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situs inversus突变体和野生型小鼠胚胎聚集嵌合体中手性不对称的发育

The development of handed asymmetry in aggregation chimeras of situs inversus mutant and wild-type mouse embryo.

作者信息

Brown N A, McCarthy A, Wolpert L

机构信息

MRC Experimental Embryology and Teratology Unit, Saint George's Hospital Medical School, London, UK.

出版信息

Development. 1990 Nov;110(3):949-54. doi: 10.1242/dev.110.3.949.

DOI:10.1242/dev.110.3.949
PMID:2088730
Abstract

Mutant iv/iv mice develop as if they have no sense of left and right, so the development of asymmetry is random: half normal, half as a mirror-image of normal, situs inversus. We have made aggregation chimeras of 8-cell stage iv/iv and +/+ embryos, transferred them into pseudopregnant mice, and examined their phenotype on day 10 of gestation. The contribution of mutant and wild-type cells to tissues of the embryo was estimated by strain-specific isozyme (GPI-1) analysis. We have also performed reciprocal embryo transfers, iv/iv blastocysts into +/+ mice, and vice versa. These transfers show that the development of handed asymmetry is determined by embryonic genotype, and is unaffected by the maternal environment (at least after day 3), or by the procedures of embryo collection, culture and transfer. Our observations on the development of 21 viable chimeric embryos show that neither iv/iv nor +/+ cells are dominant. All embryos (12) with less than 50% contribution of iv/iv cells to the heart developed with normal situs. Of 9 embryos with greater than 50% iv/iv cells, only 2 developed with inverted situs. These findings suggests that there was partial 'rescue' of embryos by some influence of normal over mutant cells. However, we cannot, statistically, exclude an alternative interpretation that cells are behaving autonomously. Interestingly, the embryos that developed with inverted situs were unique in having greater than two thirds contribution of iv/iv cells to both the heart and the visceral yolk-sac.

摘要

iv/iv突变小鼠的发育就好像它们没有左右之分,因此不对称发育是随机的:一半正常,一半是正常的镜像,即内脏反位。我们制作了8细胞期iv/iv胚胎和+/+胚胎的聚合嵌合体,将它们移植到假孕小鼠体内,并在妊娠第10天检查它们的表型。通过菌株特异性同工酶(GPI-1)分析估计突变细胞和野生型细胞对胚胎组织的贡献。我们还进行了 reciprocal embryo transfers,将iv/iv囊胚移植到+/+小鼠体内,反之亦然。这些移植表明,手性不对称的发育由胚胎基因型决定,不受母体环境(至少在第3天后)或胚胎采集、培养和移植程序的影响。我们对21个存活嵌合胚胎发育的观察表明,iv/iv细胞和+/+细胞都不占主导地位。所有iv/iv细胞对心脏的贡献小于50%的胚胎(12个)都正常发育。在9个iv/iv细胞贡献大于50%的胚胎中,只有2个内脏反位发育。这些发现表明,正常细胞对突变细胞的某种影响对胚胎有部分“挽救”作用。然而,从统计学角度,我们不能排除细胞自主行为的另一种解释。有趣的是,内脏反位发育的胚胎的独特之处在于,iv/iv细胞对心脏和内脏卵黄囊的贡献都超过三分之二。

相似文献

1
The development of handed asymmetry in aggregation chimeras of situs inversus mutant and wild-type mouse embryo. situs inversus突变体和野生型小鼠胚胎聚集嵌合体中手性不对称的发育
Development. 1990 Nov;110(3):949-54. doi: 10.1242/dev.110.3.949.
2
The development of asymmetry: the sidedness of drug-induced limb abnormalities is reversed in situs inversus mice.不对称性的发展:药物诱导的肢体异常的左右侧性在 situs inversus 小鼠中发生逆转。
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Situs inversus in the developing mouse: proteins affected by the iv mutation (genocopy) and the teratogen retinoic acid (phenocopy).发育中小鼠的内脏反位:受iv突变(基因拷贝)和致畸剂视黄酸(表型拷贝)影响的蛋白质。
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Germ cell nuclei of male fetal mice can support development of chimeras to midgestation following serial transplantation.雄性胎鼠的生殖细胞核在连续移植后能够支持嵌合体发育至妊娠中期。
Development. 1995 Mar;121(3):779-83. doi: 10.1242/dev.121.3.779.
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Conserved left-right asymmetry of nodal expression and alterations in murine situs inversus.节点表达的保守左右不对称性与小鼠内脏反位的改变。
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Duplication/deficiency mapping of situs inversus viscerum (iv), a gene that determines left-right asymmetry in the mouse.内脏反位(iv)基因的重复/缺失图谱分析,该基因决定小鼠的左右不对称性。
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