相关实验视频
Updated: Jul 7, 2026

11:13
Using Mouse Oocytes to Assess Human Gene Function During Meiosis I
Published on: April 10, 2018
概括
BALB/c小鼠拥有两个具有相似结构的β-环球蛋白基因,包括中间DNA序列. 在编码区域之外存在有限的同质性,这可能解释了坐标基因表达.
科学领域:
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
背景情况:
- BALB/c小鼠有两个非类β-环球蛋白基因.
- 一个基因片段以前被克隆,发现它包含了中间的DNA序列.
研究的目的:
- 为了克隆和描述第二个含有β-环球蛋白基因的DNA片段.
- 为了比较两个β-环球蛋白基因的结构,以了解它们的坐标表达.
主要方法:
- 基因组DNA克隆和表征.
- 限制内核酶分析.
- 异重复结构可视化.异重复结构可视化.
主要成果:
- 第二个β-环球蛋白基因片段被克隆和表征.
- 这种基因也被中间的DNA序列中断,其位置与第一个基因相似.
- 在编码序列之外发现了有限的同质性 (几百个基对),主要是围绕着编码区域并邻中间序列.
结论:
- 在BALB/c小鼠中的两个β-环球蛋白基因具有结构上的相似性,包括中间序列.
- 在编码区域之外的有限序列同质性可能在它们的坐标表达和中间序列消除中发挥作用.
相关概念视频
Gene Families
Gene families consist of groups of genes proposed to have originated from a common ancestor. Typically these arise through events in which a gene or genes are mistakenly duplicated during cell division. Unlike their parent genes (which are subject to selection pressure to maintain function), these gene copies do not need to preserve their sequences and may evolve at a relatively faster rate.
Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...
Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...
Protein Families
Protein families are groups of homologous proteins; that is, they have similarities in amino acid sequences and three-dimensional structures. Protein families usually occur because of gene duplication, where an additional copy of a gene is inserted into the genome of an organism. Mutations that change the amino acids but still allow the protein to be properly synthesized, will lead to new protein family members. If these new proteins contain similar amino acids in key locations, protein...
Evolutionary Relationships through Genome Comparisons
Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
Multi-species Conserved Sequences
Next-generation sequencing technologies have created large genomic databases of a variety of animals and plants. Ever since the human genome project was completed, scientists studied the genome of primates, mammals, and other phylogenetically distant living beings. Such large-scale studies have provided new insights into the evolutionary relationship between organisms.
Although the genome of each species varies greatly from each other, a few sequences are highly conserved. Such conserved DNA...
Although the genome of each species varies greatly from each other, a few sequences are highly conserved. Such conserved DNA...
Gene Duplication and Divergence
The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was generated by gene duplication and divergence, indicating its critical role in evolution.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are characterized.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are characterized.
Comparing Copy Number Variations and SNPs
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...

