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Extranuclear inheritance

life science Maturity 11-13 Next article →

Most genetic information is stored within the cell nucleus. However, some genes exist outside of this central area. This process is known as extranuclear inheritance or cytoplasmic inheritance.

Mitochondrion structure
Mitochondrion structure

It involves the transmission of genes located in the cytoplasm. This occurs in most eukaryotes, which are complex organisms. These genes are often found within specialized structures called organelles. They can also be transmitted through cellular parasites like bacteria or viruses.

Organelles like mitochondria and chloroplasts play a vital role in cellular life. Mitochondria are responsible for transforming energy through a process called cellular respiration. Chloroplasts are found in plants and algae to produce sugars via photosynthesis. Both organelles contain their own unique DNA. This extranuclear DNA replicates independently of the DNA in the nucleus. While nuclear DNA replicates once before cell division, extranuclear DNA replicates in response to energy needs. This replication happens throughout the entire lifespan of a cell. Because they replicate separately, these genomes rarely undergo recombination. Recombination is the mixing of genes that is common in nuclear genomes.

There are three general types of extranuclear inheritance. The first is vegetative segregation. This occurs when organelles replicate and partition randomly during mitotic cell division. This results in daughter cells receiving a random sample of the parent's organelles. An example is seen in the mitochondria of asexually replicating yeast cells. The second type is uniparental inheritance. This occurs when only one parent contributes organellar DNA to the offspring.

Egg cell fertilization - Zygote
Egg cell fertilization - Zygote

The third type is biparental inheritance. This happens when both parents contribute organellar DNA. This is less common and usually only occurs in specific species. For instance, the yeast Saccharomyces cerevisiae shows biparental mitochondrial inheritance when two haploid cells fuse.

Uniparental inheritance is a very common way for these genes to move. In humans, mitochondrial inheritance is strictly maternal. The mother's mitochondria are passed to the offspring through the egg cell.

Egg cell fertilization - Zygote
Egg cell fertilization - Zygote

During fertilization, the head of the sperm typically enters the egg. The middle part of the sperm, which contains its mitochondria, is left behind. Consequently, the father's mitochondrial DNA is usually excluded from the zygote. This explains why mitochondrial diseases are inherited from the mother rather than the father. While very rare cases of paternal inheritance have been reported, they require more investigation.

Chloroplast inheritance can also be uniparental, but it is more complex. While often thought to be maternal, researchers have identified paternal inheritance in many species. In the tobacco plant, Nicotiana tabacum, the mode of inheritance can change. It can be maternal, paternal, or even biparental within the same species. The way chloroplasts are inherited in tobacco is affected by temperature. It is also influenced by the enzymatic activity of an exonuclease during male gametogenesis.

Extranuclear transmission can also involve parasites like viruses or bacteria. One specific example is perinatal transmission of viral genomes. This refers to the movement of material from a mother to a fetus. The perinatal period begins before birth and ends about one month after birth. During this time, viral material can be passed through the bloodstream or breastmilk. This is a major concern for mothers carrying viruses such as HIV or hepatitis C. Additionally, symbiotic bacteria in the cytoplasm can be inherited by insects and protists.

Scientists first established the basis for extranuclear inheritance by studying a fungus. The fungus Neurospora crassa has a specific mutant known as Poky. This mutant is characterized by slow growth and defects in mitochondrial ribosome assembly. It also shows deficiencies in several cytochromes. Early studies using genetic crosses proved that Poky is maternally inherited. Researchers eventually discovered the primary defect was a deletion in the mitochondrial DNA. Specifically, the deletion occurred in the sequence encoding the small subunit of mitochondrial ribosomal RNA. This discovery helped prove that certain genotypes are controlled by extranuclear DNA.

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File:Mitochondrion structure.svg
Mitochondrion structure.svg
File:Egg cell fertilization - Zygote.png
Egg cell fertilization - Zygote.png
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