the lac operon. in bacteria, the genes involved in the same process are often clustered together....

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The lac operon

• In bacteria, the genes involved in the same process are often clustered together. For example, the genes that allow E. coli to break down milk sugar (lactose) to produce energy.

Lactose catabolism

• lacY encodes lactose permease -transports lactose into the cell

• lacZ encodes -galactosidase – enzyme that catalyses the reaction: lactose glucose + galactose

• lacA encodes lactose transacetylase – biological function unclear.

Lactose catabolism

• These genes are controlled. E. coli is a successful competitor in the gut because it doesn’t waste time and energy making mRNA and proteins that are not needed. The lac genes are only transcribed if lactose is present in the growth medium.

• These genes are expressed co-ordinately. Either they are all switched on or they are all switched off.

Lactose catabolism

• The coordinate regulation arises from the clustering of the genes (strictly called CISTRONS) into a structure called an OPERON.

• There is also a regulatory gene, the lacI gene, that is not part of the operon. This produces a repressor protein that controls the operon.

Lactose catabolism

Transcription

translation

-galactosidase enzyme

lactose permease

lactose trans-

acetylase

DNA

mRNA

protein

(polycistronic message)

lactose

LacIrepressor

Inactive repressor-effector complex

RNA polymerase

Active repressor binds

to operator

The lac operon

P lacI P lacO lacZ lacY lacA

Transcription

translation

-galactosidase enzyme

lactose permease

lactose trans-

acetylase

DNA

mRNA

protein

(polycistronic message)

lactose

LacIrepressor

Inactive repressor-effector complex

RNA polymerase

Active repressor binds

to operator

The lac operon

P lacI P lacO lacZ lacY lacA

The three coding sequences lie side by side but there is only one promoter

Transcription

translation

-galactosidase enzyme

lactose permease

lactose trans-

acetylase

DNA

mRNA

protein

(polycistronic message)

lactose

LacIrepressor

Inactive repressor-effector complex

RNA polymerase

Active repressor binds

to operator

The lac operon

P lacI P lacO lacZ lacY lacAThis means that there is only one mRNA that encodes three proteins. Each coding region has its own start and

stop codon

Transcription

translation

-galactosidase enzyme

lactose permease

lactose trans-

acetylase

DNA

mRNA

protein

(polycistronic message)

lactose

LacIrepressor

Inactive repressor-effector complex

RNA polymerase

Active repressor binds

to operator

The lac operon

P lacI P lacO lacZ lacY lacA

The separate lacI gene is not controlled. It hasIts own promoter and encodes a repressor

protein. It is not part of the operon

Transcription

translation

-galactosidase enzyme

lactose permease

lactose trans-

acetylase

DNA

mRNA

protein

(polycistronic message)

lactose

LacIrepressor

Inactive repressor-effector complex

RNA polymerase

Active repressor binds

to operator

The lac operon

P lacI P lacO lacZ lacY lacA

In the absence of lactose, the repressor

protein binds to a special site in the operon called the OPERATOR and

prevents RNA polymerase from moving along the

DNA

Transcription

translation

-galactosidase enzyme

lactose permease

lactose trans-

acetylase

DNA

mRNA

protein

(polycistronic message)

lactose

LacIrepressor

Inactive repressor-effector complex

RNA polymerase

Active repressor binds

to operator

The lac operon

P lacI P lacO lacZ lacY lacA

In the presence of

lactose (effector), the

repressor protein

binds to the lactose

and changes shape. It

now falls off the

operator and RNA

polymerase can

transcribe the operon

DNA

LacIrepressor

RNA polymerase

Active repressor binds

to operator

Lactose absent: operon switched off

The lac operon

mRNA

P lacI P lacO lacZ lacY lacA

Transcription

translation

-galactosidase enzyme

lactose permease

lactose trans-

acetylase

DNA

mRNA

protein

(polycistronic message)

lactose

LacIrepressor

Inactive repressor-effector complex

RNA polymerase

P lacI P lacO lacZ lacY lacA

The lac operon

François Jacob and Jacques Monod worked out how the lac operon functioned and they formulated the operon hypothesis.

Jacob

Monod

Jacob and Monod

The lac operon

The properties of various mutants allowed Jacob and Monod to work out how operons work.

lac mutants

The lac operon

P O lacZ lacY lacA

Active -galactosidase enzyme

DNA

mRNA

protein

DNA

DNAX

XX

mRNA

protein

lacZ mutations are recessive

The lac operon

Lactose catabolism

• Mutants where the lacI gene has mutated, will grow on lactose.

• However they make β-galactosidase all of the time. These mutants that have lost the ability to control gene expression are called constitutive mutants. They are also recessive.

Constitutive mutants

The lac operon

DNA

LacIrepressor

RNA polymerase

Active repressor binds to both operators

X

XNo active

repressor to bind to

operator

P lacI P lacO lacZ lacY lacA

P lacI P lacO lacZ lacY lacA

The lac operon

lacI mutations are recessive

• Jacob & Monod realised that if their operon hypothesis was right, there should be another type of constitutive mutant – one where the operator has mutated so that the repressor cannot recognise it.

• Such mutants should be dominant and it should be possible to isolate them in a diploid.

A testable prediction

The lac operon

DNA

mRNA

LacIrepressor

RNA polymerase Active repressor binds only

to wild type operator

X DNA

lacOc mutations are dominant

The lac operon

P lacI P lacO lacZ lacY lacA

P lacI P lacO lacZ lacY lacA

• Jacob & Monod mutated a diploid wild type to see whether they could get constitutive mutants.

• They did get them, and showed that they

mapped to the operator region.

This supported their hypothesis.

The lac operon

The lac operon

The lac repressor is an example of a negative regulatory protein, whose action prevents expression of the genes under its control and whose function is controlled by an effector molecule (in this case, lactose).

The lac operon

Catabolic repression

The lac operon is also under the control of a positive regulatory protein.

E. coli’s preferred carbon source is glucose.

Glucose inhibits transcription of the lac operon, even in the presence of lactose.

Inhibition occurs in lacI and lacO mutants, as well as wild type, indicating the effect of glucose is NOT via the repressor-operator interaction.

The lac operon

The effect of glucose is mediated by a nucleotide, cyclic AMP (cAMP).

The intracellular concentration of cAMP is high in the absence of glucose and low in its presence.

cAMP binds to a catabolic activator protein (CAP), upstream of the lac promoter driving the lac operon.

When bound to cAMP, CAP enhances lac transcription.

Transcription

translation

-galactosidase enzyme

lactose permease

lactose trans-

acetylase

DNA

mRNA

protein

(polycistronic message)

Glucose

RNA polymerase

The lac operon

P lacO lacZ lacY lacA

cAMP

CAP

The lac operon

Regulation of expression of the lac operon is under two sets of controls, both of which are governed by environmental factors.

The repressor-operator interaction provides an “all or none” level of control (lactose on).

[CAP-cAMP]-CAP-binding site interaction provides a modulatory control.

(glucose levels control rate of mRNA initiation)

Summary

Complementation

• Diploid, Haploid• Dominant, Recessive• Homozygous, Heterozygous• Cistron• Cross-feeding

Colinearity of the gene and protein

Protein structure Haemoglobin Genetic code amino acid sequence

The Genetic code

Codon Dictionary of the genetic code How the code was deciphered How the code works

tRNA and Translation

RNA translation (5' 3') Ribosomes Structure of tRNA Anticodon Mechanism of translation Wobble hypothesis

Inosine (I) is a rare base found in tRNA, often in the anticodon, capable of binding to adenine, uracil or cytosine.

RNA Translation

RNA growth (5' 3') RNA polymerase, structure and properties Promoter, consensus Mechanism of translation Termination

Suggested reading

Regulation of gene transcription (2000) In: An Introduction to Genetic Analysis. pp 336-344. Griffiths, A. J. F,. Miller, J. H., Suzuki, D. T., Lewontin, R. C. and Gelbart, W. M. (Eds). Freeman and Company, New York.

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