Nuclear gene

A nuclear gene is a gene that has its DNA nucleotide sequence physically situated within the cell nucleus of a eukaryotic organism. This term is employed to differentiate nuclear genes, which are located in the cell nucleus, from genes that are found in mitochondria or chloroplasts. The vast majority of genes in eukaryotes are nuclear.

Nuclear gene location

Endosymbiotic theory

Mitochondria and plastids evolved from free-living prokaryotes into current cytoplasmic organelles through endosymbiotic evolution.^[1] Mitochondria are thought to be necessary for eukaryotic life to exist. They are known as the cell's powerhouses because they provide the majority of the energy or ATP required by the cell. The mitochondrial genome (mtDNA) is replicated separately from the host genome. Human mtDNA codes for 13 proteins, most of which are involved in oxidative phosphorylation (OXPHOS). The nuclear genome encodes the remaining mitochondrial proteins, which are then transported into the mitochondria.^[2] The genomes of these organelles have become far smaller than those of their free-living predecessors. This is mostly due to the widespread transfer of genes from prokaryote progenitors to the nuclear genome, followed by their elimination from organelle genomes. In evolutionary timescales, the continuous entry of organelle DNA into the nucleus has provided novel nuclear genes.^[1] Furthermore, Mitochondria depend on nuclear genes for essential protein production as they cannot generate all necessary proteins independently.^[3]

Endosymbiotic organelle interactions

Though separated from one another within the cell, nuclear genes and those of mitochondria and chloroplasts can affect each other in a number of ways. Nuclear genes play major roles in the expression of chloroplast genes and mitochondrial genes.^[4] Additionally, gene products of mitochondria can themselves affect the expression of genes within the cell nucleus.^[5] This can be done through metabolites as well as through certain peptides trans-locating from the mitochondria to the nucleus, where they can then affect gene expression.^[6][7][8]

Structure

Eukaryotic genomes have distinct higher-order chromatin structures that are closely packaged functional relates to gene expression. Chromatin compresses the genome to fit into the cell nucleus, while still ensuring that the gene can be accessed when needed, such as during gene transcription, replication, and DNA repair.^[9] The entirety of genome function is based on the underlying relationship between nuclear organization and the mechanisms involved in genome organization, in which there are a number of complex mechanisms and biochemical pathways which can affect the expression of individual genes within the genome.^[9] The remaining mitochondrial proteins, metabolic enzymes, DNA and RNA polymerases, ribosomal proteins, and mtDNA regulatory factors are all encoded by nuclear genes. Because nuclear genes constitute the genetic foundation of all eukaryotic organisms, anything that might change their genetic expression has a direct impact on the organism's cellular genotypes and phenotypes.^[2] The nucleus also contains a number of distinct subnuclear foci known as nuclear bodies, which are dynamically controlled structures that help numerous nuclear processes run more efficiently.^[9] Active genes, for instance, might migrate from chromosomal regions and concentrate into subnuclear foci known as transcription factories.^[9]

Protein synthesis

The majority of proteins in a cell are the product of messenger RNA transcribed from nuclear genes, including most of the proteins of the organelles, which are produced in the cytoplasm like all nuclear gene products and then transported to the organelle. Genes in the nucleus are arranged in a linear fashion upon chromosomes, which serve as the scaffold for replication and the regulation of gene expression. As such, they are usually under strict copy-number control, and replicate a single time per cell cycle.^[10] Nuclear cells such as platelets do not possess nuclear DNA and therefore must have alternative sources for the RNA that they need to generate proteins. With the nuclear genome's 3.3 billion DNA base pairs in humans, one good example of a nuclear gene is MDH1 or the malate dehydrogenase 1 gene. In various metabolic pathways, including the citric acid cycle, MDH1 is a protein-coding gene that encodes an enzyme that catalyzes the NAD/NADH-dependent, reversible oxidation of malate to oxaloacetate. This gene codes for the cytosolic isozyme, which is involved in the malate-aspartate shuttle, which allows malate to cross past the mitochondrial membrane and be converted to oxaloacetate to perform further cellular functions.^[11] This gene among many exhibits its huge purposeful role in the entirety of an organism’s physiologic function. Although non-nuclear genes may exist in its functional nature, the role of nuclear genes in response and in coordination with non-nuclear genes is fundamental.

Significance

Many nuclear-derived transcription factors have played a role in respiratory chain expression. These factors may have also contributed to the regulation of mitochondrial functions. Nuclear respiratory factor (NRF-1) fuses to respiratory encoding genes proteins, to the rate-limiting enzyme in biosynthesis, and to elements of replication and transcription of mitochondrial DNA, or mtDNA. The second nuclear respiratory factor (NRF-2) is necessary for the production of cytochrome c oxidase subunit IV (COXIV) and Vb (COXVb) to be maximized.^[4]

The studying of gene sequences for the purpose of speciation and determining genetic similarity is just one of the many uses of modern day genetics, and the role that both types of genes have in that process is important. Though both nuclear genes and those within endosymbiotic organelles provide the genetic makeup of an organism, there are distinct features that can be better observed when looking at one compared to the other. Mitochondrial DNA is useful in the study of speciation as it tends to be the first to evolve in the development of a new species, which is different from nuclear genes' chromosomes that can be examined and analyzed individually, each giving its own potential answer as to the speciation of a relatively recently evolved organism.^[12]

Low-copy nuclear genes in plants are valuable for improving phylogenetic reconstructions, especially when universal markers like Chloroplast DNA, or cpDNA and Nuclear ribosomal DNA, or nrDNA fall short. Challenges in using these genes include limited universal markers and the complexity of gene families. Nonetheless, they are essential for resolving close species relationships and understanding plant phylogenetic studies. While using low-copy nuclear genes requires additional lab work, advances in sequencing and cloning techniques have made it more accessible. Fast-evolving introns in these genes can offer crucial phylogenetic insights near species boundaries. This approach, along with the analysis of developmentally important genes, enhances the study of plant diversity and evolution.^[13]

As nuclear genes are the genetic basis of all eukaryotic organisms, anything that can affect their expression therefore directly affects characteristics about that organism on a cellular level. The interactions between the genes of endosymbiotic organelles like mitochondria and chloroplasts are just a few of the many factors that can act on the nuclear genome.

References

1. Timmis JN, Ayliffe MA, Huang CY, Martin W (February 2004). "Endosymbiotic gene transfer: organelle genomes forge eukaryotic chromosomes". Nature Reviews Genetics. 5 (2): 123–135. doi:10.1038/nrg1271. ISSN 1471-0056. PMID 14735123. S2CID 2385111.
2. Annesley SJ, Fisher PR (2019-07-05). "Mitochondria in Health and Disease". Cells. 8 (7): 680. doi:10.3390/cells8070680. ISSN 2073-4409. PMC 6678092. PMID 31284394.
3. "mtDNA and Mitochondrial Diseases | Learn Science at Scitable". www.nature.com. Retrieved 2023-12-09.
4. Herrin DL, Nickelsen J (2004). "Chloroplast RNA processing and stability". Photosynthesis Research. 82 (3): 301–14. Bibcode:2004PhoRe..82..301H. doi:10.1007/s11120-004-2741-8. PMID 16143842. S2CID 37108218.
5. Ali AT, Boehme L, Carbajosa G, Seitan VC, Small KS, Hodgkinson A (February 2019). "Nuclear genetic regulation of the human mitochondrial transcriptome". eLife. 8. doi:10.7554/eLife.41927. PMC 6420317. PMID 30775970.
6. Fetterman JL, Ballinger SW (August 2019). "Mitochondrial genetics regulate nuclear gene expression through metabolites". Proceedings of the National Academy of Sciences of the United States of America. 116 (32): 15763–15765. Bibcode:2019PNAS..11615763F. doi:10.1073/pnas.1909996116. PMC 6689900. PMID 31308238.
7. Kim KH, Son JM, Benayoun BA, Lee C (September 2018). "The Mitochondrial-Encoded Peptide MOTS-c Translocates to the Nucleus to Regulate Nuclear Gene Expression in Response to Metabolic Stress". Cell Metabolism. 28 (3): 516–524.e7. doi:10.1016/j.cmet.2018.06.008. PMC 6185997. PMID 29983246.
8. Mangalhara KC, Shadel GS (September 2018). "A Mitochondrial-Derived Peptide Exercises the Nuclear Option". Cell Metabolism. 28 (3): 330–331. doi:10.1016/j.cmet.2018.08.017. PMID 30184481.
9. Van Bortle K, Corces VG (2012). "Nuclear organization and genome function". Annual Review of Cell and Developmental Biology. 28: 163–87. doi:10.1146/annurev-cellbio-101011-155824. PMC 3717390. PMID 22905954.
10. Griffiths AJ, Gelbart WM, Miller JH, Lewontin RC (1999). "DNA Replication". Modern Genetic Analysis. New York: W. H. Freeman.
11. Mcalister-Henn L, Curtis Small W (1997), Molecular Genetics of Yeast TCA Cycle Isozymes, Progress in Nucleic Acid Research and Molecular Biology, vol. 57, Elsevier, pp. 317–339, doi:10.1016/s0079-6603(08)60285-8, ISBN 978-0-12-540057-2, PMID 9175438, retrieved 2021-11-18
12. Moore WS (1995). "Inferring Phylogenies from mtDNA Variation: Mitochondrial-Gene Trees Versus Nuclear-Gene Trees". Evolution. 49 (4): 718–726. doi:10.2307/2410325. JSTOR 2410325. PMID 28565131.
13. Sang T (2002). "Utility of low-copy nuclear gene sequences in plant phylogenetics". Critical Reviews in Biochemistry and Molecular Biology. 37 (3): 121–147. doi:10.1080/10409230290771474. ISSN 1040-9238. PMID 12139440.