The discovery that \(M .\) genitalium has a genome of \(0.58 \mathrm{Mb}\) and only 470 protein-coding genes has sparked interest in determining the minimum number of genes needed for a living cell. In the search for organisms with smaller and smaller genomes, a new species of Archaea, Nanoarchaeum equitans, was discovered in a high-temperature vent on the ocean floor. This prokaryote has one of the smallest cell sizes ever discovered, and its genome is only about 0.5 Mb. However, organisms such as \(M .\) genitalium, N. equitans, and other microbes with very small genomes are either parasites or symbionts. How does this affect the search for a minimum genome? Should the definition of the minimum genome size for a living cell be redefined?

Short Answer

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Answer: The status of prokaryotes with smaller genomes as parasites or symbionts affects the search for a minimum genome size for a living cell because these organisms often rely on their host organisms for survival, which could mean their reduced genomes lack genes necessary for independent survival. This might not provide an accurate representation of the minimum genes required for a self-sufficient, non-parasitic or non-symbiotic living cell. To obtain a better understanding of the minimum genome size, the focus should be on free-living organisms with the smallest genomes.

Step by step solution

01

Introduction

The minimum genome size refers to the smallest number of genes required for a living cell to function. The discovery of smaller and smaller genomes raises questions about what constitutes a minimum genome and whether these tiny organisms should be considered when determining the minimum genome size for a living cell.
02

Factors Affecting Genome Size

Organisms with very small genomes, such as M. genitalium and N. equitans, are often parasites or symbionts. A parasite is an organism that lives on or in another organism, causing harm to its host. A symbiont, on the other hand, is an organism that lives in close association with another organism, often benefiting both parties. The fact that these microorganisms have reduced genome sizes while living in association with other organisms leads to questions about their self-sufficiency and whether their genomes provide an accurate representation of a minimum genome size for a standalone living cell.
03

Dependency on Host Organisms

Since these microbes with small genomes often rely on their host organisms, their genomes might have lost genes that would be necessary for independent survival. This means that their reduced genome sizes might not provide a true picture of the minimum genes required for a self-sufficient, non-parasitic or non-symbiotic living cell. In other words, their extremely reduced genomes might represent the minimum genes needed for survival within their specific ecological niche, rather than in a general context.
04

Redefining the Minimum Genome Size

In light of these considerations, it might be necessary to redefine the minimum genome size for a living cell. The definition should take into account the genes required for independent survival, rather than focusing solely on organisms with the smallest known genomes. A more relevant approach might involve studying free-living organisms with the smallest genomes, which could offer better insights into the minimum number of genes needed for a self-sufficient living cell.
05

Conclusion

The discovery of organisms like M. genitalium and N. equitans with very small genomes has sparked interest in the search for the minimum genome size for a living cell. However, since these organisms are either parasites or symbionts and rely on their host organisms for survival, their reduced genome sizes might not represent the true minimum genome size for a standalone living cell. Redefining the minimum genome size by focusing on self-sufficient organisms with small genomes might provide a better understanding of the genetic requirements for a living cell to function independently.

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Most popular questions from this chapter

Systems biology models the complex networks of interacting genes, proteins, and other molecules that contribute to human genetic diseases, such as cancer, diabetes, and hypertension. These interactomes show the contribution of each piece towards the whole and where diseases overlap, and provide models for drug discovery and development. Describe some tions (Roy et al., 2008 ). In some cases, closely related homologs may engender completely different classes of proteins (enzymes). Consider the 3 D structure of two proteins with 60 percent homology with entirely different functions. Explain how different functions may evolve by discussing the position of the homologous amino acid track, its relation to nonhomologous tracks, and the role that chaperones (Chapter 14) may play in determining protein function. of the differences that might be seen in the interactomes of normal and cancerous cells taken from the same tissue, and explain how these differences could lead to drugs specifically targeted against cancer cells.

What is bioinformatics, and why is this discipline essential for studying genomes? Provide two examples of bioinformatics applications.

Traditionally, gene sequence homology implied functional similarity. Even though two proteins may contain over 60 percent sequence identity, only about 38 percent have identical functions (Roy et al., 2008 ). In some cases, closely related homologs may engender completely different classes of proteins (enzymes). Consider the 3 D structure of two proteins with 60 percent homology with entirely different functions. Explain how different functions may evolve by discussing the position of the homologous amino acid track, its relation to nonhomologous tracks, and the role that chaperones (Chapter 14 ) may play in determining protein function.

What is noncoding RNA? What is its function?

Homology can be defined as the presence of common structures because of shared ancestry. Homology can involve genes, proteins, or anatomical structures. As a result of "descent with modification," many homologous structures have adapted different purposes. (a) List three anatomical structures in vertebrates that are homologous but have different functions. (b) Is it likely that homologous proteins from different species have the same or similar functions? Explain. (c) Under what circumstances might one expect proteins of similar function to not share homology? Would you expect such proteins to be homologous at the level of DNA sequences?

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