文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

基于坐标外推系统(zFACE)的面部分析,用于发育中的斑马鱼的形态表型分析。

Facial analytics based on a coordinate extrapolation system (zFACE) for morphometric phenotyping of developing zebrafish.

机构信息

Pediatric Research Center, Department of Pediatrics, McGovern Medical School University of Texas Health Science Center-Houston, Houston, TX 77030, USA.

Genetics and Epigenetics Graduate Program, The University of Texas MD Anderson Cancer Center UTHealth Houston Graduate School of Biomedical Sciences, Houston, TX 77030, USA.

出版信息

Dis Model Mech. 2023 Jun 1;16(6). doi: 10.1242/dmm.049868. Epub 2023 Jun 2.


DOI:10.1242/dmm.049868
PMID:37102214
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10245138/
Abstract

Facial development requires a complex and coordinated series of cellular events that, when perturbed, can lead to structural birth defects. A quantitative approach to quickly assess morphological changes could address how genetic or environmental inputs lead to differences in facial shape and promote malformations. Here, we report on a method to rapidly analyze craniofacial development in zebrafish embryos using facial analytics based on a coordinate extrapolation system, termed zFACE. Confocal images capture facial structures and morphometric data are quantified based on anatomical landmarks present during development. The quantitative morphometric data can detect phenotypic variation and inform on changes in facial morphology. We applied this approach to show that loss of smarca4a in developing zebrafish leads to craniofacial anomalies, microcephaly and alterations in brain morphology. These changes are characteristic of Coffin-Siris syndrome, a rare human genetic disorder associated with mutations in SMARCA4. Multivariate analysis of zFACE data facilitated the classification of smarca4a mutants based on changes in specific phenotypic characteristics. Together, zFACE provides a way to rapidly and quantitatively assess the impact of genetic alterations on craniofacial development in zebrafish.

摘要

面部发育需要一系列复杂而协调的细胞事件,如果这些事件受到干扰,可能会导致结构出生缺陷。一种快速评估形态变化的定量方法可以研究遗传或环境因素如何导致面部形状的差异,并促进畸形的发生。在这里,我们报告了一种使用基于坐标外推系统的面部分析方法来快速分析斑马鱼胚胎颅面发育的方法,称为 zFACE。共聚焦图像捕获面部结构,基于发育过程中存在的解剖学标志来量化形态计量数据。定量形态计量数据可以检测表型变异,并提示面部形态的变化。我们应用这种方法表明,斑马鱼中 smarca4a 的缺失会导致颅面异常、小头畸形和大脑形态改变。这些变化是 Coffin-Siris 综合征的特征,这是一种罕见的人类遗传疾病,与 SMARCA4 基因突变有关。zFACE 数据的多变量分析有助于根据特定表型特征的变化对 smarca4a 突变体进行分类。总之,zFACE 提供了一种快速定量评估遗传改变对斑马鱼颅面发育影响的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a3/10245138/200fcb3f6e93/dmm-16-049868-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a3/10245138/b1d1dcb27a3f/dmm-16-049868-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a3/10245138/c0ef3b2447b2/dmm-16-049868-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a3/10245138/87011b5cd7a2/dmm-16-049868-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a3/10245138/0cbe5d8c09be/dmm-16-049868-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a3/10245138/200fcb3f6e93/dmm-16-049868-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a3/10245138/b1d1dcb27a3f/dmm-16-049868-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a3/10245138/c0ef3b2447b2/dmm-16-049868-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a3/10245138/87011b5cd7a2/dmm-16-049868-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a3/10245138/0cbe5d8c09be/dmm-16-049868-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a3/10245138/200fcb3f6e93/dmm-16-049868-g5.jpg

相似文献

[1]
Facial analytics based on a coordinate extrapolation system (zFACE) for morphometric phenotyping of developing zebrafish.

Dis Model Mech. 2023-6-1

[2]
Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A.

Am J Med Genet C Semin Med Genet. 2014-9

[3]
The variability of SMARCA4-related Coffin-Siris syndrome: Do nonsense candidate variants add to milder phenotypes?

Am J Med Genet A. 2020-9

[4]
Coffin-Siris syndrome is a SWI/SNF complex disorder.

Clin Genet. 2014-6

[5]
Novel Variants of the SMARCA4 Gene Associated with Autistic Features Rather Than Typical Coffin-Siris Syndrome in Eight Chinese Pediatric Patients.

J Autism Dev Disord. 2022-11

[6]
SMARCA4 inactivating mutations cause concomitant Coffin-Siris syndrome, microphthalmia and small-cell carcinoma of the ovary hypercalcaemic type.

J Pathol. 2017-9

[7]
Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4.

Mol Genet Genomic Med. 2019-4-11

[8]
Multiple Developmental Defects in Mutant Zebrafish with Features of Coffin-Siris Syndrome.

Int J Biol Sci. 2020

[9]
Coffin-Siris syndrome in two chinese patients with novel pathogenic variants of ARID1A and SMARCA4.

Genes Genomics. 2022-9

[10]
Coffin-Siris syndrome: phenotypic evolution of a novel SMARCA4 mutation.

Am J Med Genet A. 2014-7

引用本文的文献

[1]
Disruption of causes craniofacial anomalies in developing zebrafish.

Front Cell Dev Biol. 2023-8-16

本文引用的文献

[1]
PRDM paralogs antagonistically balance Wnt/β-catenin activity during craniofacial chondrocyte differentiation.

Development. 2022-2-15

[2]
The Expanding Role of Geometric Morphometrics in Craniofacial Surgery.

J Craniofac Surg. 2021-5-1

[3]
Zebrafish models of fetal alcohol spectrum disorders.

Genesis. 2021-11

[4]
Programmed Cell Death Not as Sledgehammer but as Chisel: Apoptosis in Normal and Abnormal Craniofacial Patterning and Development.

Front Cell Dev Biol. 2021-10-8

[5]
: Implications of an Altered Chromatin-Remodeling Gene for Cancer Development and Therapy.

Mol Cancer Ther. 2021-12

[6]
Transgenic fluorescent zebrafish lines that have revolutionized biomedical research.

Lab Anim Res. 2021-9-8

[7]
The power of zebrafish models for understanding the co-occurrence of craniofacial and limb disorders.

Genesis. 2021-2

[8]
Cellular and developmental basis of orofacial clefts.

Birth Defects Res. 2020-11

[9]
The Laboratory Domestication of Zebrafish: From Diverse Populations to Inbred Substrains.

Mol Biol Evol. 2020-4-1

[10]
Cranial growth in isolated sagittal craniosynostosis compared with normal growth in the first 6 months of age.

J Anat. 2020-1

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

推荐工具

医学文档翻译智能文献检索