李默怡

发布者:吴晓纯发布时间:2020-09-08浏览次数:9275

   


 


李默怡     副教授、博士生导师                  

 电  话

 Email: limoyi@seu.edu.cn

办公地点

江北校区汇川楼A405




个人简介:

19969月 — 20006月    学士, 微生物专业,华中农业大学

20009月 — 20036月    硕士, 生化工程专业,华中科技大学

20038月 — 20085月    博士, 植物病理专业,佛罗里达大学

20091月 — 20137月    博士后,佛罗里达大学

20141月 — 20162月    博士后,东南大学生命科学与技术学院

20162月至今               副研究员,东南大学生命科学与技术学院


研究方向:

1. 神经发育与退行性疾病的分子机理

2. 社交障碍及本能行为相关环路的调控机制



近期代表性论文:

* co-first author; # corresponding author

1. Peng S, Yang X, Meng S, Liu F, Lv Y, Yang H, Kong Y, Xie W, Li M#. Dual circuits originating from the ventral hippocampus independently facilitate affective empathy. Cell Rep. 2024 May 27;43(6):114277. doi: 10.1016/j.celrep.2024.114277. Epub ahead of print. PMID: 38805397.

2. Sun Y, Li M#, Geng J, Meng S, Tu R, Zhuang Y, Sun M, Rui M, Ou M, Xing G, Johnson TK, Xie W#. Neuroligin 2 governs synaptic morphology and function through RACK1-cofilin signaling in Drosophila. Commun Biol. 2023 Oct 18;6(1):1056. doi: 10.1038/s42003-023-05428-3.

3. Peng S, Gu W, Zhu W, Zhuang Y, Yang X, Lv Y, Meng S, Xie W, Li M#. A new AAV tool for highly preferentially targeting hippocampal CA2. (2023) Mol Brain. Jun 11;16(1):50. doi: 10.1186/s13041-023-01038-6.

4. Li M*#, Zhuang Y*, Batra R, Thomas JD, Li M, Nutter CA, Scotti MM, Carter HA, Wang ZJ, Huang XS, Pu CQ, Swanson MS, Xie W#. HNRNPA1-induced spliceopathy in a transgenic mouse model of myotonic dystrophy. (2020) Proc. Natl. Acad. Sci. U.S.A. 117(10):5472-5477.

5. Xing G*, Li M*, Sun Y, Rui M, Zhuang Y, Lv H, Han J, Jia Z, Xie W.  Neurexin-Neuroligin 1 regulates synaptic morphology and function via the WAVE regulatory complex in Drosophila neuromuscular junction. (2018) eLife;7: e30457

6. Batra R, Charizanis K, Manchanda M, Mohan A, Li M, Finn D J, Goodwin M, Zhang C, Sobczak K, Thornton C A., and Swanson MS. Loss of MBNL Leads to Disruption of Developmentally Regulated Alternative Polyadenylation in RNA Mediated Disease. (2014) Mol. Cell. 56: 311-322

7. Lee KY*, Li M*, Manchanda M, Batra R, Charizanis K, Mohan A, Warren SA, Finn D, Hong H, Ashraf H, Kasahara H, Chamberlain CM, Ranum LPW and Swanson MS. Compound loss of muscleblind-like function in myotonic dystrophy. (2013) EMBO Mol. Med. 5:1887-1900

8. Li M., Liang X., and Rollins J.A. Sclerotinia sclerotiorum gamma-glutamyl transpeptidase (Ss-Ggt1) is required for regulating glutathione accumulation and proper development of sclerotia and compound appressoria. (2012) Mol. Plant Microbe In. 25: 412-420

9. Li M. and Rollins J.A. The development-specific ssp1 and ssp2 genes of Sclerotinia sclerotiorum encode lectins with distinct yet compensatory regulation. (2010) Fungal Genet. Biol. 47: 531-538

10. Li M. and Rollins J.A. The development-specific protein (Ssp1) from Sclerotinia sclerotiorum is encoded by a novel gene expressed exclusively in sclerotium tissues. (2009) Mycologia. 101: 34-43