Integrated tutorials in biochemistry and molecular genetics

lbio1322  2019-2020  Louvain-la-Neuve

Integrated tutorials in biochemistry and molecular genetics
Note from June 29, 2020
Although we do not yet know how long the social distancing related to the Covid-19 pandemic will last, and regardless of the changes that had to be made in the evaluation of the June 2020 session in relation to what is provided for in this learning unit description, new learnig unit evaluation methods may still be adopted by the teachers; details of these methods have been - or will be - communicated to the students by the teachers, as soon as possible.
5 credits
0 h + 60.0 h
Q2
Teacher(s)
Hallet Bernard; Soumillion Patrice;
Language
French
Main themes
From the phenotype to the gene and from the gene to the protein, the formation covers different approaches used to identify and isolate a gene, to modify its sequence, to study its function, and to characterise its product. It illustrates the concepts of DNA cloning, the structure-function relationship of proteins and of retro-genetics, by making use of DNA recombinant techniques (restriction, ligation, PCR, sequencing, transformation, etc), mutagenesis, purification and enzymatic characterisation of proteins.
Aims

At the end of this learning unit, the student is able to :

1 The tutorials constitute a practical and theoretical initiation to the general procedures in modern genetics, combining molecular biology and biochemical techniques. Starting from real problems, they aim to familiarize the student with the design of experimental approaches and the interpretation of the results.
 

The contribution of this Teaching Unit to the development and command of the skills and learning outcomes of the programme(s) can be accessed at the end of this sheet, in the section entitled “Programmes/courses offering this Teaching Unit”.
Content
The major part of the activity consists in a laboratory work (45h) close to real research situation, from mutagenesis of a gene of interest to the phonotypical and biochemical characterization of the mutated gene product. Manipulation steps include the mutagenesis of a cloned DNA fragment, the identification of the mutants of interest, the sub-cloning of mutated genes, the sequencing of mutations, purification of the mutated proteins and measurement of their enzymatic activity. Results are interpreted in terms of structure-function relationship changes in the enzyme based on protein structure modelling software. In the accompanying seminars (15h), theoretical aspects of the practical work are discussed, and an overview is given on the basic methods of molecular biology (PCR, gene cloning, DNA sequencing, mutagenesis, protein expression and purification etc.)
Evaluation methods
Experimental part of the exercises: Poster presentation summarizing the results obtained in laboratory.
Seminars part: A written exercise in which student have to solve a basic problem of genetic engineering. Students may have access to all information they would need (articles, notes, powerpoints, etc.) to solve the problem.
Other information
Precursory courses: Basic formation in molecular genetics, microbiology, cellular biology and biochemistry, (level BIO12-BIO13)
Support
  • Experimental part of the exercises: -Textbook and protocols explaining the manipulation performed in laboratory.
  • Seminars -Powerpoint files available on moodle
Teaching team: Teaching assistants in molecular biology and biochemistry with punctual intervention of main teachers
Faculty or entity
BIOL


Programmes / formations proposant cette unité d'enseignement (UE)

Title of the programme
Sigle
Credits
Prerequisites
Aims
Master [120] in Biochemistry and Molecular and Cell Biology