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Deceleration and acceleration in the rate of posterior neuropore closure during neurulation in the curly tail (ct) mouse embryo.

作者信息

van Straaten H W, Hekking J W, Copp A J, Bernfield M

机构信息

Department of Anatomy and Embryology, National University of Limburg, Maastricht, The Netherlands.

出版信息

Anat Embryol (Berl). 1992;185(2):169-74. doi: 10.1007/BF00185918.

DOI:10.1007/BF00185918
PMID:1536449
Abstract

Curly tail (ct) is a mouse mutant producing spinal neural tube defects as a result of delayed closure of the posterior neuropore (PNP). The purpose of the present study was to determine in ct/ct embryos the time of onset of the delay in PNP closure, and the pattern of this closure, as well as to study the possibility that reopening of the neural tube occurs. Normal spinal neurulation was studied in non-mutant Swiss (Sw) embryos. In the latter, the average PNP length diminished steadily between the 7- and 25-somite stages, and then decreased more rapidly, indicating an acceleration of closure rate, until the 30- to 32-somite stage, when all PNPs closed. PNP width decreased steadily between the stages of 7 and 30 somites. In ct/ct embryos the average PNP length showed a slight increase between the stage of 23 to 28 somites, indicating a temporary deceleration of closure rate, and the range of PNP sizes increased markedly. This was followed by a decrease in PNP length until the 37-somite stage, indicating an acceleration of closure rate. From the stage of 32 somites onwards, the proportion of embryos with closed PNPs gradually increased to 90%. The population of ct/ct embryos was subdivided. Embryos with large PNPs showed a marked deceleration of closure rate during a period of 11 somite stages, followed by a brief but very high acceleration of closure rate.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

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本文引用的文献

1
Abnormal neural fold development in trisomy 12 and trisomy 14 mouse embryos. I. Scanning electron microscopy.
J Embryol Exp Morphol. 1981 Dec;66:141-58.
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J Embryol Exp Morphol. 1982 Jun;69:151-67.
3
The curly-tail mouse: an experimental model for human neural tube defects.卷尾小鼠:一种人类神经管缺陷的实验模型。
Dis Model Mech. 2023 Mar 1;16(3). doi: 10.1242/dmm.049858. Epub 2023 Mar 14.
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Biomechanical coupling facilitates spinal neural tube closure in mouse embryos.生物力学偶联促进了小鼠胚胎脊髓神经管的闭合。
Proc Natl Acad Sci U S A. 2017 Jun 27;114(26):E5177-E5186. doi: 10.1073/pnas.1700934114. Epub 2017 Jun 12.
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Effects of the curly tail genotype on neuroepithelial integrity and cell proliferation during late stages of primary neurulation.卷尾基因型对原肠胚形成后期神经上皮完整性和细胞增殖的影响。
J Anat. 2001 Dec;199(Pt 6):645-55. doi: 10.1046/j.1469-7580.2001.19960645.x.
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Relationship between altered axial curvature and neural tube closure in normal and mutant (curly tail) mouse embryos.正常和突变(卷尾)小鼠胚胎中轴曲率改变与神经管闭合之间的关系。
Anat Embryol (Berl). 1996 Feb;193(2):123-30. doi: 10.1007/BF00214703.
10
Haplotype analysis of intra-specific backcross curly-tail mice confirms the localization of ct to chromosome 4.种内回交卷尾小鼠的单倍型分析证实了ct基因定位于4号染色体。
Mamm Genome. 1995 Apr;6(4):269-72. doi: 10.1007/BF00352414.
Life Sci. 1981 Oct 19;29(16):1607-15. doi: 10.1016/0024-3205(81)90061-8.
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