Faculty Information |
|
Article types | Introduction |
Language | English |
Refereed paper | Not refereed |
Title | Stories of spinster with various faces: from courtship rejection to tumor metastasis rejection. |
Journal | Formal name:Journal of neurogenetics Abbreviation:J Neurogenet ISSN code:1563526001677063 |
Volume, Number, Page | pp.1-6 |
Papers・Author | Nakano Yoshiro |
Publication date | 2019/04 |
Papers・Description | The Drosophila spinster (spin) mutant was isolated as a mutant that showed abnormal morphology and function in the nervous system. The spin defect induces neural degeneration similar to human lysosomal storage diseases. Various studies have shown that Spin proteins are localized in lysosomes and participate in the late stages of the autophagic process. Vertebrates have three spinster orthologs, Spns1, Spns2, and Spns3. A defect in Spns1 caused a short lifespan with aberrant lysosomal function in zebrafish. Spns2 was originally isolated as the gene responsible for abnormal heart development and was identified as a sphingosine 1-phosphate transporter in zebrafish. An endothelial cell-specific defect in Spns2 resulted inimpaired egress of lymphocytes and the prevention of tumor metastasis in mice. Herein, I reviewed the history of spin/Spns research and discussed the conserved and newly diverged spin/Spns function and possible implications for human diseases. |
DOI | 10.1080/01677063.2019.1586897 |
PMID | 30939968 |