与刺相关的突变会导致带有或没有遗传基因突变的骨形
Shoko Onodera1, Toshifumi Azuma1,2
1Department of Biochemistry, Tokyo Dental College, 2-9-18 Kanda Misaki-cho, Chiyoda-ku, Tokyo 101-0061, Japan.
International journal of molecular sciences
|August 26, 2023
概括
戈林综合征是一种影响骨并导致瘤的疾病,源自刺 (Hh) 信号通路的突变. 这篇评论探讨了Hh通路遗传学,戈林综合征和先进的诊断方法.
科学领域:
- 发展生物学 发展生物学
- 遗传学 遗传学 是一个
- 在瘤学瘤学.
背景情况:
- 刺 (Hh) 信号通路对于发育,骨形成和预防瘤至关重要.
- 戈林综合征,以骨异常和瘤倾向为特征,由Hh通路过度激活引起.
- 了解Hh通路遗传学对于诊断和管理相关疾病至关重要.
研究的目的:
- 审查戈林综合征中的表型和基因型-表型相关性,重点关注骨和面组织.
- 讨论Hh信号在骨发育和瘤发生中的作用.
- 为了突出 Hh 相关遗传疾病的诊断方法的进步.
主要方法:
- 关于戈林综合征,Hh通路遗传学和相关骨疾病的文献综述.
- 对受影响个体的基因型-表型关系的分析.
- 讨论下一代测序和基因面板在诊断中的应用.
主要成果:
- 戈林综合征与Hh通路基因的特定突变有关,影响骨和面发育.
- Hh通路的失调有助于发育异常和癌症.
- 下一代测序为与Hh相关的疾病提供了更好的诊断准确性.
结论:
- 信号是骨发育和瘤抑制的关键调节者.
- 基因分析,特别是使用先进的测序技术,对于诊断戈林综合征和相关疾病至关重要.
- 对Hh通路遗传学的进一步研究可以阐明骨疾病和癌症的机制.
更多相关视频
08:22A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
Published on: December 1, 2017
8.7K
07:26Quantitative PCR-based Assay to Measure Sonic Hedgehog Signaling in Cellular Model of Ciliogenesis
Published on: January 31, 2025
607
相关概念视频
Hedgehog Signaling Pathway
7.4K
The Hedgehog gene (Hh) was first discovered due to its control of the growth of disorganized, hair-like bristles phenotype in Drosophila, much like hedgehog spines. Hh plays a crucial role in the development of organs and the maintenance of homeostasis in both invertebrates and vertebrates. However, while Drosophila has only one Hh protein, mammals have multiple functional Hedgehog proteins - Sonic (Shh), Desert (Dhh), and Indian Hedgehog (Ihh). All of these homologous proteins have adapted to...
7.4K
Lethal Alleles
15.6K
Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
15.6K
Pleiotropy
40.6K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
40.6K
Mutations
83.6K
Overview
83.6K
The Retinoblastoma Gene
4.1K
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
4.1K
Genomic Imprinting and Inheritance
34.7K
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
34.7K
