The emerging physiological roles of the glycerophosphodiesterase family
Daniela Cordaa b, Maria Giovanna Moscaa b, Noriyasu Ohshimac d, Laura Grausoe f g h, Noriyuki Yanakai j k l m, Stefania Mariggiòa b✉
- aInstitute of Protein Biochemistry National Research Council Naples Italy
- bInstitute of Protein Biochemistry-National Research Council, Naples, Italy
- cDepartment of Biochemistry Gunma University Graduate School of Medicine Japan
- dDepartment of Biochemistry, Gunma University Graduate School of Medicine, Japan
- eInstitute of Biomolecular Chemistry National Research Council Naples Italy
- fInstitute of Biomolecular Chemistry
- gNational Research Council
- hNaples Italy
- iDepartment of Molecular and Applied Bioscience Graduate School of Biosphere Science Hiroshima University Japan
- jDepartment of Molecular and Applied Bioscience
- kGraduate School of Biosphere Science
- lHiroshima University
- mJapan
- ✉
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Abstract
The glycerophosphodiester phosphodiesterases are evolutionarily conserved proteins that have been linked to several patho/physiological functions, comprising bacterial pathogenicity and mammalian cell proliferation or differentiation. The bacterial enzymes do not show preferential substrate selectivities among the glycerophosphodiesters, and they are mainly dedicated to glycerophosphodiester hydrolysis, producing glycerophosphate and alcohols as the building blocks that are required for bacterial biosynthetic pathways. In some cases, this enzymatic activity has been demonstrated to contribute to bacterial pathogenicity, such as with Hemophilus influenzae. Mammalian glyerophosphodiesterases have high substrate specificities, even if the number of potential physiological substrates is continuously increasing. Some of these mammalian enzymes have been directly linked to cell differentiation, such as GDE2, which triggers motor neuron differentiation, and GDE3, the enzymatic activity of which is necessary and sufficient to induce osteoblast differentiation. Instead, GDE5 has been shown to inhibit skeletal muscle development independent of its enzymatic activity.

