)

Nonsense Mutation

amino acid codon altered to a stop codon

UGU (Cys) --> UGA (Stop)

Fig 17.23 The molecular basis of sickle-cell disease

Erythrocyte Phenotypes

Other Types of Mutations

Insertions/Deletions

Additions or losses of one or more nucleotide pairs

May causes a “frameshift” in the open reading frame (ORF)

Nucleotides read in new combinations of triplets - new codons

Fig 17.25 Consequence of bp deletion, insertion, codon insertion

Chapter 25 - The History of Life on Earth

Overview: Lost Worlds

The fossil record shows macroevolutionary changes over large time scales including

The emergence of terrestrial vertebrates

The origin of photosynthesis

Long-term impacts of mass extinctions

Conditions on early Earth made the origin of life possible

Chemical and physical processes on early Earth may have produced very simple cells through a sequence of stages:

1. Abiotic synthesis of small organic molecules

2. Joining of these small molecules into macromolecules

3. Packaging of molecules into “protobionts”

4. Origin of self-replicating molecules

Synthesis of Organic Compounds on Early Earth

Earth formed about 4.6 billion years ago, along with the rest of the solar system

Earth’s early atmosphere likely contained water vapor and chemicals released by volcanic eruptions (nitrogen, nitrogen oxides, CO2, methane, ammonia, hydrogen, hydrogen sulfide)

A. I. Oparin and J. B. S. Haldane hypothesized that the early atmosphere was a reducing environment

Stanley Miller and Harold Urey conducted lab experiments that showed that the abiotic synthesis of organic molecules in a reducing atmosphere is possible

The experiments of Stanley Miller (chapter 4) and others have shown that “reducing environments” rich in amino acids, nucleic acids, lipids, and carbohydrates would have been abundant on primordial earth.

However, the evidence is not yet convincing that the early atmosphere was in fact reducing

Instead of forming in the atmosphere, the first organic compounds may have been synthesized near submerged volcanoes and deep-sea vents

Amino acids have also been found in meteorites

Abiotic Synthesis of Macromolecules

Small organic molecules polymerize when they are concentrated on hot sand, clay, or rock

Protobionts - aggregates of abiotically produced molecules surrounded by a membrane or membrane-like structure

Protobionts exhibit simple reproduction and metabolism and maintain an internal chemical environment

Experiments demonstrate that protobionts could have formed spontaneously from abiotically produced organic compounds

e.g. small membrane-bounded droplets called liposomes can form when lipids or other organic molecules are added to water

Self-Replicating RNA and the Dawn of Natural Selection

First genetic material probably RNA, not DNA

RNA molecules called ribozymes have been found to catalyze many different reactions

e.g., ribozymes can make complementary copies of short stretches of their own sequence or other short pieces of RNA

Early protobionts with self-replicating, catalytic RNA would have been more effective at using resources and would have increased in number through natural selection

Early genetic material might have formed an “RNA world”

First Single-Celled Organisms

Oldest known fossils are stromatolites, rock-like structures composed of many layers of bacteria and sediment

Stromatolites date back 3.5 billion years

Prokaryotes were Earth’s sole inhabitants from 3.5 to about 2.1 billion years ago

Photosynth & the O2 Revolution

Most atmospheric O2 is of biological origin

O2 produced by oxygenic photosynthesis reacted with dissolved iron and precipitated out to form banded iron formations

Source of O2 likely bacteria similar to modern cyanobacteria

~2.7 billion years ago, O2 began accumulating in atmosphere and rusting iron-rich terrestrial rocks

This “oxygen revolution” (2.7 to 2.2 billion years ago)

Posed a challenge for life

Provided opportunity to gain energy from light

Allowed organisms to exploit new ecosystems

The First Eukaryotes

The oldest fossils of eukaryotic cells date back 2.1 billion years

The hypothesis of endosymbiosis proposes that mitochondria and plastids (chloroplasts and related organelles) were formerly small prokaryotes living within larger host cells

An endosymbiont is a cell that lives within a host cell

The prokaryotic ancestors of mitochondria and plastids probably gained entry to the host cell as undigested prey or internal parasites

In the process of becoming more interdependent, the host and endosymbionts would have become a single organism

Serial endosymbiosis supposes that mitochondria evolved before plastids through a sequence of endosymbiotic events

Key evidence supporting an endosymbiotic origin of mitochondria and plastids:

Similarities in inner membrane structures and functions

Division is similar in these organelles and some prokaryotes

These organelles transcribe and translate their own DNA

Their ribosomes are more similar to prokaryotic than eukaryotic ribosomes

The Origin of Multicellularity

The evolution of eukaryotic cells allowed for a greater range of unicellular forms

A second wave of diversification occurred when multicellularity evolved and gave rise to algae, plants, fungi, and animals

Earliest Multicellular Eukaryotes

Comparisons of DNA sequences date the common ancestor of multicellular euk. to 1.5 billion yrs ago

Oldest known fossils of multicellular eukaryotes are of small algae that lived ~1.2 billion yrs ago

The “snowball Earth” hypothesis suggests that periods of extreme glaciation confined life to the equatorial region or deep-sea vents from ~750- 580 million yrs ago

The Cambrian Explosion

The Cambrian explosion refers to the sudden appearance of fossils resembling modern phyla in the Cambrian period (535 to 525 million years ago)

The Cambrian explosion provides the first evidence of predator-prey interactions

So does that mean all life came from ONE original cell?
Not exactly, but all 3 domains of life probably had a
“last universal common ancestor”

The first organism was probably an RNA-based (rather than DNA) life form with extensive amounts of horizontal genetic transmission (viral infection?) between cells. The evolution of a reverse transcriptase or transposon-like activities may have converted the RNA based life form into DNA-based cell types--at least 3 types of which survive today.