Related Experiment Video
Updated: Mar 18, 2026

11:34
Exploring Sequence Space to Identify Binding Sites for Regulatory RNA-Binding Proteins
Published on: August 9, 2019
7.2K
The bicoid mRNA localization factor Exuperantia is an RNA-binding pseudonuclease.
Daniela Lazzaretti1, Katharina Veith1, Katharina Kramer2,3
1Max Planck Institute for Developmental Biology, Tübingen, Germany.
Nature Structural & Molecular Biology
|July 5, 2016
Summary
Exuperantia (Exu) protein, crucial for bicoid mRNA localization in Drosophila, functions as a noncanonical RNA-binding protein. Its dimeric structure, not enzymatic activity, is essential for binding and localizing bicoid mRNA.
Area of Science:
- Developmental Biology
- Molecular Biology
- Structural Biology
Background:
- Anterior patterning in Drosophila is regulated by bicoid (bcd) mRNA localization.
- Exuperantia (Exu) is implicated in binding and localizing bcd mRNA.
Purpose of the Study:
- To elucidate the structural and functional mechanisms of Exuperantia (Exu) in bicoid mRNA localization.
- To determine how Exu's structure relates to its RNA-binding and localization functions.
Main Methods:
- X-ray crystallography to determine Exu structure.
- In vitro RNA binding assays.
- Structure-guided mutagenesis and functional assays in Drosophila.
Main Results:
- Exu forms a dimer through its EXO-like and SAM-like domains.
- Exu possesses a degenerate catalytic site but binds RNA directly via its EXO-like domain.
- The SAM-like domain is crucial for RNA binding, and Exu binds a specific structure in the bcd 3' UTR.
- Exu dimerization is essential for bcd mRNA localization.
Conclusions:
- Exuperantia is a noncanonical RNA-binding protein with a unique EXO-SAM domain architecture.
- Exu functions as a homodimer to bind and localize bicoid mRNA, independent of exonuclease activity.
- The study reveals a novel mechanism for mRNA localization in early development.
Related Concept Videos
Nonsense-mediated mRNA Decay
12.0K
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
12.0K
Nonsense-mediated mRNA Decay
3.6K
3.6K
Nuclear Export of mRNA
9.0K
Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...
9.0K
Nuclear Export of mRNA
5.6K
5.6K
Nuclear Export
5.1K
The nucleus restricts several proteins within and allows others to pass. The restricted proteins possess a nuclear retention sequence or NRS, anchoring them to the nuclear lamins and preventing their transport to the cytosol. The non-restricted proteins, after their synthesis, are transported to their site of action, such as the cytosol or other organelles, with the help of nuclear export signals or NES.
NES are of three types- the canonical 10-residue long leucine-rich signal and other...
NES are of three types- the canonical 10-residue long leucine-rich signal and other...
5.1K
Leaky Scanning
5.8K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA. Marilyn Kozak discovered that the sequence RCCAUGG (where R...
5.8K

