OVERVIEW

The course explains the molecular mechanisms of information management in prokaryotic and eukaryotic cells. The acquisition of knowledge on this topic is necessary to understand the multiple functions of living beings, the dynamic of their evolution, the basis of pathology and the molecular keys of their adaptation to the different environments on the planet. The course is completed with the theoretical and practical study of the main investigation techniques for genomes and related transcripts

AIMS AND CONTENT

LEARNING OUTCOMES

The teaching aims to provide the students with the basic knowledge on the  main molecular mechanisms of information management by the cell. The structural and evolutionary characteristics of nucleic acids, their interactions with the proteins involved in the processes of replication, transcription and translation in different organisms, from viruses to multicellular eukaryotes, will be illustrated. The main control and regulation mechanisms of gene expression in prokaryotes and eukaryotes will also be illustrated with specific insights on the action of transcription factors and regulatory RNAs in their respective functional contexts. The aim of the course is also to provide theoretical knowledge of the main recombinant DNA techniques including, DNA amplification (PCR), gene cloning, DNA and RNA sequencing, the main study approaches and genome analysis and some basic principles of synthetic biology. Finally, will be possible to acquire practice through by specific laboratory activity.

AIMS AND LEARNING OUTCOMES

The course has the specific purpose of allowing the student to acquire the basic knowledge on on molecular biology. The acquisition of the required credits will be accomplished with the demonstration of an in-depth knowledge of the mechanisms underlying the processes of replication, transcription and translation of genetic information, as well as detailed information on the structural organization of nucleic acids, mechanisms of recombination and transposition and on the multiple functions of RNA. The students will also possess a clear and in-depth knowledge of the role of the genetic code as a universal information management system in living beings.

The course will also enable the acquisition of information relating to the main techniques currently used for the study of the genome, such as PCR and quantitative PCR, nucleic acid sequencing and DNA chip and their relative applications in various professional fields (research, medical diagnostics, forensic medicine, monitoring of environmental and food quality) in addition to the basic techniques for the creation of libraries, cDNA library and the main techniques for recombinant DNA management

The expected practical activity will also make the student able to autonomously manage the main laboratory techniques currently employed for the extraction and electrophoretic analysis of DNA, for obtaining cDNA from messengers extracted from eukaryotic cells, for their amplification to PCR medium and for the subsequent electrophoretic analysis of the results.

PREREQUISITES

To approach in the most profiteable way the study of molecular biology, it is necessary to have acquired the knowledge of general and inorganic chemistry (in particular the basic concepts of chemical thermodynamics, chemical equilibria, pH), of organic chemistry (in particular a strong knowledge of the main classes of organic molecules and in-depth knowledge of the four classes of biological macromolecules) and biochemistry (in particular it requires a thorough knowledge of the structure of proteins, of the concept of enzymatic catalysis, of the main processes of metabolism).

TEACHING METHODS

Lectures and seminars

Practical activities

Students who have valid certification of physical or learning disabilities on file with the University and who wish to discuss possible accommodations or other circumstances regarding lectures, coursework and exams, should speak both with the instructor and with Professor Sara Ferrando (sara.ferrando@unige.it), the Department’s disability liaison.

SYLLABUS/CONTENT

DNA structure. 
Gene concept.
Chromatin and histones, the nucleosome and topoisomerases
Molecular mechanisms of DNA replication in prokaryotes and eukaryotes. The DNA polymerases of prokaryotes and eukaryotes (structure, functions, nuclease activity), DNA primase, helicase. The control of fidelity of replication.
The Okazaki fragments, the RNAse H; 
the DNA ligase. 
The mechanisms of beginning of replication in prokaryotes and eukaryotes, DNA A, the Replicator, the initiator, the role of CDk in controlling the beginning of replication.
The end of replication in prokaryotes and eukaryotes; topoisomerase in bacteria and telomerase in eukaryotes.
Transcription in prokaryotes and eukaryotes: promoters; transcription factors in bacteria; the RNA polymerases of prokaryotes and eukaryotes; the moderator; the termination of the transcription; the overall management of transcription in living beings.
The maturation of the messenger in eukaryotes; capping in 5 ’, polyadenylation; autosplicing of type I and II introns; splicing managed by the spliceosome; alternative splicing
The rRNA; tRNA synthesis. The synthesis of aminoacyl tRNA and aminoacyl tRNA synthetases.
The genetic code.
Translation in prokaryotes and eukaryotes.
Post-transcriptional regulation of gene expression, regulatory RNAs in bacteria; riboswitches, RNAi, the molecular basis of RNA interference; the micro RNA.
Specific site recombination and recombinases. VDJ recombination.
Homologous recombination.
DNA transposons.
Retrotransposons. The SINES and the demonstration of their origin from retrotransposons.
The synthesis of oligonucleotides.

Nucleic acid extraction techniques from different biological samples. Qualitative and quantitative analysis techniques of nucleic acids. Electrophoresis on agarose gel and in micro-fluidics. Spectrophotometric and fluorometric assays. Polymerase chain reaction (PCR) principle and applications, primer design software. Special applications of PCR. RNA reverse transcription, cDNA and RACE techniques. Site-specific mutagenesis. Quantitative PCR (qPCR) and digital PCR (ddPCR) principles and applications. Restriction enzymes and restriction maps, enzyme research software. Creation of recombinant DNA. Vectors and gene cloning. Use of probes for the study of DNA, genomic and cDNA libraries, microarrays. DNA sequencing techniques. Chemical method Sanger enzymatic method Next generation DNA sequencing (NGS) techniques. Illumina method and 454 method. Satellite DNA and its uses in forensic genetics. DNA testing and paternity testing. Mitochondrial DNA and chloroplast DNA: replication, functional and structural characteristics. The use of mitochondrial DNA in the study of evolution. Mitochondrial Eve. Y-Adam. The use of mitochondrial DNA in forensic genetics. Synthetic biology. The definition of a minimal bacterial genome; the creation of the first artificial microorganism. The antisense approach. Antisense oligonucleotides; the PNAs Xenobiology: The expansion of the genetic code. The use of the Amber codon for the insertion of non-natural amino acids into proteins; orthogonal tRNAs and related synthetases Orthogonal ribosomes; the production of alien proteins; XNAs, the XNA-DNA relationship

Practical part (1CFU):

Extraction of nucleic acids from biological samples Electrophoretic analysis of DNA on agarose gel Reaction setup for reverse transcription and PCR reactions Nucleic acid assay Digestion with restriction enzymes

RECOMMENDED READING/BIBLIOGRAPHY

The in depth analysis of the contents of the program can be carried out on any university textbook on molecular biology offered by the market, as long as they are editions updated to the last five years.

TEACHERS AND EXAM BOARD

Exam Board

MARCO GIOVINE (President)

SONIA SCARFI'

MARINA POZZOLINI (President Substitute)

LESSONS

LESSONS START

beginning of October

Class schedule

MOLECULAR BIOLOGY AND LABORATORY

EXAMS

EXAM DESCRIPTION

The student will be evaluated through a final oral test (max 30 points and possible honors). The student can increase the grade obtained in the oral exam through the contribution given by the evaluation of the practical and laboratory activity (max 1 points). In any case, the maximum exam score is 30 points and possible honors

ASSESSMENT METHODS

The final evaluation of the training course will be carried out through an oral test, to whose evaluation the score previously acquired in the practical part (max 2/30) will be added. The maximum possible score is 30 cum laude. The oral examination requires, for each student, to be examined by at least two members of the commission and to answer at least three questions relating to the topics listed in the program. To pass the exam, the student must demonstrate to have acquired at least sufficient knowledge on each of the three topics covered. The final evaluation will take into account the level of knowledge of the contents as well as the expository and reasoning skills demonstrated in the discussion conducted on the requested topics. To this will be added the evaluation of the practical and laboratory activities. The latter will derive from the sum of the score obtained in the following 3 activities: short entry test to practical exercises concerning the preparatory topics for practical activities carried out in the laboratory just before starting the activity (max 0.5 points), practical laboratory activity (max 0.5 points), short test to verify bioinformatics skills carried out in the classroom (max 1 point). In case of final laboratory score <1, the student will have to answer an additional question on the laboratory part.