LA PATRAÑA IZQUIERDISTA DEL “GEN ROJO”:
DESMENTIDO DE “EL GEN ROJO” Y REHABILITACION DEL DOCTOR VALLEJO NAGERA Y LOBON:
xtracto de mi biografía del Excelentísimo e Ilustrísimo Señor Usía el Caballero Don Antonio José Vallejo Nágera y Lobón:
¡El “gen rojo” no ha sido jamás expresión del Doctor Vallejo Nágera y Lobón, ni de ningún psiquiatra, ni empleado sanitario de su equipo de investigación y Ciencias! ¡Ni siquoera exostía en 1938-39 esa palabra, ni término técnico, vonsagrado en la Ciencia biológica nucho después, con la creación de la Genética como disciplina científicoempírica de Biología (zoología y botánica). Las investigaciones del Gabinete y de El Gran Lobo no eran genéticas propiamente dichas, ni de análisos biológico estricto mendeliano de la herencia racial biológica puramente somática, ni corporal y psicológicoempírica. Se estudiaba a los especímenes en cuanto a su calidad “in actu” fenotípica” y estado de salud mental, von características esenciales de lo que ordinariamente se denominaba “la raza” y que, en este caso, se refería a las razas y a la sociedad con características raciales reconocibles, sea que se tratase de especímenes racial y presuntamente puros, sea que fuesen híbridos, o razas derivadas. Pero el objeto formal del estudio del Gabinete no era, o no lo fue todavía, y lo hubiera podido ser, si hubiese contado con idea y vomuntad política, más medios y más tiempo, identificar y seleccionar razas y especímenes, para la creación de una Nueva España con un nuevo Orden Racial y meta de los anhelos del linajismo, racismo y aristocraticismo de Sangre y herencial del Integrismo de Limpieza de Sangre más agudo y perfecto. Tampoco se trataba de probar que el marxismo leninismo es, por esencia y definición, una enfermedad psíquica, una patología médica general, o específica. no eran psiquiatras incultos o “con oregeras”, sabían que el marxismo leninismo es doctrina espiritual y, por añadidura, sentimental: es básicamente de índole intelectual, filosófica, de Filosofía Política, con expresión somera y rudimentaria de sus principios metafísicos ontológicos, pero con abundante capital desarrollo doctrinal político y de estrategia y táctica políticas, de arte teórico político con consiguientes interpretaciones y apreciaciones sobre los regímenes políticoss y ensayos sobre la Historia económica de pueblos de la Humanidad. Lógicamente los criminales y bestiales lerdos frentepopulistas presos estudiados no eran ideólogos, puefe que ni siquiera conocieran lo más elemental ortodoxo del verdadero marxismo leninismo, pero eran parcialmente producto fenoménico de esa cosmovisión judía perversa “in spiritu”, para no judíos y para embrutecer y dominar a éstos en todo el mundo. Algo típico del comunisno marxista tenían: la principal o más alta estima por “parias”, “proletariado” masificado e industrializado, o plebe asalariada y pobre, y la chusma con sus ideales de vida subpuerca. La finalidad oficial, real, institucional, profesional, científica y política del Gabinete, culto en Humanidades, no era siquiera afirmar que el marxismo es algo material, puramente cerebral, psiquiátrico anímico, ni patología propiamente dicha espiritual, sino perversión espiritual filosófica, metafísica, especulativa (en sentodo técnico escolástico) y ética; ahora bien, era y es, eso sí: un fenómeno mental ASOCIADO A PATOLOGIAS PSIQUIATRICAS, PROMOTOR DE ALGUNA O ALGUNAS, O / E INCLUSO EFECTO PARCIAL DE ALGUNA O ALGUNAS ENFERMEDADES PSIQUIÁTRICAS
NADA DE BUSQUEDA DE GEN ROJO NI DE SU “PURA” MADRE. NADA DE MARXISMO CUAL ENFERMEDAD PURAMENTE CEREBRAL, SOMÁTICA, PSICOSOMÁTICA, O PSIQUIATRICA, SINO FENOMENO ORA CAUSA, ORA EFECTO, ORA AMBOS, DE UNA O MAS PATOLOGÍAS MENTALES, NORMAL Y ESTADISTICAMENTE.
El concepto de gen (gen molecular) es definido con la realidad tardíamente descubierta a que se refiere en Ciencia empírica que concreta, con nuevo descubrimiento empírico, el significado del término “gen”, dámdole uno nuevo específico, en 1953, año del descubrimiento de la estructura helicoloidal del ADN, e inicio de la Genética específica hodierna, como Biología molecular de la herencia y química/física del engendraniento y reproducción de los seres vivos. Anteriorente se concebía al gen como una cadena de proteinas, sin aplicación o desarrollo técnicos genésicoherenciales o raciales*.
*El gemano Wilhem Hofmeister descubió empíricamente elcromosoma en 1848, y la palabra gen (sin significado posterior progresado de biología molecular específicamente precisa en 1953, con el descubrimiento de la estructura helicoidad de cromosima, en el nuevo concento rspecífico que ha heredado el primitivo nombre de gen) es creada en 1909 por el danés Wilhelm Johannsen, si bien los conocimientos de los genomas y las posibilidades de manipulación genética intracelular comienzan a finales del siglo XX, en interrelación con la nanotecnología [término del japonés Norio Taniguchi en 1974], la cuál empieza a prosperar con amplias posibilidades desde 1991 [cf.https://naukas.com/2014/01/13/el-descubrimiento-de-los-nanotubos-de-carbono/ ]
He aquí el texto original del artículo de los científicos biólogos James Dewey Watson (Chicago, 6 de Abril de 1928) y Francis Harry Compton Crick, (8 de junio de 1916 – 28 de julio de 2004), publicado en el número de la revista científica “Nature“, el 25 de Abril de 1953, con anotaciones ulteriores de ambos autores:
April 25, 1953 (2), Nature (3
|Back||Print this page
If the link above doesn’t work, try typing Ctrl + P on a PC or Apple + P on a Macintosh.
|reprinted with permission from Nature magazine
A Structure for Deoxyribose Nucleic Acid
April 25, 1953 (2), Nature (3), 171, 737-738
We wish to suggest a structure for the salt of deoxyribose nucleic acid (D.N.A.). This structure has novel features which are of considerable biological interest.
A structure for nucleic acid has already been proposed by Pauling (4)and Corey1. They kindly made their manuscript available to us in advance of publication. Their model consists of three intertwined chains, with the phosphates near the fibre axis, and the bases on the outside. In our opinion, this structure is unsatisfactory for two reasons:
(1) We believe that the material which gives the X-ray diagrams is the salt, not the free acid. Without the acidic hydrogen atoms it is not clear what forces would hold the structure together, especially as the negatively charged phosphates near the axis will repel each other.
(2) Some of the van der Waals distances appear to be too small.
Another three-chain structure has also been suggested by Fraser (in the press). In his model the phosphates are on the outside and the bases on the inside, linked together by hydrogen bonds. This structure as described is rather ill-defined, and for this reason we shall not comment on it.
The structure is an open one, and its water content is rather high. At lower water contents we would expect the bases to tilt so that the structure could become more compact.
The novel feature of the structure is the manner in which the two chains are held together by the purine and pyrimidine bases. The planes of the bases are perpendicular to the fibre axis. They are joined together in pairs, a single base from one chain being hydroden-bonded to a single base from the other chain, so that the two lie side by side with identical z-coordinates. One of the pair must be a purine and the other a pyrimidine for bonding to occur. The hydrogen bonds are made as follows: purine position 1 to pyrimidine position 1; purine position 6 to pyrimidine position 6.
If it is assumed that the bases only occur in the structure in the most plausible tautomeric forms (that is, with the keto rather than the enol configurations) it is found that only specific pairs of bases can bond together. These pairs are: adenine (purine) with thymine (pyrimidine), and guanine (purine) with cytosine (pyrimidine) (9).
In other words, if an adenine forms one member of a pair, on either chain, then on these assumptions the other member must be thymine; similarly for guanine and cytosine. The sequence of bases on a single chain does not appear to be restricted in any way. However, if only specific pairs of bases can be formed, it follows that if the sequence of bases on one chain is given, then the sequence on the other chain is automatically determined.
It has been found experimentally3,4that the ratio of the amounts of adenine to thymine, and the ratio of guanine to cytosine, are always very close to unity for deoxyribose nucleic acid.
It is probably impossible to build this structure with a ribose sugar in place of the deoxyribose, as the extra oxygen atom would make too close a van der Waals contact.
The previously published X-ray data5,6on deoxyribose nucleic acid are insufficient for a rigorous test of our structure. So far as we can tell, it is roughly compatible with the experimental data, but it must be regarded as unproved until it has been checked against more exact results. Some of these are given in the following communications (10). We were not aware of the details of the results presented there when we devised our structure (11), which rests mainly though not entirely on published experimental data and stereochemical arguments.
It has not escaped our notice (12)that the specific pairing we have postulated immediately suggests a possible copying mechanism for the genetic material.
Full details of the structure, including the conditions assumed in building it, together with a set of coordinates for the atoms, will be published elsewhere (13).
We are much indebted to Dr. Jerry Donohue for constant advice and criticism, especially on interatomic distances. We have also been stimulated by a knowledge of the general nature of the unpublished experimental results and ideas of Dr. M. H. F. Wilkins, Dr. R. E. Franklin and their co-workers at King’s College, London. One of us (J. D. W.) has been aided by a fellowship from the National Foundation for Infantile Paralysis.
1 Pauling, L., and Corey, R. B., Nature, 171, 346 (1953); Proc. U.S. Nat. Acad. Sci., 39, 84 (1953).
Aware of these profound implications, Watson and Crick were obsessed with the problem—and, perhaps more than any other scientists, they were determined to find the answer first. Their competitive spirit drove them to work quickly, and it undoubtedly helped them succeed in their quest.
Watson and Crick’s rapport led them to speedy insights as well. They incessantly discussed the problem, bouncing ideas off one another. This was especially helpful because each one was inspired by different evidence. When the visually sensitive Watson, for example, saw a cross-shaped pattern of spots in an X-ray photograph of DNA, he knew DNA had to be a double helix. From data on the symmetry of DNA crystals, Crick, an expert in crystal structure, saw that DNA’s two chains run in opposite directions.
Since the groundbreaking double helix discovery in 1953, Watson has used the same fast, competitive approach to propel a revolution in molecular biology. As a professor at Harvard in the 1950s and 1960s, and as past director and current president of Cold Spring Harbor Laboratory, he tirelessly built intellectual arenas—groups of scientists and laboratories—to apply the knowledge gained from the double helix discovery to protein synthesis, the genetic code, and other fields of biological research. By relentlessly pushing these fields forward, he also advanced the view among biologists that solving major health problems requires research at the most fundamental level of life.
(2) On this date, Nature published the paper you are reading.
According to science historian Victor McElheny of the Massachusetts Institute of Technology, this date was a turning point in a longstanding struggle between two camps of biology, vitalism and reductionism. While vitalists studied whole organisms and viewed genetics as too complex to understand fully, reductionists saw deciphering fundamental life processes as entirely possible—and critical to curing human diseases. The discovery of DNA’s double-helix structure was a major blow to the vitalist approach and gave momentum to the reductionist field of molecular biology.
Historians wonder how the timing of the DNA race affected its outcome. Science, after years of being diverted to the war effort, was able to focus more on problems such as those affecting human health. Yet, in the United States, it was threatened by a curb on the free exchange of ideas. Some think that American researcher Linus Pauling would have beaten Watson and Crick to the punch if Pauling’s ability to travel had not been hampered in 1952 by the overzealous House Un-American Activities Committee.
(3) Nature (founded in 1869)——and hundreds of other scientific journals—help push science forward by providing a venue for researchers to publish and debate findings. Today, journals also validate the quality of this research through a rigorous evaluation called peer review. Generally at least two scientists, selected by the journal’s editors, judge the quality and originality of each paper, recommending whether or not it should be published.
Science publishing was a different game when Watson and Crick submitted this paper to Nature.With no formal review process at most journals, editors usually reached their own decisions on submissions, seeking advice informally only when they were unfamiliar with a subject.
(4) The effort to discover the structure of DNA was a race among several players. They were world-renowned chemist Linus Pauling at the California Institute of Technology, and X-ray crystallographers Maurice Wilkins and Rosalind Franklin at King’s College London, in addition to Watson and Crick at the Cavendish Laboratory, Cambridge University.
The competitive juices were flowing well before the DNA sprint was in full gear. In 1951, Pauling narrowly beat scientists at the Cavendish Lab, a top center for probing protein structure, to the discovery that certain proteins are helical. The defeat stung. When Pauling sent a paper to be published in early 1953 that proposed a three-stranded DNA structure, the head of the Cavendish gave Watson and Crick permission to work full-time on DNA’s structure. Cavendish was not about to lose twice to Pauling.
Pauling’s proposed structure of DNA was a three-stranded helix with the bases facing out. While the model was wrong, Watson and Crick were sure Pauling would soon learn his error, and they estimated that he was six weeks away from the right answer. Electrified by the urgency—and by the prospect of beating a science superstar—Watson and Crick discovered the double helix after a four-week frenzy of model building.
Pauling was foiled in his attempts to see X-ray photos of DNA from King’s College—crucial evidence that inspired Watson’s vision of the double helix—and had to settle for inferior older photographs. In 1952, Wilkins and the head of the King’s laboratory had denied Pauling’s request to view their photos. Pauling was planning to attend a science meeting in London, where he most likely would have renewed his request in person, but the United States House Un-American Activities Committee halted Pauling’s trip, citing his antiwar activism. It was fitting, then, that Pauling, who won the Nobel Prize in Chemistry in 1954, also won the Nobel Peace Prize in 1962, the same year Watson and Crick won their Nobel Prize for discovering the double helix.
(5) Here, the young scientists Watson and Crick call their model “radically different” to strongly set it apart from the model proposed by science powerhouse Linus Pauling. This claim was justified. While Pauling’s model was a triple helix with the bases sticking out, the Watson-Crick model was a double helix with the bases pointing in and forming pairs of adenine (A) with thymine (T), and cytosine (C) with guanine (G).
(6) This central description of the double helix model still stands today—a monumental feat considering that the vast majority of research findings are either rejected or changed over time.
According to science historian Victor McElheny of the Massachusetts Institute of Technology, the staying power of the double helix theory puts it in a class with Newton’s laws of motion. Just as Newtonian physics has survived centuries of scientific scrutiny to become the foundation for today’s space programs, the double helix model has provided the bedrock for several research fields since 1953, including the biochemistry of DNA replication, the cracking of the genetic code, genetic engineering, and the sequencing of the human genome.
(7) Norwegian scientist Sven Furberg’s DNA model—which correctly put the bases on the inside of a helix—was one of many ideas about DNA that helped Watson and Crick to infer the molecule’s structure. To some extent, they were synthesizers of these ideas. Doing little laboratory work, they gathered clues and advice from other experts to find the answer. Watson and Crick’s extraordinary scientific preparation, passion, and collaboration made them uniquely capable of this synthesis.
(8) A visual representation of Watson and Crick’s model was crucial to show how the components of DNA fit together in a double helix. In 1953, Crick’s wife, Odile, drew the diagram used to represent DNA in this paper. Scientists use many different kinds of visual representations of DNA.
(9) The last hurdle for Watson and Crick was to figure out how DNA’s four bases paired without distorting the helix. To visualize the answer, Watson built cardboard cutouts of the bases. Early one morning, as Watson moved the cutouts around on a tabletop, he found that only one combination of base molecules made a DNA structure without bulges or strains. As Crick put it in his book What Mad Pursuit, Watson solved the puzzle “not by logic but serendipity.” Watson and Crick picked up this model-building approach from eminent chemist Linus Pauling, who had successfully used it to discover that some proteins have a helical structure.
(10) Alongside the Watson-Crick paper in the April 25, 1953, issue of Nature were separately published papers by scientists Maurice Wilkins and Rosalind Franklin of King’s College, who worked independently of each other. The Wilkins and Franklin papers described the X-ray crystallography evidence that helped Watson and Crick devise their structure. The authors of the three papers, their lab chiefs, and the editors of Nature agreed that all three would be published in the same issue.
The “following communications” that our authors are referring to are the papers by Franklin and Wilkins, published on the journal pages immediately after Watson and Crick’s paper. They (and other papers) can be downloaded as PDF files (Adobe Acrobat required) from Nature’s 50 Years of DNA website (http://www.nature.com/nature/dna50/archive.html).
Here are the direct links:
Molecular Configuration in Sodium Thymonucleate
Molecular Structure of Deoxypentose Nucleic Acids
(11) This sentence marks what many consider to be an inexcusable failure to give proper credit to Rosalind Franklin, a King’s College scientist. Watson and Crick are saying here that they “were not aware of” Franklin’s unpublished data, yet Watson later admits in his book The Double Helixthat these data were critical in solving the problem. Watson and Crick knew these data would be published in the same April 25 issue of Nature,but they did not formally acknowledge her in their paper.
But Franklin was frustrated with an inhospitable environment at King’s, one that pitted her against her colleagues. And in an institution that barred women from the dining room and other social venues, she was denied access to the informal discourse that is essential to any scientist’s work. Seeing no chance for a tolerable professional life at King’s, Franklin decided to take another job. As she was preparing to leave, she turned her X-ray photographs over to her colleague Maurice Wilkins (a longtime friend of Crick).
Then, in perhaps the most pivotal moment in the search for DNA’s structure, Wilkins showed Watson one of Franklin’s photographs without Franklin’s permission. As Watson recalled, “The instant I saw the picture my mouth fell open and my pulse began to race.” To Watson, the cross-shaped pattern of spots in the photo meant that DNA had to be a double helix.
Was it unethical for Wilkins to reveal the photographs? Should Watson and Crick have recognized Franklin for her contribution to this paper? Why didn’t they? Would Watson and Crick have been able to make their discovery without Franklin’s data? For decades, scientists and historians have wrestled over these issues.
To read more about Rosalind Franklin and her history with Wilkins, Watson, and Crick, see the following:
“Light on a Dark Lady” by Anne Piper, a lifelong friend of Franklin’s
“The Double Helix and the Wronged Heroine,” an essay on Nature’s “Double Helix: 50 years of DNA” Web site
A review of Brenda Maddox’s recent book, Rosalind Franklin: The Dark Lady of DNA in The Guardian(UK)
(12) This phrase and the sentence it begins may be one of the biggest understatements in biology. Watson and Crick realized at the time that their work had important scientific implications beyond a “pretty structure.” In this statement, the authors are saying that the base pairing in DNA (adenine links to thymine and guanine to cytosine) provides the mechanism by which genetic information carried in the double helix can be precisely copied. Knowledge of this copying mechanism started a scientific revolution that would lead to, among other advances in molecular biology, the ability to manipulate DNA for genetic engineering and medical research, and to decode the human genome, along with those of the mouse, yeast, fruit fly, and other research organisms.
(13) This paper is short because it was intended only to announce Watson and Crick’s discovery, and because they were in a competitive situation. In January 1954, they published the “full details” of their work in a longer paper (in Proceedings of the Royal Society). This “expound later” approach was usual in science in the 1950s as it continues to be. In fact, Rosalind Franklin did the same thing, supplementing her short April 25 paper with two longer articles.
Today, scientists publish their results in a variety of formats. They also present their work at conferences. Watson reported his and Crick’s results at the prestigious annual symposium at Cold Spring Harbor Laboratory in June 1953. As part of our recognition of the fiftieth anniversary of the double helix discovery, we will join scientists at Cold Spring Harbor as they present their papers at the “Biology of DNA” conference.