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2
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Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of mutations.通过全基因组分析突变,对非综合征型唇裂伴/不伴腭裂中涉及的非编码元件进行优先级排序。
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8
Myosin-X knockout is semi-lethal and demonstrates that myosin-X functions in neural tube closure, pigmentation, hyaloid vasculature regression, and filopodia formation.肌球蛋白-X 敲除是半致死的,并表明肌球蛋白-X 在神经管闭合、色素形成、玻璃体血管退化和丝状伪足形成中发挥作用。
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本文引用的文献

1
Contact inhibition of locomotion in vivo controls neural crest directional migration.体内运动接触抑制控制神经嵴定向迁移。
Nature. 2008 Dec 18;456(7224):957-61. doi: 10.1038/nature07441. Epub 2008 Dec 10.
2
Wnt11r is required for cranial neural crest migration.颅神经嵴迁移需要Wnt11r。
Dev Dyn. 2008 Nov;237(11):3404-9. doi: 10.1002/dvdy.21758.
3
Myosin-10 and actin filaments are essential for mitotic spindle function.肌球蛋白-10和肌动蛋白丝对有丝分裂纺锤体功能至关重要。
J Cell Biol. 2008 Jul 14;182(1):77-88. doi: 10.1083/jcb.200804062. Epub 2008 Jul 7.
4
A gene regulatory network orchestrates neural crest formation.一个基因调控网络协调神经嵴的形成。
Nat Rev Mol Cell Biol. 2008 Jul;9(7):557-68. doi: 10.1038/nrm2428. Epub 2008 Jun 4.
5
Divergent roles for Eph and ephrin in avian cranial neural crest.Eph和ephrin在鸟类颅神经嵴中的不同作用。
BMC Dev Biol. 2008 May 21;8:56. doi: 10.1186/1471-213X-8-56.
6
Filopodia: molecular architecture and cellular functions.丝状伪足:分子结构与细胞功能
Nat Rev Mol Cell Biol. 2008 Jun;9(6):446-54. doi: 10.1038/nrm2406. Epub 2008 May 9.
7
Directional migration of neural crest cells in vivo is regulated by Syndecan-4/Rac1 and non-canonical Wnt signaling/RhoA.体内神经嵴细胞的定向迁移受Syndecan-4/Rac1和非经典Wnt信号通路/RhoA调控。
Development. 2008 May;135(10):1771-80. doi: 10.1242/dev.017350. Epub 2008 Apr 9.
8
Sequential roles for myosin-X in BMP6-dependent filopodial extension, migration, and activation of BMP receptors.肌球蛋白-X在骨形态发生蛋白6(BMP6)依赖的丝状伪足延伸、迁移及BMP受体激活过程中的顺序作用
J Cell Biol. 2007 Dec 31;179(7):1569-82. doi: 10.1083/jcb.200704010. Epub 2007 Dec 24.
9
The motor activity of myosin-X promotes actin fiber convergence at the cell periphery to initiate filopodia formation.肌球蛋白-X的运动活性促进肌动蛋白纤维在细胞周边汇聚,从而启动丝状伪足的形成。
J Cell Biol. 2007 Oct 22;179(2):229-38. doi: 10.1083/jcb.200703178.
10
Neuropilin 2/semaphorin 3F signaling is essential for cranial neural crest migration and trigeminal ganglion condensation.神经纤毛蛋白2/信号素3F信号传导对于颅神经嵴迁移和三叉神经节凝聚至关重要。
Dev Neurobiol. 2007 Jan;67(1):47-56. doi: 10.1002/dneu.20326.

肌球蛋白-X对非洲爪蟾颅神经嵴细胞的迁移能力至关重要。

Myosin-X is critical for migratory ability of Xenopus cranial neural crest cells.

作者信息

Nie Shuyi, Kee Yun, Bronner-Fraser Marianne

机构信息

Division of Biology 139-74, California Institute of Technology, Pasadena, CA 91125, USA.

出版信息

Dev Biol. 2009 Nov 1;335(1):132-42. doi: 10.1016/j.ydbio.2009.08.018. Epub 2009 Aug 25.

DOI:10.1016/j.ydbio.2009.08.018
PMID:19712673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3991693/
Abstract

The neural crest is a highly migratory cell population, unique to vertebrates, that forms much of the craniofacial skeleton and peripheral nervous system. In exploring the cell biological basis underlying this behavior, we have identified an unconventional myosin, myosin-X (Myo10) that is required for neural crest migration. Myo10 is highly expressed in both premigratory and migrating cranial neural crest (CNC) cells in Xenopus embryos. Disrupting Myo10 expression using antisense morpholino oligonucleotides leads to impaired neural crest migration and subsequent cartilage formation, but only a slight delay in induction. In vivo grafting experiments reveal that Myo10-depleted CNC cells migrate a shorter distance and fail to segregate into distinct migratory streams. Finally, in vitro cultures and cell dissociation-reaggregation assays suggest that Myo10 may be critical for cell protrusion and cell-cell adhesion. These results demonstrate an essential role for Myo10 in normal cranial neural crest migration and suggest a link to cell-cell interactions and formation of processes.

摘要

神经嵴是脊椎动物特有的高度迁移性细胞群体,它构成了大部分颅面骨骼和外周神经系统。在探索这种行为背后的细胞生物学基础时,我们鉴定出一种非常规肌球蛋白——肌球蛋白X(Myo10),它是神经嵴迁移所必需的。Myo10在非洲爪蟾胚胎的迁移前和迁移中的颅神经嵴(CNC)细胞中均高度表达。使用反义吗啉代寡核苷酸破坏Myo10的表达会导致神经嵴迁移受损以及随后的软骨形成,但诱导过程仅略有延迟。体内移植实验表明,Myo10缺失的CNC细胞迁移距离较短,且无法分离成不同的迁移流。最后,体外培养和细胞解离-重聚试验表明,Myo10可能对细胞突起和细胞间黏附至关重要。这些结果证明了Myo10在正常颅神经嵴迁移中的重要作用,并提示其与细胞间相互作用和突起形成有关。