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Chimera Genetics: Understanding Hybrid Organisms

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What Are Chimeras? Genetic Mechanisms, Identification & Implications

Chimera Genetics: A genetic chimerism, also known as a chimaera, is a single organism made up of cells with several genotypes. In animals, it refers to an entity originating through two or even more zygotes, that may include blood cells with various blood types, slight differences in shape (phenotype), as well as the possession of both males and females sex organs unless the zygotes would be of opposite genders.

Animal chimaeras are created when several fertilised eggs are combined. The different types of tissue throughout plant chimaeras, on the other hand, may come from the very same zygote, and the distinction is sometimes owing to mutation while natural cell division. Genetic chimerism is usually undetectable on a casual examination, nevertheless, it's been discovered during the process of proving parentage.

Organ transplantation, which gives one particular tissue that originated from a separate genome, seems to be another aspect that chimerism can happen in animals. Bone marrow transplantation, for instance, also decides the recipient's blood type.


Animal Chimera

An animal chimera genetic engineering is a single organism made up of two or even more genetically different populations of cells originating from various zygotes engaging in sexual reproduction. The organism is termed a mosaic unless the various cells all come from that very same zygote. At least four parent cells are necessary to produce innate chimaeras (two fertilised eggs or early embryos tend to fuse together). Each population of cells retains its own personality, leading to an organism that is a combination of tissues. Human chimerism has indeed been documented in the past.

This disease may be innate or synthetic, resulting from the infusion of allogeneic hematopoietic cells throughout transplantation or transfusion, for instance.

Tetragametic Chimerism: Congenital chimerism is a form of tetragametic chimerism. The fertilisation of two different ova through two sperm, accompanied by aggregation of both the two at the blastocyst or zygote levels, causes this disease. This results in the formation of an organism with mixed cell lines. To put it differently, a chimaera is created by the union of two nonidentical twins. As a result, they may be either male or female, or who have mixed intersex traits. 

As the organism matures, it can acquire organs with different sets of chromosomes. The "chimera genetics may, for instance, do have liver made up of cells with a single set of chromosomes and a kidney made up of cells with a different set of chromosomes. It has happened in humans before, and it was once considered to be exceedingly rare, but new research shows that it is no longer the scenario.

Microchimerism: The existence of a limited number of cells that are genetically different from that of the host person is known as microchimerism. Many other people are born with several cells that are genetically similar to their mothers', and then as people grow older, the percentage of such cells decreases. People with more genetically similar cells to the mothers were shown to have increased rates of autoimmune disorders, possibly because the immune system is capable of killing these cells, and perhaps a common immune deficiency prohibits it from doing so, causing autoimmune issues.

Symbiotic Chimerism in Anglerfish: Genetic chimerism is a common occurrence in adult Ceratioid anglerfish which is a crucial component of their lifespan. When a male reaches maturity, he starts looking for a girl. The male anglerfish looks for a female anglerfish via powerful olfactory (or smell) receptors. The man, which is less than an inch long, cuts on her skin and produces an enzyme that helps to digest both his mouth as well as her body's skin, fusing the two at a time to the blood vessel point. Although the male's survival depends on this connection, this will ultimately consume him as the two anglerfish merge into a single hermaphroditic entity.

Germline Chimera in Genetic Engineering: Germline chimera in genetic engineering happens whenever an organism's germ cells (such as sperm cells and egg cells) are genetically different from its own. Due to placental fusion during development, marmosets can bear the reproductive cells of their (fraternal) twin siblings, according to new research. (Fraternal twins are almost always born to marmosets.)


Genetic Chimerism Human

Genetic chimera human have been observed in humans on a variety of occasions.

  • After refusing a mandatory sex examination in July 1950, Dutch sprinter Foekje Dillema has been expelled from the national team; subsequent inquiries found a Y-chromosome in her body cells, and research revealed that she was most definitely a 46,XX/46,XY mosaic female.

  • The British Medical Journal published a paper on a human chimaera in 1953. A woman's blood was discovered to contain two distinct blood groups. This is thought to be the product of her twin brother's cells residing in her body. According to a 1996 review, blood group chimerism is not uncommon.

  • In 1998, another human chimaera was identified, this time involving a male human with partially formed female organs due to chimerism. In-vitro fertilisation had been used to conceive him.

  • Lydia Fairchild has been refused public assistance in Washington state in the year 2002 after human chimera DNA" evidence suggested she is not really the mother of her son. The defence was able to prove that Fairchild, too, was a chimaera with two sets of DNA and that one of those sets may have been the mother of the twins, thanks to a prosecutor who learned of a human chimaera in New England named Karen Keegan.

  • In a 2002 article published in the New England Journal of Medicine, a woman was diagnosed with tetragametic chimerism upon undergoing kidney transplant preparations which needed the patient and her close family to conduct histocompatibility testing, which revealed that she's not the biological mother of two of the three children.

Chimera Identification

Chimerism is extremely rare, with just 100 reported cases in humans. Nevertheless, this could be because humans aren't conscious that they have this disease in the first place. Besides just some physical manifestations like hyper-pigmentation, hypo-pigmentation, or seeing two distinctly coloured eyes, chimerism typically seems to have no signs or symptoms. Such signs, furthermore, do not always indicate that an individual is a chimaera and can only be considered symptoms. The whole condition is normally discovered by mistake as a result of a forensic examination or curiosity about a negative maternity/paternity DNA test.

The identification of the previously unknown second genome is produced by simply undertaking a DNA test, that typically consists of either a quick cheek swab or a blood test, thus recognizing the person as a chimaera.

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FAQs on Chimera Genetics: Understanding Hybrid Organisms

1. What is a chimera in the context of genetics?

A genetic chimera is a single organism composed of cells with at least two different genotypes, originating from more than one zygote. This means the organism's body is a mosaic of genetically distinct cell lines. For example, this can occur naturally through the fusion of two separate embryos in the womb or can be created artificially for research purposes.

2. How is a chimera different from a hybrid, like a mule?

The difference lies in their genetic origins and cellular composition.

  • A hybrid, such as a mule, is formed from a single fertilisation event between the gametes (sperm and egg) of two different species. Every cell in the hybrid's body contains the same, uniform blend of chromosomes from both parent species.
  • A chimera is formed from the merging of two or more separate zygotes. This results in an organism containing distinct populations of cells, each with its own complete and different genetic makeup. A chimera has multiple sets of DNA coexisting in one body, while a hybrid has one single, blended set.

3. Can chimerism occur naturally in humans?

Yes, human chimerism can occur naturally, though it is considered rare. The most common mechanism is 'tetragametic chimerism,' where two fraternal (non-identical) twin embryos fuse in the womb during early development. The resulting single individual carries two distinct sets of DNA. This condition often goes completely undetected throughout a person's life and may only be discovered incidentally through medical or genetic testing.

4. What are some possible biological effects or signs of chimerism in an individual?

The effects of chimerism can be subtle or non-existent, but when present, they can manifest in various ways depending on which tissues contain the different cell lines. Potential signs include:

  • Patchy skin pigmentation: Lines or patches of slightly different skin tones.
  • Heterochromia: Having two different-coloured eyes if the cell lines controlling iris pigment are different.
  • Blood type discrepancies: An individual might show characteristics of two different blood types.
  • Intersex characteristics: This can occur if the fused embryos were of different sexes (e.g., one 46,XX and one 46,XY), potentially affecting the development of reproductive organs.

5. How does genetic mosaicism differ from chimerism?

Both chimerism and mosaicism describe an organism with genetically different cell populations, but their origins are distinct.

  • Chimerism originates from the fusion of two or more separate zygotes. It involves distinct cell populations from what would have been separate individuals.
  • Mosaicism originates from a single zygote. A genetic mutation or chromosomal event occurs during mitotic cell division after fertilisation. This creates a subset of cells that are genetically different from the original cells, but all cells trace back to the same initial zygote.

6. What is the scientific importance of creating chimeras in a laboratory?

Creating chimeras in a laboratory is a crucial tool in biomedical research. Its primary importance includes:

  • Studying Development: Scientists can track how specific cells differentiate into various tissues and organs, providing insights into embryology.
  • Disease Modelling: By introducing human cells with genetic diseases into an animal model, researchers can study the disease's progression and test potential therapies more effectively.
  • Organ Generation (Xenotransplantation): A major long-term goal is to grow human organs (like kidneys or hearts) in animals, such as pigs, for transplantation to address the shortage of donor organs.

7. Does having both XX and XY cell lines mean a chimera will be a hermaphrodite?

Not necessarily. While a 46,XX/46,XY chimera has the potential to develop both ovarian and testicular tissues (true hermaphroditism) or ambiguous genitalia, this is not a guaranteed outcome. The final physical phenotype depends heavily on the ratio and distribution of the XX and XY cells within the developing gonads and other reproductive structures. Many such chimeras develop a normal-appearing male or female phenotype and may be unaware of their sex-discordant genetic makeup.


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