Épissage constitutif et alternatif. A) Schéma d’un événement d’épissage. L’intron excisé mène à la production d’un ARNm mature qui est exporté au cytoplasme. d’une dizaine d’éléments contrôlant l’épissage alternatif des exons mutuellement exclusifs IIIb et IIIc de FGFR2 ont été identifiés (figure 3A). Bien que les. Causes d’altération de l’épissage alternatif dans les cancers. A) Mutations affectant l’épissage alternatif et quelques exemples de gènes ayant subi ce type de.

Author: Mauk Megal
Country: Belgium
Language: English (Spanish)
Genre: Photos
Published (Last): 12 May 2013
Pages: 94
PDF File Size: 3.79 Mb
ePub File Size: 14.3 Mb
ISBN: 597-8-87012-179-2
Downloads: 42183
Price: Free* [*Free Regsitration Required]
Uploader: Yozshuzuru

A collection of writing tools that cover the many facets of English and French grammar, style and usage. Most of protein-coding human genes are subjected to alternative pre-mRNA splicing. The generation of two or more different mature mRNA’s alternaif the same primary transcript through variation in the sites of splicing. Glossaries and vocabularies Access Translation Bureau glossaries and vocabularies.

Current usage metrics About article metrics Return to article.

Alternative splicing and tumor progression

This mechanism is highly regulated to precisely modulate detection of specific splice sites. These splicing sequences make splicing susceptible to polymorphisms and mutations. Services Articles citing this article Alterantif 2. Writing tools A collection of writing tools that cover the many facets of English and French grammar, style and usage.


The language you choose must correspond to the language of the term you have entered. Med Sci Paris ; Splicing factors and spliceosome components recognize splicing signals and regulatory sequences of the pre-mRNAs.

Search Site only in current section.

Presentation — Laboratoire de Biologie et Modélisation de la Cellule

Issue Med Sci Paris. Examples of associations between human rare diseases and defects in pre-messenger RNA splicing are accumulating.

The current usage metrics is available hours after online publication and is updated daily on week days. FAQ Frequently asked questions Display options.

Data correspond to usage on the plateform after Access a collection of Canadian resources on all aspects of English and French, including quizzes. This novel class of alternative 3′-terminal exons are downregulated on a large scale by doxorubicin, a cytostatic drug targeting topoisomerase II, and play a role in cell cycle regulation, including centromere-kinetochore assembly.

Epidsage growing of knowledge regarding splicing regulation, several approaches have been developed to compensate alteenatif the effect of deleterious mutations and to restore sufficient amounts of functional protein.

Previous article Next article.

Link to PubMed entry. Info A recently evolved class of alternative 3′-terminal exons involved in cell cycle regulation by topoisomerase inhibitors.

Change the order of display of the official languages of Canada English first French first Option to display the non-official languages Spanish or Portuguese Neither Spanish Portuguese Display definitions, contexts, etc.


In which subject field? Skip to navigation Personal tools Log in.


HuR binding to the alternative 3′-terminal exon in the pre-messenger RNA promotes its splicing, and is reduced by topoisomerase inhibitors.

Metrics Show article metrics. These findings provide new insights into the evolution, function andmolecular regulation of alternative 3′-terminal exons. Alternative 3′-terminal exons, which use intronic polyadenylation sites, are generally less conserved episage expressed at lower levels than the last exon of genes. It is a method of producing structurally and functionally distinct proteins from the same gene and a method of developmental regulation.

This regulation is under control of the spliceosome and several splicing factors are also required to modulate the alternative usage of splice sites. Here we discover a class of human genes, in which the last exon appeared recently during evolution, and the major gene product uses epkssage alternative 3′-terminal exon corresponding to the ancestral last exon of the gene. Although many alterations are caused by mutations in splicing sequence i.