Astrobiology. Charles S. Cockell
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Название: Astrobiology

Автор: Charles S. Cockell

Издательство: John Wiley & Sons Limited

Жанр: Физика

Серия:

isbn: 9781119550396

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СКАЧАТЬ paradox is explained by non-coding DNA.

      The process of reading DNA to RNA to protein is sometimes called the “central dogma of molecular biology” (Figure 5.13). The word “dogma” is always a troubling word in science, but the overall scheme broadly shows the two fundamental steps of reading the genetic code. The word dogma was used to capture the observation that once genetic information is turned into protein, it cannot go in the reverse direction. The information in protein is not transferred back into nucleic acid in any known life.

Flow diagram starting from DNA to RNA via transcription and to protein via translation.

       Figure 5.13 A summary of the two steps in reading from DNA to RNA to protein.

      5.6.3 A Remarkable Code

      There are a few remarkable things about this process worth mentioning. First, the table of codons shown in Figure 5.12, bar some minor modifications in some organisms, is essentially universal to all life forms. This not only shows the great antiquity of the genetic code, but also strongly suggests that all life on Earth was derived from a single common ancestor in which this code first emerged, presumably from more simple codes and structures that preceded it.

      Second, the table is astounding because it is a code that allows a one-dimensional piece of information – the strand of a DNA molecule – to be transformed into the three-dimensional structure of a chemically active molecule. How did the structures emerge and what was the evolutionary process that linked one-dimensional information storage to three-dimensional biological function? This is one of the most fascinating questions in astrobiology, linked explicitly into our attempts to understand the origin of life. We come back to this when we consider the origin of life.

      5.6.4 The Evolution of the Codons

      How did the codon table evolve? It is instructive to notice that the amino acids are bunched together in the table. This has not gone unnoticed. One early hypothesis was that this arrangement leads to the minimization of errors. If the third location in the codon, which has a certain degree of “wobble,” changes, then the amino acid in the final protein is not changed. Mathematical models show that the codon table, as constituted, can achieve this error minimization. There are also other intriguing observations. For example, arginine is able to bind directly to the RNA codes represented by the codons in the table, without the transfer RNAs. The same is true for isoleucine. Could these amino acids have once bound directly to the RNA with the transfer RNA molecules becoming adaptors between the RNA and the amino acids later? It is possible that none of these ideas is mutually exclusive. Error minimization and direct associations between codons and amino acids and other factors may all have played a role in evolving the table early in the history of life.

      Discussion Point: The Universality of the Genetic Structure and Machinery

      Eschenmoser, A. (1999). Chemical etiology of nucleic acid structure. Science 284: 2118–2124.

      Hoshika, S., Leal, N.A., Kim, M-Y. et al. (2019). Hachimoji DNA and RNA: A genetic system with eight building blocks. Science 363: 884–887.

      Malyshev, D.A., Dhami, K., Lavergne, T. et al. (2014). A semi-synthetic organism with an expanded genetic alphabet. Nature 509: 385–388.

      Piccirilli, J.A., Benner, S.A., Krauch, T. et al. (1990). Enzymatic incorporation of a new base pair into DNA and RNA extends the genetic alphabet. Nature 343: 33–37.

      Focus: Astrobiologists: Nicol Caplin

Portrait of Nicol Caplin.

      Affiliation: European Space Research and Technology Centre (ESTEC), European Space Agency (ESA), The Netherlands

      What was your first degree? Environmental Science at The University of the West of England, Bristol.

      What do you study? I work as a science coordinator (Research Fellow) for the European Space Agency in the European Space Research and Technology Centre (ESTEC) in The Netherlands. My primary role is to support research scientists and ensure that requirements for carrying out biology experiments in space are defined, understood, and met by our engineering and operations teams.

      What science questions do you address? The astrobiology experiments that I am involved in organizing address a range of physiological and morphological endpoints that can provide information about life in the universe, particularly the limits of life in extreme environments. All of the projects I am assigned to are run on the International Space Station. They can be divided into two main categories of exposure to space conditions, internal and external. The internal experiments predominantly address effects of weightlessness (microgravity) while external ones expose samples to full space conditions (albeit within Earth's magnetic field but outside of the atmosphere). Such work must be carried out in space, as many of the conditions (and a combination of them) cannot be replicated on Earth.

      How did you get involved in astrobiology research? As part of my PhD in environmental radioactivity, I studied biological effects of low-dose ionizing radiation on Earth and later, in samples that had been in space. I chose to study the effects in a well-established plant model (Arabidopsis thaliana) and used analytical techniques such as morphometrics and physiological assays that can be applied to other organisms. When searching for a postdoctoral position, I focused on trying to find a job where specialist research knowledge could be useful in examining fundamental science questions relating to various organisms in space.

      5.6.5 DNA Replication