Suppr超能文献

18.5kDa 髓鞘碱性蛋白 SH3 配体脯氨酸取代和苏氨酸假磷酸化降低其与 Fyn-SH3 结构域的亲和力,并改变少突胶质细胞的突起发育和蛋白定位。

Proline substitutions and threonine pseudophosphorylation of the SH3 ligand of 18.5-kDa myelin basic protein decrease its affinity for the Fyn-SH3 domain and alter process development and protein localization in oligodendrocytes.

机构信息

Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.

出版信息

J Neurosci Res. 2012 Jan;90(1):28-47. doi: 10.1002/jnr.22733. Epub 2011 Sep 1.

Abstract

The developmentally regulated myelin basic proteins (MBPs), which arise from the golli (gene of oligodendrocyte lineage) complex, are highly positively charged, intrinsically disordered, multifunctional proteins having several alternatively spliced isoforms and posttranslational modifications, and they play key roles in myelin compaction. The classic 18.5-kDa MBP isoform has a proline-rich region comprising amino acids 92-99 (murine sequence -T(92)PRTPPPS(99)-) that contains a minimal SH3 ligand domain. We have previously shown that 18.5-kDa MBP binds to several SH3 domains, including that of Fyn, a member of the Src family of tyrosine kinases involved in a number of signaling pathways during CNS development. To determine the physiological role of this binding as well as the role of phosphorylation of Thr92 and Thr95, in the current study we have produced several MBP variants specifically targeting phosphorylation sites and key structural regions of MBP's SH3 ligand domain. Using isothermal titration calorimetry, we have demonstrated that, compared with the wild-type protein, these variants have lower affinity for the SH3 domain of Fyn. Moreover, overexpression of N-terminal-tagged GFP versions in immortalized oligodendroglial N19 and N20.1 cell cultures results in aberrant elongation of membrane processes and increased branching complexity and inhibits the ability of MBP to decrease Ca(2+) influx. Phosphorylation of Thr92 can also cause MBP to traffic to the nucleus, where it may participate in additional protein-protein interactions. Coexpression of MBP with a constitutively active form of Fyn kinase resulted in membrane process elaboration, a phenomenon that was abolished by point amino acid substitutions in MBP's SH3 ligand domain. These results suggest that MBP's SH3 ligand domain plays a key role in intracellular protein interactions in vivo and may be required for proper membrane elaboration of developing oligodendrocytes and, further, that phosphorylation of Thr92 and Thr95 can regulate this function.

摘要

发育调控髓鞘碱性蛋白(MBP)来自 golli(少突胶质细胞谱系基因)复合物,是高度带正电荷、无序的多功能蛋白,具有多个选择性剪接的异构体和翻译后修饰,在髓鞘紧缩中发挥关键作用。经典的 18.5kDa MBP 异构体具有脯氨酸丰富的区域,包含氨基酸 92-99(鼠序列-T(92)PRTPPPS(99)-),其中包含最小的 SH3 配体结构域。我们之前已经表明,18.5kDa MBP 与几个 SH3 结构域结合,包括 Fyn 的 SH3 结构域,Fyn 是参与中枢神经系统发育过程中许多信号通路的 Src 家族酪氨酸激酶的成员。为了确定这种结合的生理作用以及 Thr92 和 Thr95 磷酸化的作用,在当前研究中,我们专门针对 MBP 的 SH3 配体结构域的磷酸化位点和关键结构区域产生了几种 MBP 变体。使用等温滴定量热法,我们已经证明与野生型蛋白相比,这些变体与 Fyn 的 SH3 结构域的亲和力较低。此外,在永生化少突胶质细胞 N19 和 N20.1 细胞培养物中过表达 N 端标记的 GFP 变体导致膜过程的异常伸长和分支复杂性增加,并抑制 MBP 降低 Ca(2+)内流的能力。Thr92 的磷酸化也可以导致 MBP 向核内运输,在核内它可能参与其他蛋白质-蛋白质相互作用。MBP 与组成型激活形式的 Fyn 激酶共表达导致膜过程的细化,这一现象在 MBP 的 SH3 配体结构域中的点氨基酸取代被消除。这些结果表明,MBP 的 SH3 配体结构域在体内细胞内蛋白质相互作用中发挥关键作用,并且可能是发育中的少突胶质细胞正确的膜细化所必需的,并且 Thr92 和 Thr95 的磷酸化可以调节这种功能。

相似文献

引用本文的文献

6
Oligodendroglial membrane dynamics in relation to myelin biogenesis.少突胶质细胞膜动力学与髓鞘生物发生的关系
Cell Mol Life Sci. 2016 Sep;73(17):3291-310. doi: 10.1007/s00018-016-2228-8. Epub 2016 May 3.
7
Fyn in Neurodevelopment and Ischemic Brain Injury.Fyn在神经发育和缺血性脑损伤中的作用
Dev Neurosci. 2015;37(4-5):311-20. doi: 10.1159/000369995. Epub 2015 Feb 17.

本文引用的文献

7
Cells of the oligodendroglial lineage, myelination, and remyelination.少突胶质细胞谱系的细胞、髓鞘形成和髓鞘再生。
Biochim Biophys Acta. 2011 Feb;1812(2):184-93. doi: 10.1016/j.bbadis.2010.09.010. Epub 2010 Sep 29.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验