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Sample Preparation for Mass Spectrometry-based Identification of RNA-binding Regions
Published on: September 28, 2017
Identification and structural analysis of human RBM8A and RBM8B: two highly conserved RNA-binding motif proteins that
A M Salicioni1, M Xi, L A Vanderveer
1Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111, USA.
Abstract:
The OVCA1 gene is a candidate for the breast and ovarian tumor suppressor gene at chromosome 17p13.3. To help determine the function(s) of OVCA1, we used a yeast two-hybrid screening approach to identify OVCA1-associating proteins. One such protein, which we initially referred to as BOV-1 (binder of OVCA1-1) is 173 or 174 amino acids in length and appears to be a new member of a highly conserved RNA-binding motif (RBM) protein family that is highly conserved evolutionarily. Northern blot analysis revealed that BOV-1 is ubiquitously expressed and that three distinct messenger RNA species are expressed, 1-, 3.2-, and 5.8-kb transcripts. The 1-kb transcript is the most abundant and is expressed at high levels in the testis, heart, placenta, spleen, thymus, and lymphocytes. Using fluorescence in situ hybridization and the 5.8-kb complementary DNA probe, we determined that BOV-1 maps to both chromosome 5q13-q14 and chromosome 14q22-q23. Further sequence analysis determined that the gene coding the 1- and the 3.2-kb transcripts (HGMW-approved gene symbol RBM8A) maps to 14q22-q23, whereas a second highly related gene coding for the 5.8-kb transcript resides at chromosome 5q13-q14 (HGMW-approved gene symbol RBM8B). The predicted proteins encoded by RBM8A and RBM8B are identical except that RBM8B is 16 amino acids shorter at its N-terminus. Molecular modeling of the RNA-binding domain of RBM8A and RBM8B, based on homology to the sex-lethal protein of Drosophila, identifies conserved residues in the RBM8 protein family that are likely to contact RNA in a protein-RNA complex. The conservation of sequence and structure through such an evolutionarily divergent group of organisms suggests an important function for the RBM8 family of proteins.
Insights
Researchers identified a new RNA-binding motif (RBM) protein family member, BOV-1, that associates with OVCA1. This protein family, RBM8A and RBM8B, is highly conserved and likely plays a crucial role in protein-RNA interactions.
Area of Science:
- Molecular Biology
- Genetics
- Protein Interactions
Background:
- OVCA1 is a candidate tumor suppressor gene located at chromosome 17p13.3.
- Understanding OVCA1's function requires identifying its interacting proteins.
Purpose of the Study:
- To identify proteins that associate with OVCA1 using yeast two-hybrid screening.
- To characterize a novel OVCA1-associating protein, initially named BOV-1.
Main Methods:
- Yeast two-hybrid screening to identify protein interactions.
- Northern blot analysis to determine BOV-1 expression patterns.
- Fluorescence in situ hybridization (FISH) to map BOV-1 gene locations.
- Sequence analysis and molecular modeling to predict protein structure and function.
Main Results:
- A novel protein, BOV-1, was identified and characterized as a member of the RNA-binding motif (RBM) protein family.
- BOV-1 is ubiquitously expressed with three distinct mRNA transcripts (1-, 3.2-, and 5.8-kb).
- The gene for BOV-1, RBM8A, maps to chromosome 14q22-q23, while a related gene, RBM8B, maps to chromosome 5q13-q14.
- Molecular modeling suggests conserved residues in RBM8A and RBM8B are critical for RNA binding.
Conclusions:
- BOV-1 represents a new member of the evolutionarily conserved RBM8 protein family.
- The RBM8 family, including RBM8A and RBM8B, likely plays a significant role in protein-RNA interactions due to conserved structural elements.
- Further research into the RBM8 family is warranted to elucidate its specific biological functions.
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