Suppr超能文献

在近交C57BL/6J遗传背景上的一个条件性平滑(smo)等位基因具有一个亚效性smo突变体表型。

A conditional smoothened (smo) allele on an inbred C57BL/6J genetic background has a hypomorphic smo mutant phenotype.

作者信息

Houghtaling Scott, Gombart Sean K, Ho Tzu-Hua, Huang Grace, Beier David R

机构信息

Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, USA.

Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, USA; Department of Pediatrics, Division of Genetic Medicine, University of Washington School of Medicine, Seattle, WA, USA.

出版信息

Dev Biol. 2025 Feb;518:71-76. doi: 10.1016/j.ydbio.2024.11.010. Epub 2024 Nov 26.

Abstract

We have introduced the floxed allele of Smoothened (Smo) carried by the mouse line Smo into the C57BL/6J strain by serial backcross. Recapitulation of the Smo null phenotype was confirmed by deleting the allele using E2a-cre and intercrossing heterozygous Smo ± mice. No homozygous mutant embryos were identified at E9.5, suggesting the null phenotype is at least as severe as that observed on a mixed genetic background. While healthy and fertile homozygous floxed mice were regularly obtained after intercrosses, their numbers at weaning were reduced relative to Mendelian expectation, suggesting the unrecombined allele is itself hypomorphic. This hypothesis is supported by characterization of transcription of the floxed allele, which revealed that its expression was variably reduced relative to wild-type Smo.

摘要

我们通过连续回交将携带Smo基因(Smo)的floxed等位基因从小鼠品系Smo引入到C57BL/6J品系中。通过使用E2a-cre删除等位基因并使杂合子Smo ± 小鼠杂交,证实了Smo基因敲除表型的重现。在E9.5时未鉴定出纯合突变胚胎,这表明该基因敲除表型至少与在混合遗传背景下观察到的一样严重。虽然在杂交后经常能获得健康且可育的纯合floxed小鼠,但它们断奶时的数量相对于孟德尔预期有所减少,这表明未重组的等位基因本身是亚效等位基因。这一假设得到了对floxed等位基因转录特征的支持,该特征表明其表达相对于野生型Smo有不同程度的降低。

相似文献

1
A conditional smoothened (smo) allele on an inbred C57BL/6J genetic background has a hypomorphic smo mutant phenotype.
Dev Biol. 2025 Feb;518:71-76. doi: 10.1016/j.ydbio.2024.11.010. Epub 2024 Nov 26.
2
A novel mouse Fgfr2 mutant, hobbyhorse (hob), exhibits complete XY gonadal sex reversal.
PLoS One. 2014 Jun 23;9(6):e100447. doi: 10.1371/journal.pone.0100447. eCollection 2014.
3
G-protein receptor kinases 2, 5 and 6 redundantly modulate Smoothened-GATA transcriptional crosstalk in fetal mouse hearts.
J Mol Cell Cardiol. 2018 Aug;121:60-68. doi: 10.1016/j.yjmcc.2018.06.009. Epub 2018 Jun 30.
5
Effect of the sonic hedgehog receptor smoothened on the survival and function of dopaminergic neurons.
Exp Neurol. 2016 Sep;283(Pt A):235-45. doi: 10.1016/j.expneurol.2016.06.013. Epub 2016 Jun 15.
6
Cholesterol Modification of Smoothened Is Required for Hedgehog Signaling.
Mol Cell. 2017 Apr 6;66(1):154-162.e10. doi: 10.1016/j.molcel.2017.02.015. Epub 2017 Mar 23.
7
Hypomorphic Smo mutant with inefficient ciliary enrichment disrupts the highest level of vertebrate Hedgehog response.
Dev Biol. 2018 May 15;437(2):152-162. doi: 10.1016/j.ydbio.2018.03.019. Epub 2018 Mar 20.
8
Recovery of taste organs and sensory function after severe loss from Hedgehog/Smoothened inhibition with cancer drug sonidegib.
Proc Natl Acad Sci U S A. 2017 Nov 28;114(48):E10369-E10378. doi: 10.1073/pnas.1712881114. Epub 2017 Nov 13.
9
Cholesterylation of Smoothened is a calcium-accelerated autoreaction involving an intramolecular ester intermediate.
Cell Res. 2022 Mar;32(3):288-301. doi: 10.1038/s41422-022-00622-0. Epub 2022 Feb 4.

引用本文的文献

本文引用的文献

1
Cellular and molecular mechanisms of Hedgehog signalling.
Nat Rev Mol Cell Biol. 2023 Sep;24(9):668-687. doi: 10.1038/s41580-023-00591-1. Epub 2023 Mar 17.
3
Content and Performance of the MiniMUGA Genotyping Array: A New Tool To Improve Rigor and Reproducibility in Mouse Research.
Genetics. 2020 Dec;216(4):905-930. doi: 10.1534/genetics.120.303596. Epub 2020 Oct 16.
4
Expanded encyclopaedias of DNA elements in the human and mouse genomes.
Nature. 2020 Jul;583(7818):699-710. doi: 10.1038/s41586-020-2493-4. Epub 2020 Jul 29.
5
Hypomorphic Smo mutant with inefficient ciliary enrichment disrupts the highest level of vertebrate Hedgehog response.
Dev Biol. 2018 May 15;437(2):152-162. doi: 10.1016/j.ydbio.2018.03.019. Epub 2018 Mar 20.
7
Transcriptome Analysis of Targeted Mouse Mutations Reveals the Topography of Local Changes in Gene Expression.
PLoS Genet. 2016 Feb 3;12(2):e1005691. doi: 10.1371/journal.pgen.1005691. eCollection 2016 Feb.
8
Downregulating hedgehog signaling reduces renal cystogenic potential of mouse models.
J Am Soc Nephrol. 2014 Oct;25(10):2201-12. doi: 10.1681/ASN.2013070735. Epub 2014 Apr 3.
9
Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity.
J Clin Invest. 2012 Nov;122(11):4257-73. doi: 10.1172/JCI64313. Epub 2012 Oct 15.
10
Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease.
Kidney Int. 2009 Apr;75(8):848-55. doi: 10.1038/ki.2008.686. Epub 2009 Jan 21.

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