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Updated: Aug 7, 2026

Detection of Alternative Splicing During Epithelial-Mesenchymal Transition
Published on: October 9, 2014
Characterization of novel splicing variants of the mouse MCF-2 (DBL) proto-oncogene
Koichiro Komai1, Naoko Mukae-Sakairi, Michinori Kitagawa
1Department of Rheumatology, Faculty of Health Sciences, School of Medicine, Kobe University, Kobe 654-0142, Japan.
Abstract:
MCF-2 (DBL) proto-oncogene is a prototype guanine nucleotide exchange factor (GEF) that modulates Rho GTPases such as Rho, Rac, and Cdc42. Although the partial sequence of mouse MCF-2 has been determined, its full-length cDNA and biochemical functions had not been elucidated. We isolated the complete mouse MCF-2 cDNA and obtained recombinant functional protein. Homology between the mouse and human MCF-2 (DBL) cDNAs is 75.08% identity and between the mouse and human amino acid sequences 74.52% identity. Analysis of tissue distribution showed that mouse MCF-2 mRNA is expressed in brain, kidney, intestine, and testis. The brain-specific transcript is an alternatively spliced derivative that omits the 48bp exon 11. A similar alternatively spliced mRNA product is also found in humans (DBL). Guanine nucleotide exchange activities of the testis-expressed mouse Mcf-2 and human Dbl were analyzed using RhoA, Rac1, and Cdc42 as substrates. RhoA and Cdc42 were activated similarly by both gene products, but Rac1 was activated only by the mouse product. The brain-specific Mcf-2 gene product, and its human counterpart, was less active than the respective testis-specific products. This indicates that the element encoded by the 48bp exon missing in the brain transcripts is necessary for full GEF activity. This report provides fundamental data on the structure of Mcf-2, which regulates a variety of cellular signaling pathways.
Insights
Mouse MCF-2 (DBL) proto-oncogene
Area of Science:
- Molecular Biology
- Cellular Signaling
- Oncogenes
Background:
- The MCF-2 (DBL) proto-oncogene is a key guanine nucleotide exchange factor (GEF) regulating Rho GTPases.
- Full-length cDNA and biochemical functions of mouse MCF-2 were previously uncharacterized.
Purpose of the Study:
- To isolate and characterize the full-length mouse MCF-2 cDNA and its recombinant functional protein.
- To compare mouse and human MCF-2 (DBL) sequence homology and biochemical activities.
Main Methods:
- Isolation of full-length mouse MCF-2 cDNA.
- Recombinant protein expression and purification.
- Guanine nucleotide exchange assays using RhoA, Rac1, and Cdc42 substrates.
- Analysis of tissue-specific mRNA expression and alternative splicing.
Main Results:
- Complete mouse MCF-2 cDNA isolated; 75.08% cDNA and 74.52% amino acid homology with human MCF-2.
- Mouse MCF-2 mRNA expressed in brain, kidney, intestine, and testis; brain transcript shows alternative splicing (exon 11 omission).
- Testis-expressed mouse Mcf-2 and human Dbl activated RhoA and Cdc42 similarly; only mouse Mcf-2 activated Rac1. Brain-specific products showed reduced GEF activity.
Conclusions:
- The 48bp exon 11 is crucial for full guanine nucleotide exchange factor activity.
- Alternative splicing in brain transcripts impacts MCF-2 GEF function.
- This study provides foundational data on MCF-2 structure and its role in cellular signaling pathways.
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