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本文引用的文献

1
Early lineage segregation between epiblast and primitive endoderm in mouse blastocysts through the Grb2-MAPK pathway.通过Grb2-MAPK途径在小鼠囊胚的外胚层和原始内胚层之间进行早期谱系分离。
Dev Cell. 2006 May;10(5):615-24. doi: 10.1016/j.devcel.2006.02.020.
2
Interaction between Oct3/4 and Cdx2 determines trophectoderm differentiation.Oct3/4与Cdx2之间的相互作用决定滋养外胚层分化。
Cell. 2005 Dec 2;123(5):917-29. doi: 10.1016/j.cell.2005.08.040.
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Mouse trophoblast stem cells.小鼠滋养层干细胞。
Methods Mol Med. 2006;121:125-48. doi: 10.1385/1-59259-983-4:123.
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Core transcriptional regulatory circuitry in human embryonic stem cells.人类胚胎干细胞中的核心转录调控回路。
Cell. 2005 Sep 23;122(6):947-56. doi: 10.1016/j.cell.2005.08.020.
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Cdx2 is required for correct cell fate specification and differentiation of trophectoderm in the mouse blastocyst.Cdx2对于小鼠囊胚中滋养外胚层正确的细胞命运特化和分化是必需的。
Development. 2005 May;132(9):2093-102. doi: 10.1242/dev.01801. Epub 2005 Mar 23.
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Imprinted X-inactivation in extra-embryonic endoderm cell lines from mouse blastocysts.小鼠囊胚中胚外内胚层细胞系的印记X染色体失活
Development. 2005 Apr;132(7):1649-61. doi: 10.1242/dev.01715.
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Spalt transcription factors are required for R3/R4 specification and establishment of planar cell polarity in the Drosophila eye.在果蝇眼睛中,Spalt转录因子是R3/R4特化和平面细胞极性建立所必需的。
Development. 2004 Nov;131(22):5695-702. doi: 10.1242/dev.01443.
8
Emerging asymmetry and embryonic patterning in early mouse development.小鼠早期发育过程中出现的不对称性与胚胎模式形成
Dev Cell. 2004 Aug;7(2):155-64. doi: 10.1016/j.devcel.2004.07.012.
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Lineage allocation and cell polarity during mouse embryogenesis.小鼠胚胎发育过程中的谱系分配和细胞极性
Semin Cell Dev Biol. 2004 Oct;15(5):583-97. doi: 10.1016/j.semcdb.2004.04.002.
10
Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation.转录组特征分析阐明了控制人类胚胎干细胞生长和分化的信号网络。
Nat Biotechnol. 2004 Jun;22(6):707-16. doi: 10.1038/nbt971. Epub 2004 May 16.

源自小鼠内细胞团的谱系依赖于Sall4的功能。

Murine inner cell mass-derived lineages depend on Sall4 function.

作者信息

Elling Ulrich, Klasen Christian, Eisenberger Tobias, Anlag Katrin, Treier Mathias

机构信息

Developmental Biology Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany.

出版信息

Proc Natl Acad Sci U S A. 2006 Oct 31;103(44):16319-24. doi: 10.1073/pnas.0607884103. Epub 2006 Oct 23.

DOI:10.1073/pnas.0607884103
PMID:17060609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1637580/
Abstract

Sall4 is a mammalian Spalt transcription factor expressed by cells of the early embryo and germ cells, an expression pattern similar to that of both Oct4 and Sox2, which play essential roles during early murine development. We show that the activity of Sall4 is cell-autonomously required for the development of the epiblast and primitive endoderm from the inner cell mass. Furthermore, no embryonic or extraembryonic endoderm stem cell lines could be established from Sall4-deficient blastocysts. In contrast, neither the development of the trophoblast lineage nor the ability to generate trophoblast cell lines from murine blastocysts was impaired in the absence of Sall4. These data establish Sall4 as an essential transcription factor required for the early development of inner cell mass-derived cell lineages.

摘要

Sall4是一种哺乳动物的Spalt转录因子,由早期胚胎细胞和生殖细胞表达,其表达模式与Oct4和Sox2相似,它们在小鼠早期发育过程中发挥着重要作用。我们发现,从内细胞团发育形成上胚层和原始内胚层,Sall4的活性是细胞自主所需的。此外,无法从Sall4缺陷型囊胚中建立胚胎或胚外内胚层干细胞系。相比之下,在没有Sall4的情况下,滋养层谱系的发育以及从小鼠囊胚中产生滋养层细胞系的能力均未受损。这些数据表明,Sall4是内细胞团来源的细胞谱系早期发育所需的一种重要转录因子。