Pub Date : 2021-02-01Epub Date: 2020-10-23DOI: 10.1007/s12064-020-00323-5
Yoan Konto-Ghiorghi, Vic Norris
The generation of a phenotypic diversity that is coherent across a bacterial population is a fundamental problem. We propose here that the DNA strand-specific segregation of certain nucleoid-associated proteins or NAPs results in these proteins being asymmetrically distributed to the daughter cells. We invoke a variety of mechanisms as responsible for this asymmetrical segregation including those based on differences between the leading and lagging strands, post-translational modifications, oligomerisation and association with membrane domains.
{"title":"Hypothesis: nucleoid-associated proteins segregate with a parental DNA strand to generate coherent phenotypic diversity.","authors":"Yoan Konto-Ghiorghi, Vic Norris","doi":"10.1007/s12064-020-00323-5","DOIUrl":"https://doi.org/10.1007/s12064-020-00323-5","url":null,"abstract":"<p><p>The generation of a phenotypic diversity that is coherent across a bacterial population is a fundamental problem. We propose here that the DNA strand-specific segregation of certain nucleoid-associated proteins or NAPs results in these proteins being asymmetrically distributed to the daughter cells. We invoke a variety of mechanisms as responsible for this asymmetrical segregation including those based on differences between the leading and lagging strands, post-translational modifications, oligomerisation and association with membrane domains.</p>","PeriodicalId":54428,"journal":{"name":"Theory in Biosciences","volume":"140 1","pages":"17-25"},"PeriodicalIF":1.1,"publicationDate":"2021-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12064-020-00323-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38522350","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-02-01DOI: 10.1007/s12064-020-00337-z
Fariba Fayazi, Elena Fimmel, Lutz Strüngmann
In the 1950s, Crick proposed the concept of so-called comma-free codes as an answer to the frame-shift problem that biologists have encountered when studying the process of translating a sequence of nucleotide bases into a protein. A little later it turned out that this proposal unfortunately does not correspond to biological reality. However, in the mid-90s, a weaker version of comma-free codes, so-called circular codes, was discovered in nature in J Theor Biol 182:45-58, 1996. Circular codes allow to retrieve the reading frame during the translational process in the ribosome and surprisingly the circular code discovered in nature is even circular in all three possible reading-frames ([Formula: see text]-property). Moreover, it is maximal in the sense that it contains 20 codons and is self-complementary which means that it consists of pairs of codons and corresponding anticodons. In further investigations, it was found that there are exactly 216 codes that have the same strong properties as the originally found code from J Theor Biol 182:45-58. Using an algebraic approach, it was shown in J Math Biol, 2004 that the class of 216 maximal self-complementary [Formula: see text]-codes can be partitioned into 27 equally sized equivalence classes by the action of a transformation group [Formula: see text] which is isomorphic to the dihedral group. Here, we extend the above findings to circular codes over a finite alphabet of even cardinality [Formula: see text] for [Formula: see text]. We describe the corresponding group [Formula: see text] using matrices and we investigate what classes of circular codes are split into equally sized equivalence classes under the natural equivalence relation induced by [Formula: see text]. Surprisingly, this is not always the case. All results and constructions are illustrated by examples.
在20世纪50年代,克里克提出了所谓的无逗号代码的概念,作为生物学家在研究将核苷酸碱基序列翻译成蛋白质的过程中遇到的帧移位问题的答案。不久之后,不幸的是,这个建议并不符合生物学的现实。然而,在90年代中期,在自然界中发现了一种弱版本的无逗号代码,即所谓的循环代码。《理论生物学杂志》182:45-58,1996。循环代码允许在核糖体的翻译过程中检索阅读框架,令人惊讶的是,在自然界中发现的循环代码甚至在所有三种可能的阅读框架中都是循环的([公式:见文本]-属性)。此外,它是极大的,因为它包含20个密码子,并且是自互补的,这意味着它由对密码子和相应的反密码子组成。在进一步的研究中,发现有216个编码与J Theor Biol 182:45-58中最初发现的编码具有相同的强性质。利用代数方法,在J Math Biol, 2004中证明了216个极大自互补(公式:见文)码类可以在一个与二面体群同构的变换群(公式:见文)的作用下被划分为27个大小相等的等价类。在这里,我们将上述发现扩展到偶数基数的有限字母表上的循环代码[公式:见文本]。我们用矩阵描述了相应的群[公式:见文],并研究了在由[公式:见文]导出的自然等价关系下,哪些类的圆码被分成大小相等的等价类。令人惊讶的是,情况并非总是如此。所有的结果和结构都通过实例加以说明。
{"title":"Equivalence classes of circular codes induced by permutation groups.","authors":"Fariba Fayazi, Elena Fimmel, Lutz Strüngmann","doi":"10.1007/s12064-020-00337-z","DOIUrl":"https://doi.org/10.1007/s12064-020-00337-z","url":null,"abstract":"<p><p>In the 1950s, Crick proposed the concept of so-called comma-free codes as an answer to the frame-shift problem that biologists have encountered when studying the process of translating a sequence of nucleotide bases into a protein. A little later it turned out that this proposal unfortunately does not correspond to biological reality. However, in the mid-90s, a weaker version of comma-free codes, so-called circular codes, was discovered in nature in J Theor Biol 182:45-58, 1996. Circular codes allow to retrieve the reading frame during the translational process in the ribosome and surprisingly the circular code discovered in nature is even circular in all three possible reading-frames ([Formula: see text]-property). Moreover, it is maximal in the sense that it contains 20 codons and is self-complementary which means that it consists of pairs of codons and corresponding anticodons. In further investigations, it was found that there are exactly 216 codes that have the same strong properties as the originally found code from J Theor Biol 182:45-58. Using an algebraic approach, it was shown in J Math Biol, 2004 that the class of 216 maximal self-complementary [Formula: see text]-codes can be partitioned into 27 equally sized equivalence classes by the action of a transformation group [Formula: see text] which is isomorphic to the dihedral group. Here, we extend the above findings to circular codes over a finite alphabet of even cardinality [Formula: see text] for [Formula: see text]. We describe the corresponding group [Formula: see text] using matrices and we investigate what classes of circular codes are split into equally sized equivalence classes under the natural equivalence relation induced by [Formula: see text]. Surprisingly, this is not always the case. All results and constructions are illustrated by examples.</p>","PeriodicalId":54428,"journal":{"name":"Theory in Biosciences","volume":"140 1","pages":"107-121"},"PeriodicalIF":1.1,"publicationDate":"2021-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12064-020-00337-z","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25318410","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-02-01Epub Date: 2021-02-15DOI: 10.1007/s12064-020-00334-2
Auni Aslah Mat Daud, Cher Qing Toh, Salilah Saidun
Anemia is a significant public health problem worldwide especially among pregnant women in low- and middle-income countries. In this study, a mathematical model of the population dynamics of anemia during pregnancy and postpartum is constructed. In the modeling process, four independent variables have been considered: (1) the numbers of nonpregnant nonanemic women, (2) anemic nonpregnant women, (3) anemic pregnant or postpartum women and (4) anemic pregnant or postpartum women with complications. The mathematical model is governed by a system of first-order ordinary differential equations. The stability analysis of the model is conducted using Routh-Hurwitz criteria. There is one nonnegative equilibrium point which is asymptotically stable. The equilibrium point obtained indicates the influential parameters that can be controlled to minimize the number of patients at each stage. The proposed model can be employed to forecast the future incidence and prevalence of the disease and appraise intervention programs.
{"title":"Mathematical modeling and analysis of anemia during pregnancy and postpartum.","authors":"Auni Aslah Mat Daud, Cher Qing Toh, Salilah Saidun","doi":"10.1007/s12064-020-00334-2","DOIUrl":"https://doi.org/10.1007/s12064-020-00334-2","url":null,"abstract":"<p><p>Anemia is a significant public health problem worldwide especially among pregnant women in low- and middle-income countries. In this study, a mathematical model of the population dynamics of anemia during pregnancy and postpartum is constructed. In the modeling process, four independent variables have been considered: (1) the numbers of nonpregnant nonanemic women, (2) anemic nonpregnant women, (3) anemic pregnant or postpartum women and (4) anemic pregnant or postpartum women with complications. The mathematical model is governed by a system of first-order ordinary differential equations. The stability analysis of the model is conducted using Routh-Hurwitz criteria. There is one nonnegative equilibrium point which is asymptotically stable. The equilibrium point obtained indicates the influential parameters that can be controlled to minimize the number of patients at each stage. The proposed model can be employed to forecast the future incidence and prevalence of the disease and appraise intervention programs.</p>","PeriodicalId":54428,"journal":{"name":"Theory in Biosciences","volume":"140 1","pages":"87-95"},"PeriodicalIF":1.1,"publicationDate":"2021-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12064-020-00334-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25376201","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-02-01Epub Date: 2020-11-03DOI: 10.1007/s12064-020-00325-3
Margherita Raineri, Erki Tammiksaar
In 1835, the meaning of the cleavage furrows in the division of frog eggs was the cause of a heated argument between the Italian naturalist Mauro Rusconi and Karl Ernst von Baer. These furrows were first described by Prévost and Dumas (Ann Sci Nat 2:100-121, 129-149, 1824b) who did not realize they cut the egg into separate masses. Rusconi (Développement de la grenouille comune depuis le moment de sa naissance jusque a son état parfait, Giusti, Milano, 1826) hypothesized a connection between the furrows and a peculiar crystallization of the content of the egg which eventually produced elementary molecules as the building blocks of the embryo. von Baer (Arch Anat Phys Wiss Med 6:481-509, 1834) was the first to establish a link between the furrows and an active process of dichotomous division he considered to be the basis for all further development and differentiation. The present paper analyses the theoretical reasons behind these divergent interpretations and focuses attention on their implications for the development of the cell theory and the conceptions of life. Prévost, Dumas and Rusconi interpreted cleavage and the whole embryonic development in the light of eighteenth-century scientific theories and the French materialism of the early nineteenth century, which explained life in terms of ordered molecular movement. Starting from other premises partly rooted in German philosophy von Baer (1834) gave a totally different picture which anticipated the cell theory and modern embryology.
{"title":"Scientific traditions in conflict: the Rusconi-von Baer controversy on the embryology of frogs and the development of the cell theory.","authors":"Margherita Raineri, Erki Tammiksaar","doi":"10.1007/s12064-020-00325-3","DOIUrl":"https://doi.org/10.1007/s12064-020-00325-3","url":null,"abstract":"<p><p>In 1835, the meaning of the cleavage furrows in the division of frog eggs was the cause of a heated argument between the Italian naturalist Mauro Rusconi and Karl Ernst von Baer. These furrows were first described by Prévost and Dumas (Ann Sci Nat 2:100-121, 129-149, 1824b) who did not realize they cut the egg into separate masses. Rusconi (Développement de la grenouille comune depuis le moment de sa naissance jusque a son état parfait, Giusti, Milano, 1826) hypothesized a connection between the furrows and a peculiar crystallization of the content of the egg which eventually produced elementary molecules as the building blocks of the embryo. von Baer (Arch Anat Phys Wiss Med 6:481-509, 1834) was the first to establish a link between the furrows and an active process of dichotomous division he considered to be the basis for all further development and differentiation. The present paper analyses the theoretical reasons behind these divergent interpretations and focuses attention on their implications for the development of the cell theory and the conceptions of life. Prévost, Dumas and Rusconi interpreted cleavage and the whole embryonic development in the light of eighteenth-century scientific theories and the French materialism of the early nineteenth century, which explained life in terms of ordered molecular movement. Starting from other premises partly rooted in German philosophy von Baer (1834) gave a totally different picture which anticipated the cell theory and modern embryology.</p>","PeriodicalId":54428,"journal":{"name":"Theory in Biosciences","volume":"140 1","pages":"45-75"},"PeriodicalIF":1.1,"publicationDate":"2021-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12064-020-00325-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38668585","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-02-01Epub Date: 2021-01-11DOI: 10.1007/s12064-020-00336-0
Xin Zhang
Topological explanations in biology have been largely assumed to be free of mechanisms. However, by examining two classic topological explanations in the philosophical literature, this article has identified mechanisms in the corrected and complete formulations of both explanations. This constitutes the major work of this article. The minor work of this article is to address a follow-up question: given that these two topological explanations contain mechanisms, would this significantly blur the widely assumed boundary between topological and mechanistic explanations? My answer to this question is negative and the argument I have developed is that although these two topological explanations contain mechanisms, these mechanisms are explanatorily irrelevant to the target properties, which is in stark contrast to the situation in mechanistic explanations.
{"title":"Are topological explanations really free of mechanisms?","authors":"Xin Zhang","doi":"10.1007/s12064-020-00336-0","DOIUrl":"https://doi.org/10.1007/s12064-020-00336-0","url":null,"abstract":"<p><p>Topological explanations in biology have been largely assumed to be free of mechanisms. However, by examining two classic topological explanations in the philosophical literature, this article has identified mechanisms in the corrected and complete formulations of both explanations. This constitutes the major work of this article. The minor work of this article is to address a follow-up question: given that these two topological explanations contain mechanisms, would this significantly blur the widely assumed boundary between topological and mechanistic explanations? My answer to this question is negative and the argument I have developed is that although these two topological explanations contain mechanisms, these mechanisms are explanatorily irrelevant to the target properties, which is in stark contrast to the situation in mechanistic explanations.</p>","PeriodicalId":54428,"journal":{"name":"Theory in Biosciences","volume":"140 1","pages":"97-105"},"PeriodicalIF":1.1,"publicationDate":"2021-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12064-020-00336-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38805686","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-02-01Epub Date: 2020-10-13DOI: 10.1007/s12064-020-00322-6
Alexander Fürst von Lieven, Marcel Humar, Gerhard Scholtz
The Anatomai, a lost work written by Aristotle, must have contained a collection of various drawings and figures of species as well as their organs. In his texts (mainly the Historia animalium), Aristotle is often referring to the drawings after the description of species. Our study applies the method of the comparative view ('Vergleichendes Sehen') to provide an access to and reconstruction of Aristotle's lost illustrations based on his textual descriptions. As an example, we chose the treatment of the European lobster (Homarus gammarus L., 1758) in the Aristotelian corpus as a case study. First, we analyse the etymology of the Greek term astakós referring to the lobster and provide an overview on the putative synonyms. Second, we confront the textual basis of the description with several questions concerning the degree of abstraction, the relation between text and image, and the spatial orientation of the image. Finally, we present a step-by-step reconstruction of Aristotle's illustrations of the lobster based on the various passages dealing with its anatomy in the text of the Historia animalium. The problems which arise by a confrontation of the textual basis with hypothetical images are discussed at a more general level. We conclude that this kind of a text-based image reconstruction is only possible if the object described by Aristotle is unambiguously identifiable and still visually accessible.
{"title":"Aristotle's lobster: the image in the text.","authors":"Alexander Fürst von Lieven, Marcel Humar, Gerhard Scholtz","doi":"10.1007/s12064-020-00322-6","DOIUrl":"https://doi.org/10.1007/s12064-020-00322-6","url":null,"abstract":"<p><p>The Anatomai, a lost work written by Aristotle, must have contained a collection of various drawings and figures of species as well as their organs. In his texts (mainly the Historia animalium), Aristotle is often referring to the drawings after the description of species. Our study applies the method of the comparative view ('Vergleichendes Sehen') to provide an access to and reconstruction of Aristotle's lost illustrations based on his textual descriptions. As an example, we chose the treatment of the European lobster (Homarus gammarus L., 1758) in the Aristotelian corpus as a case study. First, we analyse the etymology of the Greek term astakós referring to the lobster and provide an overview on the putative synonyms. Second, we confront the textual basis of the description with several questions concerning the degree of abstraction, the relation between text and image, and the spatial orientation of the image. Finally, we present a step-by-step reconstruction of Aristotle's illustrations of the lobster based on the various passages dealing with its anatomy in the text of the Historia animalium. The problems which arise by a confrontation of the textual basis with hypothetical images are discussed at a more general level. We conclude that this kind of a text-based image reconstruction is only possible if the object described by Aristotle is unambiguously identifiable and still visually accessible.</p>","PeriodicalId":54428,"journal":{"name":"Theory in Biosciences","volume":"140 1","pages":"1-15"},"PeriodicalIF":1.1,"publicationDate":"2021-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12064-020-00322-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38481662","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-01-01DOI: 10.25163/biosciences.312000
John A Catanazaro, Gregor Mendel, Albrecht Kossel, Walter Sutton, Theodor Boveri. Phoebus Levene, Erwin Chargaff, John Catanzaro
In this review, a brief discussion of peptides, polypeptides, and their self-assembly architecture as a diverse platform for precision and personalized medicine. Self-assembly is a vital force of nature. The self-assembly process of the peptide chains is dynamic — reassembly repeatedly occurs in a self-healing manner. The interactions that happen to reassemble peptide structures include van der Waals forces, ionic bonds, hydrogen bonds, and hydrophobic forces. These forces also facilitate the molecular recognition function that the peptides encompass.
{"title":"The Power of Peptides: The Precision Molecules of Life","authors":"John A Catanazaro, Gregor Mendel, Albrecht Kossel, Walter Sutton, Theodor Boveri. Phoebus Levene, Erwin Chargaff, John Catanzaro","doi":"10.25163/biosciences.312000","DOIUrl":"https://doi.org/10.25163/biosciences.312000","url":null,"abstract":"In this review, a brief discussion of peptides, polypeptides, and their self-assembly architecture as a diverse platform for precision and personalized medicine. Self-assembly is a vital force of nature. The self-assembly process of the peptide chains is dynamic — reassembly repeatedly occurs in a self-healing manner. The interactions that happen to reassemble peptide structures include van der Waals forces, ionic bonds, hydrogen bonds, and hydrophobic forces. These forces also facilitate the molecular recognition function that the peptides encompass.","PeriodicalId":54428,"journal":{"name":"Theory in Biosciences","volume":"2 1","pages":""},"PeriodicalIF":1.1,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82088877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-12-01Epub Date: 2020-12-02DOI: 10.1007/s12064-020-00332-4
Nihat Ay
A core property of robust systems is given by the invariance of their function against the removal of some of their structural components. This intuition has been formalised in the context of input-output maps, thereby introducing the notion of exclusion independence. We review work on how this formalisation allows us to derive characterisation theorems that provide a basis for the design of robust systems.
{"title":"Ingredients for robustness.","authors":"Nihat Ay","doi":"10.1007/s12064-020-00332-4","DOIUrl":"https://doi.org/10.1007/s12064-020-00332-4","url":null,"abstract":"<p><p>A core property of robust systems is given by the invariance of their function against the removal of some of their structural components. This intuition has been formalised in the context of input-output maps, thereby introducing the notion of exclusion independence. We review work on how this formalisation allows us to derive characterisation theorems that provide a basis for the design of robust systems.</p>","PeriodicalId":54428,"journal":{"name":"Theory in Biosciences","volume":"139 4","pages":"309-318"},"PeriodicalIF":1.1,"publicationDate":"2020-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12064-020-00332-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38662279","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-12-01Epub Date: 2020-11-25DOI: 10.1007/s12064-020-00333-3
Deryc T Painter, Frank van der Wouden, Manfred D Laubichler, Hyejin Youn
To what extent do simultaneous innovations occur and are independently from each other? In this paper we use a novel persistent keyword framework to systematically identify innovations in a large corpus containing academic papers in evolutionary medicine between 2007 and 2011. We examine whether innovative papers occurring simultaneously are independent from each other by evaluating the citation and co-authorship information gathered from the corpus metadata. We find that 19 out of 22 simultaneous innovative papers do, in fact, occur independently from each other. In particular, co-authors of simultaneous innovative papers are no more geographically concentrated than the co-authors of similar non-innovative papers in the field. Our result suggests producing innovative work draws from a collective knowledge pool, rather than from knowledge circulating in distinct localized collaboration networks. Therefore, new ideas can appear at multiple locations and with geographically dispersed co-authorship networks. Our findings support the perspective that simultaneous innovations are the outcome of collective behavior.
{"title":"Quantifying simultaneous innovations in evolutionary medicine.","authors":"Deryc T Painter, Frank van der Wouden, Manfred D Laubichler, Hyejin Youn","doi":"10.1007/s12064-020-00333-3","DOIUrl":"10.1007/s12064-020-00333-3","url":null,"abstract":"<p><p>To what extent do simultaneous innovations occur and are independently from each other? In this paper we use a novel persistent keyword framework to systematically identify innovations in a large corpus containing academic papers in evolutionary medicine between 2007 and 2011. We examine whether innovative papers occurring simultaneously are independent from each other by evaluating the citation and co-authorship information gathered from the corpus metadata. We find that 19 out of 22 simultaneous innovative papers do, in fact, occur independently from each other. In particular, co-authors of simultaneous innovative papers are no more geographically concentrated than the co-authors of similar non-innovative papers in the field. Our result suggests producing innovative work draws from a collective knowledge pool, rather than from knowledge circulating in distinct localized collaboration networks. Therefore, new ideas can appear at multiple locations and with geographically dispersed co-authorship networks. Our findings support the perspective that simultaneous innovations are the outcome of collective behavior.</p>","PeriodicalId":54428,"journal":{"name":"Theory in Biosciences","volume":"139 4","pages":"319-335"},"PeriodicalIF":1.3,"publicationDate":"2020-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719117/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38304463","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-12-01Epub Date: 2020-11-19DOI: 10.1007/s12064-020-00327-1
Jürgen Jost
In computer science, we can theoretically neatly separate transmission and processing of information, hardware and software, and programs and their inputs. This is much more intricate in biology. Nevertheless, I argue that Shannon's concept of information is useful in biology, although its application is not as straightforward as many people think. In fact, the recently developed theory of information decomposition can shed much light on the complementarity between coding and regulatory, or internal and environmental information. The key challenge that we formulate in this contribution is to understand how genetic information and external factors combine to create an organism, and conversely how the genome has learned in the course of evolution how to harness the environment, and analogously how coding, regulation and spatial organization interact in cellular processes.
{"title":"Biological information.","authors":"Jürgen Jost","doi":"10.1007/s12064-020-00327-1","DOIUrl":"https://doi.org/10.1007/s12064-020-00327-1","url":null,"abstract":"<p><p>In computer science, we can theoretically neatly separate transmission and processing of information, hardware and software, and programs and their inputs. This is much more intricate in biology. Nevertheless, I argue that Shannon's concept of information is useful in biology, although its application is not as straightforward as many people think. In fact, the recently developed theory of information decomposition can shed much light on the complementarity between coding and regulatory, or internal and environmental information. The key challenge that we formulate in this contribution is to understand how genetic information and external factors combine to create an organism, and conversely how the genome has learned in the course of evolution how to harness the environment, and analogously how coding, regulation and spatial organization interact in cellular processes.</p>","PeriodicalId":54428,"journal":{"name":"Theory in Biosciences","volume":"139 4","pages":"361-370"},"PeriodicalIF":1.1,"publicationDate":"2020-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12064-020-00327-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38620017","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}