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Been Possible to Relate the Human Characteristics of the Hybrid Phenotype to the Number of Human Chromosomes Retained
HUMAN-MOUSE HYBRID CELL LINES CONTAINING PARTIAL COMPLEMENTS OF HUMAN CHROMOSOMES AND FUNCTIONING HUMA N GENES* BY MARY C. WEISSt AND HOWARD GREEN DEPARTMENT OF PATHOLOGY, NEW YORK UNIVERSITY SCHOOL OF MEDICINE Communicated by Boris Ephrussi, June 26, 1967 This paper will describe the isolation and properties of a group of new somatic hybrid cell lines obtained by crossing human diploid fibroblasts with an established mouse fibroblast line. These hybrids represent a combination between species more remote than those previously described (see, however, discussion of virus- induced heterokaryons). They are also the first reported hybrid cell lines con- taining human components and possess properties which may be useful for certain types of genetic investigations. Interspecific hybridizations involving rat-mouse,' hamster-mouse,2 3 and Ar- menian hamster-Syrian hamster4 combinations have been shown to yield popula- tions of hybrid cells capable of indefinite serial propagation. Investigations of the karyotype and phenotype of such hybrids have shown that both parental genomes are present2 5 and functional.6 In every case, some loss of chromosomes has been observed; this occurred primarily during the first few months of propagation, usually amounted to approximately 10-20 per cent of the complement present in newly formed hybrid cells, and involved chromosomes of both parents. Recent studies have provided evidence of preferential loss of chromosomes of one parental species in interspecific hybrids.2'5 A more extreme example of this preferential loss has been encountered in the human-mouse hybrid lines to be described, in which at least 75 per cent, and in some cases more than 95 per cent, of the human complement has been lost. -
A Giant of Genetics Cornell University As a Graduate Student to Work on the Cytogenetics of George Beadle, an Uncommon Maize
BOOK REVIEW farm after obtaining his baccalaureate at Nebraska Ag, he went to A giant of genetics Cornell University as a graduate student to work on the cytogenetics of George Beadle, An Uncommon maize. On receiving his Ph.D. from Cornell in 1931, Beadle was awarded a National Research Council fellowship to do postdoctoral work in T. H. Farmer: The Emergence of Genetics th Morgan’s Division of Biology at Caltech, where the fruit fly, Drosophila, in the 20 Century was then being developed as the premier experimental object of van- By Paul Berg & Maxine Singer guard genetics. On encountering Boris Ephrussi—a visiting geneticist from Paris— Cold Spring Harbor Laboratory Press, at Caltech, Beadle began his work on the mechanism of gene action. 2003 383 pp. hardcover, $35, He and Ephrussi studied certain mutants of Drosophila whose eye ISBN 0-87969-688-5 color differed in various ways from the red hue characteristic of the wild-type fly. They inferred from these results that the embryonic Reviewed by Gunther S Stent development of animals consists of a series of chemical reactions, each step of which is catalyzed by a specific enzyme, whose formation is, in http://www.nature.com/naturegenetics turn, controlled by a specific gene. This inference provided the germ for Beadle’s one-gene-one-enzyme doctrine. To Beadle and Ephrussi’s “Isaac Newton’s famous phrase reminds us that major advances in disappointment, however, a group of German biochemists beat them science are made ‘on the shoulders of giants’. Too often, however, the to the identification of the actual chemical intermediates in the ‘giants’ in our field are unknown to many colleagues and biosynthesis of the Drosophila eye color pigments. -
905 Crossovers Between Epigenesis and Epigenetics
MEDICINA NEI SECOLI ARTE E SCIENZA, 26/3 (2014) 905-942 Journal of History of Medicine Articoli/Articles CROSSOVERS BETWEEN EPIGENESIS AND EPIGENETICS. A MULTICENTER APPROACH TO THE HISTORY OF EPIGENETICS (1901-1975) ROSSELLA COSTA AND GIULIA FREZZA Dipartimento di Scienze e Biotecnologie Medico-Chirurgiche, Sapienza, Università di Roma, I SUMMARY The origin of epigenetics has been traditionally traced back to Conrad Hal Waddington’s foundational work in 1940s. The aim of the present paper is to reveal a hidden history of epigenetics, by means of a multicenter approach. Our analysis shows that genetics and embryology in early XX century – far from being non-communicating vessels – shared similar questions, as epitomized by Thomas Hunt Morgan’s works. Such questions were rooted in the theory of epigenesis and set the scene for the development of epigenetics. Since the 1950s, the contribution of key scientists (Mary Lyon and Eduardo Scarano), as well as the discussions at the international conference of Gif-sur-Yvette (1957) paved the way for three fundamental shifts of focus: 1. From the whole embryo to the gene; 2. From the gene to the complex extranuclear processes of development; 3. From cytoplasmic inheritance to the epigenetics mechanisms. Introduction Mainstream literature considers the British scientist Conrad Hal Waddington’s pioneering insights, at the crossroad of embryological and genetic studies, the first attempt to create a coherent frame of epigenetics in the mid of XX century1. Recently, a second parallel origin, referred to the American ciliatologist David Nanney, mainly Key words: Epigenesis - Epigenetics - T.H. Morgan - E. Scarano - Methylation. 905 Rossella Costa and Giulia Frezza focusing on cell differentiation, has been put in evidence2. -
Be Convenient, It Can Be Only Tentative for It Is Not Demonstrated That These Correspond with Different Genetical Types
REVIEWS TREASURYOF HUMAN INHERITANCE. Vol. V. Part II. On syndactyly and its association with polydactyly. By Julia Bell. Cambridge University Press. 1953. lOs. 6d. Thisis the latest addition to the valuable collection of human pedigrees featuring pathological and abnormal conditions which during some forty years have been brought together in the Treasury of Human Inheritance under the sponsorship of the Galton Laboratory. From an exhaustive study of the genetical and medical literature, Dr Bell has assembled 63 pedigrees which include some 700 predominantly syndactylous digital anomalies. The varied manifestation of syndactyly, the association with polydactyly, differences in its sex incidence and the difficult problem of its inheritance, these are questions considered in a preliminary note. The genetical analysis of this material would certainly be of great interest. Dr Bell has classified the pedigrees on the basis of the varied manifestation and whilst this may be convenient, it can be only tentative for it is not demonstrated that these correspond with different genetical types. However, it does focus attention on interesting sex differences in the incidence of the various forms of this defect. Noteworthy amongst the collection is Schofield's unique pedigree (fig. 125) in which webbed toes are limited to males, being transmitted only from father to son, completely in accordance with the inheritance of a single gene on the Y-chromosome. One normal sister has been lost from this pedigree in transcription. J. H. BENNETT. NUCLEO-CYTOPLASMICRELATIONS IN MICRO-ORGANISMS. Their bearing on cell heredity and differentiation. By Boris Ephrussi. Oxford : Geoffrey Cumberlege, Clarendon Press. 1953. Pp. 127. 18s. -
The Hereditary Statistics of Hugo De Vries
Acta Bot. Neerl. 47(4), December 1998, p. 427—463 The Hereditary Statistics of Hugo de Vries Erik Zevenhuizen Institute for Systematics and Population Biology, Faculty of Biology, University of Amsterdam, Kruislaan 318, 1098 SM Amsterdam, The Netherlands CONTENTS Introduction 427 The theory of pangenesis 429 The use of statistics 432 The laws of chance 435 The Veronica-note: the 5/16-law 439 The Veronica-note: the 1.2.1-law 446 The Aster-note 449 Conclusion: in search of the laws of nature 452 Keywords: Hugo de Vries, Mendel’s laws, mutation theory, pangenesis. INTRODUCTION de Vries is remembered the first of three botanists in Today, Hugo chiefly as who, 1900, publicly announced that they had discovered what we now call the laws of Mendel. All three maintainedthat they had foundthe laws on their own and that, at the moment they did their discovery, they had been completely unaware of the fact that the Austrian amateur botanist Gregor Mendel (1822-1884) had published similar conclusions already in 1866. Whereas his contributions to the development of evolutionary thought are De Vries is credited in generally unappreciated or simply unknown, many surveys on the history of genetics for his rediscovery of Mendel’s laws. It is generally accepted that, together with his two fellow-rediscoverers, Carl Correns from Tubingen and Erich von Tschermak-Seysenegg from Vienna, De Vries made these basic rules of genetics scientific widely known to the world. The year 1900 can be considered as the year of birth of modern genetics, and Hugo de Vries as one of the founders of the discipline. -
Darwin's Influence on Mendel: Evidence from a New Translation Of
| PERSPECTIVES Darwin’sInfluence on Mendel: Evidence from a New Translation of Mendel’s Paper Daniel J. Fairbanks*,1 and Scott Abbott† *Department of Biology and †Department of Integrated Studies, Utah Valley University, Orem, Utah 84058 ORCID ID: 0000-0001-7422-0549 (D.J.F.) ABSTRACT Gregor Mendel’s classic paper, Versuche über Pflanzen-Hybriden (Experiments on Plant Hybrids), was published in 1866, hence 2016 is its sesquicentennial. Mendel completed his experiments in 1863 and shortly thereafter began compiling the results and writing his paper, which he presented in meetings of the Natural Science Society in Brünn in February and March of 1865. Mendel owned a personal copy of Darwin’s Origin of Species, a German translation published in 1863, and it contains his marginalia. Its publication date indicates that Mendel’s study of Darwin’s book could have had no influence while he was conducting his experiments but its publication date coincided with the period of time when he was preparing his paper, making it possible that Darwin’s writings influenced Mendel’s interpretations and theory. Based on this premise, we prepared a Darwinized English translation of Mendel’s paper by comparing German terms Mendel employed with the same terms in the German translation of Origin of Species in his possession, then using Darwin’s counterpart English words and phrases as much as possible in our translation. We found a substantially higher use of these terms in the final two (10th and 11th) sections of Mendel’s paper, particularly in one key paragraph, where Mendel reflects on evolutionary issues, providing strong evidence of Darwin’sinfluence on Mendel. -
"Neutral 'Petites'" and "Suppressive 'Petites'" (The One Previously Studied6 Belonging to the Former Class).6
SUPPRESSIVENESS: A NEW FACTOR IN THE GENETIC DETERMINISM OF THE SYNTHESIS OF RESPIRATORY ENZYMES IN YEAST BY BORIS EPHRUSSI, HtLE'NE DE MARGERIE-HOTTINGUER, AND HERSCHEL ROMAN* LABORATOIRE DE GANATIQUE PHYSIOLOGIQUE, CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE, PARIS, FRANCE Communicated by G. W. Beadle, September 27, 1955 In a series of papers from this laboratory' published since 1949, it was shown that clones of baker's yeast (Saccharomyces cerevisiae), whether diploid or haploid, con- stantly give rise during their growth to mutants ("vegetative 'petites' ") which are stable in vegetative reproduction and are characterized by a reduced colony size on media in which sugar is the limiting factor. The reduced colony size was shown to be due to a respiratory deficiency of the mutant cells,2 due in turn to the lack of several enzymes (including cytochrome oxidase) bound, in normal yeast, to par- ticles sedimentable by centrifugation.' It was suggested that, from the genetical point of view, the mutation resulting in the production of vegetative mutants con- sists in the loss or irreversible functional inactivation of a particulate cytoplasmic autoreproducing factor, required for the synthesis of respiratory enzymes.4 This interpretation was based on the results of crosses which will be recalled below. It will suffice to say at this point that a single strain of vegetative mutants was utilized in the earlier detailed genetic study;5 thus, until more recently, no systematic at- tempts had been made to compare the genetic behavior of a number of such mutants of independent origin. It is such a study, undertaken three years ago, that has now revealed that there exist at least two types of vegetative respiratory mutants which are, so far as we know, identical biochemically but which can be distinguished by their behavior in crosses with normal yeast. -
Fate of Mitochondrial DNA in Human-Mouse Somatic Cell Hybrids (Density Gradient Centrifugation/Ethidium Bromide/Karyotype)
Proc. Nat. Acad. Sci. USA Vol. 69, No. 1, pp. 129-133, January 1972 Fate of Mitochondrial DNA in Human-Mouse Somatic Cell Hybrids (density gradient centrifugation/ethidium bromide/karyotype) BARBARA ATTARDI* AND GIUSEPPE ATTARDI* Centre de Gen6tique Molculaire, 91 Gif-sur-Yvette, France Communicated by Boris Ephrussi, November 3, 1971 ABSTRACT Several hybrid lines between human and In the present work, the fate of parental mit-DNA was mouse somatic cells, containing one or two complements of mouse chromosomes and a reduced complement of human investigated in several human-mouse hybrid cell lines. For chromosomes, have been examined for the presence of this analysis, advantage was taken of the possibility of re- mouse and human mitochondrial DNAs. For this analysis, solving mouse and human mit-DNAs on the basis of their advantage was taken of the fact that these two types of difference in buoyant density in CsCl gradients. Only mitochondrial DNA have a buoyant density difference in mouse-type mit-DNA was detected in all hybrid clones CsCl gradients of 0.008 g/cm'. In all the hybrid clones analyzed, which retained an average number of human examined, even in hybrids estimated conservatively to con- chromosomes estimated conservatively to vary from 5 tain an average of at least 23 residual human chromosomes to 23, only mitochondrial DNA of mouse character was per cell. detected. It seems likely that either repression of relevant human genes by the mouse genome or loss of human MATERIALS AND METHODS chromosomes is responsible for these results. If the latter explanation is true, since chromosome loss under the Cells and Media. -
Tutorial: Mendelian Genetics
Mendelian Genetics Contents Introduction ........................................................................................................................ 1 Heredity Before Mendel ..................................................................................................... 2 Mendel and the Laws of Heredity....................................................................................... 4 The “Rediscovery” of Mendel ............................................................................................. 7 The Misuse of Mendel ........................................................................................................ 8 Mendel in the Modern World ........................................................................................... 10 References and Resources ................................................................................................ 10 Supplemental Material ..................................................................................................... 11 Introduction Today, when the word “genetics” is mentioned the mind is at once occupied with terms like cloning, PCR, the genome project, and genomics. Just a few decades ago, however, the word genetics conjured up a very different set of terms including crossing, segregation, Punnett square, and binomial expansion. It is not that these terms have disappeared or have been replaced since, it is, rather, that genetics moved full force into the molecular era in the late 1970s and, in the beginning of the twenty-first century, -
The Singular Fate of Genetics in the History of French Biology, 1900-1940 Richard Burian, Jean Gayon, Doris Zallen
The singular fate of Genetics in the History of French Biology, 1900-1940 Richard Burian, Jean Gayon, Doris Zallen To cite this version: Richard Burian, Jean Gayon, Doris Zallen. The singular fate of Genetics in the History of French Biology, 1900-1940. Journal of the History of Biology, Springer Verlag, 1988, 21 (3), pp.357-402. 10.1007/BF00144087. halshs-00775435 HAL Id: halshs-00775435 https://halshs.archives-ouvertes.fr/halshs-00775435 Submitted on 16 Apr 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. The Singular Fate of Genetics in the History of French Biology, 1900-l 940 RICHARD M. BURIAN” Department of Philosophy Virginia Polytechnic Institute and State University Blacksburg, Virginia 24601 JEAN GAYON Faculti de lettres etphilosophie Universite’ de Bourgogne DQon, France DORIS ZALLEN Center for Programs in the Humanities Virginia Polytechnic Institute and State Universily Blacksburg, Virginia 24601 INTRODUCTION It has often been remarked how long it took genetics to penetrate French science. This observation is just. It was not until the late 1940s for example, that genetics appeared in an official university curriculum. At the same time, it is also well known that, as early as the 1940s, French scientists played an important role at the forefront of genetic research, specifically in work that helped bring about the transition to molecular genetics. -
The Full Breadth of Mendel's Genetics
| PERSPECTIVES The Full Breadth of Mendel’s Genetics Peter J. van Dijk*,1 and T. H. Noel Ellis *Keygene N.V., 6708 PW Wageningen, The Netherlands ABSTRACT Gregor Mendel’s “Experiments on Plant Hybrids” (1865/1866), published 150 years ago, is without doubt one of the most brilliant works in biology. Curiously, Mendel’s later studies on Hieracium (hawkweed) are usually seen as a frustrating failure, because it is assumed that they were intended to confirm the segregation ratios he found in Pisum. Had this been his intention, such a confirmation would have failed, since, unknown to Mendel, Hieracium species mostly reproduce by means of clonal seeds (apomixis). Here we show that this assumption arises from a misunderstanding that could be explained by a missing page in Mendel’s first letter to Carl Nägeli. Mendel’s writings clearly indicate his interest in “constant hybrids,” hybrids which do not segregate, and which were “essentially different” from “variable hybrids” such as in Pisum.AfterthePisum studies, Mendel worked mainly on Hieracium for 7 years where he found constant hybrids and some great surprises. He also continued to explore variable hybrids; both variable and constant hybrids were of interest to Mendel with respect to inheritance and to species evolution. Mendel considered that their similarities and differences might provide deep insights and that their differing behaviors were “individual manifestations of a higher more fundamental law.” KEYWORDS Gregor Mendel; genetics; Hieracium; constant hybrids; apomixis The publication of Mendel’s letters to Carl Nägeli by several fertile hybrids will bloom for the first time. They Correns in 1905 was a service to genetics which seems not should be very numerous and I only hope that they repay to have been fully appreciated by most of those who have since the yearning [Sehnsucht!] with which I await them with ’ written accounts of Mendel slifeandwork(MannLesley much information concerning their life histories.” (quoted 1927). -
Monod and the Spirit of Molecular Biology Michel Morange
Monod and the spirit of molecular biology Michel Morange To cite this version: Michel Morange. Monod and the spirit of molecular biology. Comptes Rendus Biologies, Elsevier Masson, 2015. hal-01359097 HAL Id: hal-01359097 https://hal.archives-ouvertes.fr/hal-01359097 Submitted on 1 Sep 2016 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution - NonCommercial - NoDerivatives| 4.0 International License Titre : Monod, et l’esprit de la biologie moléculaire Title: Monod and the spirit of molecular biology Auteur : Michel Morange USR3608 Centre Cavaillès – République des Savoirs École normale supérieure 29, rue d’Ulm F-75230 Paris Cedex 5 Tél. : +33 (0)1 44 32 29 61 Courriel : [email protected] Résumé : Les fondateurs de la biologie moléculaire partageaient certaines vues sur la place de la biologie parmi les sciences, aussi bien que sur les relations de la biologie moléculaire avec le darwinisme. Monod ne faisait pas exception, mais l’étude de ses écrits est particulièrement intéressante car il exprime son point de vue avec une grande clarté, et pousse les conséquences de ses choix plus loin que la plupart de ses contemporains.