Polyelectrolyte theory of the gene

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The polyelectrolyte theory of the gene proposes that for a linear genetic biopolymer dissolved in water, such as DNA, to undergo Darwinian evolution anywhere in the universe, it must be a polyelectrolyte, a polymer containing repeating ionic charges. [1] These charges maintain the uniform physical properties needed for Darwinian evolution, regardless of the information encoded in the genetic biopolymer. [1] [2] [3] DNA is such a molecule. Regardless of its nucleic acid sequence, the negative charges on its backbone dominate the physical interactions of the molecule to such a degree that it maintains uniform physical properties such as its aqueous solubility and double-helix structure. [1]

Contents

The polyelectrolyte theory of the gene was proposed by Steven A. Benner and Daniel Hutter in 2002 [2] and has largely remained a theoretical framework astrobiologists have used to think about how life may be detected beyond Earth. This idea was later linked by Benner [3] [1] to Erwin Schrödinger's view of the gene as an "aperiodic crystal" [4] to make a robust, universally generalized concept of a genetic biopolymer—a biopolymer acting as a unit of inheritance in Darwinian evolution.

Benner and others who built on his work [5] have proposed methods for how to concentrate and identify genetic biopolymers on other planets and moons within the solar system using electrophoresis, which uses an electric field to concentrate charged compounds. [1] [2] [3]

Although few have tested the polyelectrolyte theory of the gene, in 2019, lab experiments challenged the universality of this idea. This work was able to create non-electrolyte polymers capable of limited Darwinian evolution, but only up to a length of 72 nucleotides. [6] [7]

Physical structure of polyelectrolytes

The phosphodiester linkages link nucleotides together and form the negatively charged backbone of DNA and RNA. Phosphodiester Bond Diagram.svg
The phosphodiester linkages link nucleotides together and form the negatively charged backbone of DNA and RNA.

A polyelectrolyte is a polymer with repeating electrostatically charged units. In the context of the polyelectrolyte theory of the gene, this polyelectrolyte is a biopolymer—a polymer derived from a living system—with a repeated ionically charged unit, similar to the genetic biopolymer in modern biology, DNA. Although RNA does not act as a genetic biopolymer archive in modern biology—except in the case of some viruses such as coronavirus [8] and HIV [9] —the RNA World hypothesis suggests that RNA may have preceded DNA as life’s first genetic biopolymer. [10] The nucleotide building blocks that make up DNA and RNA are connected by negatively charged phosphate groups. These phosphodiester linkages create the repeating negative charges on the molecule’s backbone that give DNA and RNA their polyelectrolyte nature. [11]

Polyelectrolytes in the context of genetic biopolymers

To participate in Darwinian evolution, which can be described as "descent with modification", [12] a unit of inheritance must be capable of imperfect replication to occasionally produce a new modified unit of inheritance, which must still be capable of being replicated. This imperfect replication leads to the variation on which Darwinian evolution can act. [13]

The polyelectrolyte theory of the gene attempts to understand modern biology’s unit of inheritance, DNA, at a generalizable level. In 2002, Steven A. Benner and Daniel Hutter identified the repeated charges in DNA's phosphodiester linkages as crucial to its function as a genetic biopolymer. They proposed with the polyelectrolyte theory of the gene that repeated ionic charges—positive or negative—are a general requirement for all water-dissolved genetic biopolymers to undergo Darwinian evolution anywhere in the cosmos. [2]

This concept works in tandem with the view of the gene as an "aperiodic crystal" as proposed by Erwin Schrödinger in his 1944 book "What Is Life?". [4] An aperiodic crystal, as Schrödinger describes it, has a discrete set of molecular building blocks in a non-repeating arrangement. DNA is an aperiodic crystal composed of discrete nucleobases (A, T, C, and G), which are arranged based on the information they encode, not in any repeated format. While this idea of an "aperiodic crystal" was not initially linked to the polyelectrolyte theory of the gene, Benner, in later work, connected the two. [3] [1]

Polyelectrolytes remain physically uniform regardless of the information encoded

A graphical representation of a DNA double helix. DNA Visual Representation of Double-Helix.png
A graphical representation of a DNA double helix.

In biochemistry, the structure of a biomolecule dictates its function, and therefore changes in structure cause changes in function. [14] To work as a unit of inheritance, the genetic biopolymer must maintain shape and, therefore, physical and chemical consistency, regardless of the information the structure encodes. DNA is such a molecule. No matter what the nucleic acid sequence is, DNA maintains a consistent double helix structure and, therefore, the consistent physical properties that allow it to remain dissolved in water and be replicated by cellular machinery. The polyelectrolyte theory of the gene reasons that DNA can maintain its shape regardless of mutations because the negative charges on the phosphate backbone dominate the physical interactions of the molecule to such a degree that changes in the nucleic acid sequence, the encoded information, do not affect the overall physical behavior of the molecule. [2]

For example, thymidine nucleotides (T) are very soluble in water while guanosine nucleotides (G) are more insoluble; however, an oligonucleotide—a short polynucleotide sequence—composed of only thymine and one composed of only guanine has the same overall structure and physical properties. [15] If changes in the nucleic acid sequence, which encodes genetic information, change the physical properties of DNA, these changes could break down the mechanism by which DNA replicates.

This physical uniformity is very rare in nature. Take another biopolymer, for example, proteins. The nucleic acid sequence in DNA codes for the sequence of amino acids that make up proteins. A change to even a single amino acid in the primary sequence of a protein can completely change the physical properties of that protein. For example, the sickle-cell trait is caused by a single mutation of an adenine to a thymine in the hemoglobin gene, causing a switch from a glutamic acid to a valine. [16] This completely changes the three-dimensional structure of hemoglobin and thus changes the physical properties of the protein that lead to the sickle-cell trait.

Proteins are sensitive to changes in amino acid sequence because the 20 different amino acid side chains form bonds and partial bonds with each other. [17] In addition, the protein backbone has a dipole moment—having partially positive and partially negative sides—which can further create interactions within the molecule. These side-chain and backbone interactions are sensitive to changes in the environment and amino acid sequence. It is unlikely that a protein could act as a genetic biomolecule because changes in amino acid sequence lead to changes in overall physical structure and properties. [2]

Another non-electrolyte biopolymer would suffer the same challenges as a protein when acting as a genetic biomolecule. Changes in physical properties with changes in encoded information would mean that such a molecule would struggle to be replicated with certain sequences of encoded information, as those sequences would result in physical properties incompatible with replication. This problem means that the hypothetical protein gene would not be able to explore all possible genetic sequences, as certain sequences would cause the molecule to fail to be replicated based on the physical structure of its gene, not on the fitness of what the gene codes for. [2]

Benner and Hutter initially described this property of DNA as being "capable of surviving modifications in constitution without loss of properties essential for replication" or the acronym COSMIC-LOPER. This acronym gives scientists a shorthand way of describing the complex idea of a genetic biopolymer having the physical uniformity regardless of encoded information that allows it to be replicated. [2]

Although RNA is often described as a genetic biopolymer because of its theorized role as life’s first unit of inheritance (RNA World), it is not entirely COSMIC-LOPER. RNA, especially sequences high in guanine (G), is capable of folding and performing enzyme-type chemistry. [2] [18] Folding in guanine-rich RNA sequences prevents the templating ability of RNA and thus its ability to be replicated in an RNA-world scenario, for the same reason it would be difficult for a protein-based gene to replicate. [2]

Repeated ionic charges increase solubility in water

The repeated negative charges increase the solubility of DNA and RNA in water. Because ionic charges are highly soluble in water, having them on the molecule's backbone increases the molecule's solubility. [19] If the backbone of a hypothetical genetic biopolymer were linked together in a non-ionic fashion, the solubility of the whole molecule would decrease. [20] Solubility is important because, in order to be replicated, DNA—or any other genetic biomolecule—must be soluble to interact with replicative machinery. [11]

Repeated ionic charges promote Watson–Crick base pairing specificity

The Watson-Crick edge Edge of Interaction on Nucleoside.png
The Watson–Crick edge

The repeated negative charges of the DNA backbone electrostatically repel each other, preventing interactions both within and between DNA strands. This repulsion promotes specific interactions along the Watson–Crick 'edge' of the nucleobases, promoting Watson–Crick base pairing specificity—A pairs with T and C pairs with G. [2]

Repeated ionic charges prevent folding

Polyelectrolyte biopolymers tend towards linearity due to like-charge repulsive interactions on the backbone. DNA, for example, tends towards linearity due to repulsive interactions between the negative charges of its phosphodiester-linked backbone. Neutral biopolymers tend to fold and aggregate due to the lack of like-charge repulsive interactions. Folding is generally a favorable process in neutral biopolymers because it creates favorable intramolecular interactions. For example, proteins tend to fold because this produces favorable interactions between the dipole moments of the backbone, between complementary amino acid side chains, and the exchange of unfavorable hydrophilic-hydrophobic interactions for favorable hydrophobic-hydrophobic interactions of the protein core. Polyelectrolyte v neutral biopolymer.jpg
Polyelectrolyte biopolymers tend towards linearity due to like-charge repulsive interactions on the backbone. DNA, for example, tends towards linearity due to repulsive interactions between the negative charges of its phosphodiester-linked backbone. Neutral biopolymers tend to fold and aggregate due to the lack of like-charge repulsive interactions. Folding is generally a favorable process in neutral biopolymers because it creates favorable intramolecular interactions. For example, proteins tend to fold because this produces favorable interactions between the dipole moments of the backbone, between complementary amino acid side chains, and the exchange of unfavorable hydrophilic-hydrophobic interactions for favorable hydrophobic-hydrophobic interactions of the protein core.

The repeated negative charges on the backbone keep DNA and many RNA molecules from folding and allow them to act as templates. In water, molecules take on a conformation that is the most energetically favorable, with the lowest Gibbs free energy. [11] This configuration maximizes favorable interactions (hydrogen bonding, positive-negative charge interactions, van der Waals interactions) and minimizes unfavorable interactions (i.e., hydrophilic-hydrophobic interactions and like charge interactions). In the case of double-stranded DNA and RNA, the most energetically favorable form is the linear double helix configuration because it maximizes interactions between base pairs and between the negatively charged backbone and the surrounding water molecules while minimizing interactions between the negatively charged phosphodiester linkages of the backbone. [11] If the double-stranded DNA or RNA molecule folded, it would exchange favorable water-backbone interactions for unfavorable backbone-backbone interactions. A biopolymer without an ionically charged backbone, like proteins, would not produce unfavorable backbone-backbone interaction during folding and thus would readily fold and aggregate. This inherent tendency towards linearity improves DNA’s ability to act as a template for replication [2] because folded and aggregated conformations are inaccessible to replication machinery.

Lab experiments

Lab experiments conducted with non-electrolyte analogs of DNA and RNA initially inspired Benner and Hutton to publish on the polyelectrolyte theory of the gene. [3] During the late ‘80s and '90s, scientists developed synthetic DNA-like molecules to bind to and silence unwanted mRNA gene products as a way to treat disease. [2] [21] As part of this exploratory research, researchers developed a variety of non-electrolyte RNA and DNA analogs that would be able to cross the cell membrane, which DNA and RNA are incapable of doing because of their charged backbones. One of these analogs substituted a sulfone (SO₂) for the natural phosphodiester (PO₂⁻) linkage. While initial experiments showed the sulfone analog to have very similar properties to DNA as a dimer—two nucleotides linked together—when longer sulfone analogs were synthesized, they folded, lost Watson–Crick base pair specificity, and had dramatic changes in physical properties due to small changes in nucleic acid sequence. [2] The reduction in the quality of the traits that make DNA a good genetic molecule was seen with all the nonionic linkers that were tested as of 2002. [2]

The closest non-electrolyte analog to maintaining the qualities of DNA was the polyamide-linked nucleic acid analog (PNA), which replaced the phosphodiester linkage of DNA with an uncharged N-(2-aminoethyl)glycine linkage. Even Benner and Hutter questioned if PNA might disprove their polyelectrolyte hypothesis; however, even though PNA maintained the qualities of DNA up to a length of 20 nucleotides, beyond that length, the molecules started to lose Watson–Crick base pair specificity, aggregated, and became sensitive to changes in nucleic acid sequence. [2]

Lab experiments that challenge the polyelectrolyte theory of the gene

In 2019, a group led by Philipp Holliger in Cambridge, England, developed non-electrolyte P-alkylphosphonate nucleic acids (phNA) DNA analogs that were able to undergo templated synthesis and directed evolution. [22] The phNA analogs substituted the charged oxygen on DNA’s phosphate backbone with an uncharged methyl or ethyl group. While other DNA analogs have been shown to undergo templated synthesis and directed evolution, this discovery was the first time a non-electrolyte DNA analog had been shown to have these properties and the first time the polyelectrolyte theory of the gene had been experimentally challenged. [23] However, the Template-directed synthesis of phNA was only performed up to a length of 72 nucleotides. [22] This is around the length of the shortest naturally occurring gene, tRNA, [24] but is roughly an order of magnitude shorter than the genome of the smallest free-living organism. [25] The human genome for reference is 3.05×10⁹ base pairs long. [26]

As an "agnostic biosignature"

Since its inception, the polyelectrolyte theory of the gene has been put in the context of searching for life in the universe. This theory, combined with Schrödinger's view of a gene as an aperiodic crystal, provides a so-called "agnostic biosignature", [1] a sign of life that does not presuppose any biochemistry. [27] In other words, a generalized view of life should hold anywhere in the universe. [1]

Since the theorized genetic polyelectrolyte biomolecules could be charged either positively or negatively, as in the case of DNA and RNA, they can be concentrated in water with an electric field using electrophoresis or electrodialysis. This hypothetical concentration device has been called an agnostic life-finding device. [1] Similar to how electrophoresis works to separate DNA molecules, negatively charged molecules, like DNA or RNA, would be attracted to a positively charged anode, and positively charged genetic biomolecules would be attracted to a negatively charged cathode. [15]

Once the polyelectrolyte biomolecule has been concentrated, Benner suggests the molecules be tested for size and shape uniformity. In addition, the molecules should be tested for the use of a limited number of building blocks arranged in a non-repeating fashion, an aperiodic crystal structure. [1] Benner has suggested that this could be done using matrix-assisted laser desorption ionization (MALDI) paired with an orbitrap high-resolution mass spectrometer. [28] Another suggested approach has been to use nanopore sequencing technology, although questions of whether the solar radiation experienced during transit and on-site would affect the functionality of the device remain. [5] While space agencies have yet to use any of these proposed systems for life detection, they may be used in the future on Mars, [28] Enceladus, [1] and Europa. [5]

Despite the polyelectrolyte theory of the gene and the aperiodic crystal view of the gene being described as agnostic biosignatures, these theories are terra-, or earth-life, centric. It is unknown what life on another world might be; while it is often stated that life of any kind needs biomolecules and water, this may not be true. [19]

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References

  1. 1 2 3 4 5 6 7 8 9 10 11 Benner, Steven A. (2017). "Detecting Darwinism from Molecules in the Enceladus Plumes, Jupiter's Moons, and Other Planetary Water Lagoons". Astrobiology. 17 (9): 840–851. Bibcode:2017AsBio..17..840B. doi:10.1089/ast.2016.1611. ISSN   1531-1074. PMC   5610385 . PMID   28665680.
  2. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 Benner, Steven A.; Hutter, Daniel (2002-02-01). "Phosphates, DNA, and the Search for Nonterrean Life: A Second Generation Model for Genetic Molecules". Bioorganic Chemistry. 30 (1): 62–80. doi:10.1006/bioo.2001.1232. ISSN   0045-2068. PMID   11955003.
  3. 1 2 3 4 5 Benner, Steven A. (2023-02-27). "Rethinking nucleic acids from their origins to their applications". Philosophical Transactions of the Royal Society B: Biological Sciences. 378 (1871). doi:10.1098/rstb.2022.0027. ISSN   0962-8436. PMC   9835595 . PMID   36633284.
  4. 1 2 Schrödinger, Erwin (1944). What is Life? The Physical Aspect of the Living Cell. United Kingdom: Cambridge University. ISBN   0-521-42708-8.
  5. 1 2 3 Sutton, Mark A.; Burton, Aaron S.; Zaikova, Elena; Sutton, Ryan E.; Brinckerhoff, William B.; Bevilacqua, Julie G.; Weng, Margaret M.; Mumma, Michael J.; Johnson, Sarah Stewart (2019-03-29). "Radiation Tolerance of Nanopore Sequencing Technology for Life Detection on Mars and Europa". Scientific Reports. 9 (1): 5370. Bibcode:2019NatSR...9.5370S. doi:10.1038/s41598-019-41488-4. ISSN   2045-2322. PMC   6441015 . PMID   30926841.
  6. ↑ Brown, Asha; Brown, Tom (2019). "Curtailing their negativity". Nature Chemistry. 11 (6): 501–503. Bibcode:2019NatCh..11..501B. doi: 10.1038/s41557-019-0274-1 . ISSN   1755-4349. PMID   31123348. S2CID   163166821.
  7. ↑ Arangundy-Franklin, Sebastian; Taylor, Alexander I.; Porebski, Benjamin T.; Genna, Vito; Peak-Chew, Sew; Vaisman, Alexandra; Woodgate, Roger; Orozco, Modesto; Holliger, Philipp (2019). "A synthetic genetic polymer with an uncharged backbone chemistry based on alkyl phosphonate nucleic acids". Nature Chemistry. 11 (6): 533–542. Bibcode:2019NatCh..11..533A. doi:10.1038/s41557-019-0255-4. ISSN   1755-4349. PMC   6542681 . PMID   31011171.
  8. ↑ Brant, Ayslan Castro; Tian, Wei; Majerciak, Vladimir; Yang, Wei; Zheng, Zhi-Ming (2021). "SARS-CoV-2: From its discovery to genome structure, transcription, and replication". Cell & Bioscience. 11 (1): 136. doi: 10.1186/s13578-021-00643-z . PMC   8287290 . PMID   34281608.
  9. ↑ Harwig, Alex; Das, Atze T.; Berkhout, Ben (2015). "HIV-1 RNAs: sense and antisense, large mRNAs and small siRNAs and miRNAs". Current Opinion in HIV and AIDS. 10 (2): 103–109. doi:10.1097/COH.0000000000000135. ISSN   1746-630X. PMID   25565176. S2CID   34885126.
  10. ↑ RNA World
  11. 1 2 3 4 Nelson, David L.; Cox, Michael M.; Nelson, David L. (2013). Lehninger, Albert L. (ed.). Lehninger principles of biochemistry (Sixth ed.). Basingstoke: Macmillan Higher Education. ISBN   978-1-4292-3414-6.
  12. ↑ Bromham, Lindell (2016-01-21), "Selection", An Introduction to Molecular Evolution and Phylogenetics, Oxford University Press, doi:10.1093/hesc/9780198736363.003.0007, ISBN   978-0-19-873636-3 , retrieved 2023-12-09
  13. ↑ Gregory, T. Ryan (2009). "Understanding Natural Selection: Essential Concepts and Common Misconceptions". Evolution: Education and Outreach. 2 (2): 156–175. doi: 10.1007/s12052-009-0128-1 . ISSN   1936-6434. S2CID   4508223.
  14. ↑ "2.3: Structure & Function- Proteins I". Biology LibreTexts. 2017-01-21. Retrieved 2023-12-05.
  15. 1 2 Benner, Steven A. "Making Operational the Polyelectrolyte Theory of the Gene in the Agnostic Search for Martian Life – The Primordial Scoop" . Retrieved 2023-12-05.
  16. ↑ "Genetic Mutation | Learn Science at Scitable". www.nature.com. Retrieved 2023-12-07.
  17. ↑ "Protein Folding". Chemistry LibreTexts. 2013-10-02. Retrieved 2023-12-07.
  18. ↑ Talini, Giulia; Branciamore, Sergio; Gallori, Enzo (2011). "Ribozymes: Flexible molecular devices at work". Biochimie. 93 (11): 1998–2005. doi:10.1016/j.biochi.2011.06.026. PMID   21740954.
  19. 1 2 Benner, Steven A. (2010). "Defining Life". Astrobiology. 10 (10): 1021–1030. Bibcode:2010AsBio..10.1021B. doi:10.1089/ast.2010.0524. ISSN   1531-1074. PMC   3005285 . PMID   21162682.
  20. ↑ "4.5: Solubility of Ionic Compounds". Chemistry LibreTexts. 2022-01-20. Retrieved 2023-12-07.
  21. ↑ Crooke, Stanley T. (2000), "Progress in antisense technology: The end of the beginning", Antisense Technology Part A: General Methods, Methods of Delivery, and RNA Studies, Methods in Enzymology, vol. 313, Elsevier, pp. 3–45, doi:10.1016/s0076-6879(00)13003-4, ISBN   978-0-12-182214-9, PMID   10595347 , retrieved 2023-12-07
  22. 1 2 Arangundy-Franklin, Sebastian; Taylor, Alexander I.; Porebski, Benjamin T.; Genna, Vito; Peak-Chew, Sew; Vaisman, Alexandra; Woodgate, Roger; Orozco, Modesto; Holliger, Philipp (2019). "A synthetic genetic polymer with an uncharged backbone chemistry based on alkyl phosphonate nucleic acids". Nature Chemistry. 11 (6): 533–542. Bibcode:2019NatCh..11..533A. doi:10.1038/s41557-019-0255-4. ISSN   1755-4330. PMC   6542681 . PMID   31011171.
  23. ↑ Brown, Asha; Brown, Tom (2019). "Curtailing their negativity". Nature Chemistry. 11 (6): 501–503. Bibcode:2019NatCh..11..501B. doi: 10.1038/s41557-019-0274-1 . ISSN   1755-4330. PMID   31123348. S2CID   163166821.
  24. ↑ Krahn, Natalie; Fischer, Jonathan T.; Söll, Dieter (2020). "Naturally Occurring tRNAs With Non-canonical Structures". Frontiers in Microbiology. 11. doi: 10.3389/fmicb.2020.596914 . ISSN   1664-302X. PMC   7609411 . PMID   33193279.
  25. ↑ Giovannoni, Stephen J.; Tripp, H. James; Givan, Scott; Podar, Mircea; Vergin, Kevin L.; Baptista, Damon; Bibbs, Lisa; Eads, Jonathan; Richardson, Toby H.; Noordewier, Michiel; Rappé, Michael S.; Short, Jay M.; Carrington, James C.; Mathur, Eric J. (2005-08-19). "Genome Streamlining in a Cosmopolitan Oceanic Bacterium". Science. 309 (5738): 1242–1245. Bibcode:2005Sci...309.1242G. doi:10.1126/science.1114057. ISSN   0036-8075. PMID   16109880. S2CID   16221415.
  26. ↑ Nurk, Sergey; Koren, Sergey; Rhie, Arang; Rautiainen, Mikko; Bzikadze, Andrey V.; Mikheenko, Alla; Vollger, Mitchell R.; Altemose, Nicolas; Uralsky, Lev; Gershman, Ariel; Aganezov, Sergey; Hoyt, Savannah J.; Diekhans, Mark; Logsdon, Glennis A.; Alonge, Michael (2022). "The complete sequence of a human genome". Science. 376 (6588): 44–53. Bibcode:2022Sci...376...44N. doi:10.1126/science.abj6987. ISSN   0036-8075. PMC   9186530 . PMID   35357919.
  27. ↑ "NASA Astrobiology". astrobiology.nasa.gov. Retrieved 2023-12-07.
  28. 1 2 Špaček, Jan; Benner, Steven A. (2022-10-01). "Agnostic Life Finder (ALF) for Large-Scale Screening of Martian Life During In Situ Refueling". Astrobiology. 22 (10): 1255–1263. Bibcode:2022AsBio..22.1255S. doi:10.1089/ast.2021.0070. ISSN   1531-1074. PMID   35796703. S2CID   250336451.
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