Chimera – Genetics
Chimera genetics includes various phenomena, from natural occurrences like symbiotic chimerism in anglerfish to artificial formation like germline chimeras in genetic engineering. Genetic chimerism in humans, including tetragametic and microchimerism, shows the complexity of genetic variation and its implications for health and identity. Identification of chimeras involves genetic testing of various tissues, diagnosing discrepancies in DNA profiles.
Chimera – Genetics
Chimera genetics refers to an organism containing cells with different genetic compositions. In genetics, human chimeras are individuals with cells from two or more genetically distinct sources. Identification of chimerism in humans involves genetic testing of multiple tissues or cells to detect variations in DNA profiles.
Chimerism can occur naturally through processes like twinning or fusion of embryos, and artificially through procedures like organ transplantation or gene therapy. Chimerism has applications in various fields like forensics, transplantation, and reproductive medicine. In this article, we will study the meaning of chimera, its formation, chimera in humans and its identification in detail.
Table of Content
- What is Chimera – Genetics?
- What Causes Chimerism?
- Symbiotic Chimerism in Anglerfish
- Animal Chimera
- Human Chimera
- Germline Chimera in Genetic Engineering
- Chimera Diagnosis
- Advantages of Chimera
- Disadvantages of Chimerism