The Role of G-Quadruplex RNA Motif in Fragile X Syndrome

Fragile X syndrome (FXS), the most common cause of inherited mental impairment, is caused by the loss of expression of the fragile X mental retardation protein (FMRP). As an RNA binding protein, FMRP has been proposed to regulate the transport and translation of specific message RNA (mRNA). It has been reported that FMRP uses its RGG box domain to bind mRNA targets that form a G-quadruplex structure, structure believed to be important for FMRP recognition of at least a subclass of its mRNA targets. We have hypothesized that the interaction of FMRP with selected relevant mRNA targets occurs in a G-quadruplex dependent manner. By analyzing the structure of two FMRP in vivo mRNA targets, Shank1 mRNA and BASP1 mRNA, and their interactions with FMRP, we showed a high-affinity interaction between Shank1 RNA G-quadruplex and FMRP. The other G-quadruplex forming mRNA BASP1, however, interacts with FMRP using other structural elements.

Name thesis:degree_name

MS

Level thesis:degree_level

Immediate Access

Discipline thesis:degree_discipline

Pharmaceutics

Year dc:date.available

2014

Author dc:creator

• Zhang, Yang

Contributors dc:contributor

• Mihaela-Rita Mihailescu
• James Drennen
• Wilson Meng

• FMRP
• Fragile X syndrome
• G-quadruplex
• RNA

Language dc:language

English

Repository record dc:identifier

https://dsc.duq.edu/etd/1411

OAI identifier oai:identifier

oai:dsc.duq.edu:etd-2427