ArticleslgStudy

biology

Paul M. Bingham

Paul M. Bingham is a biology topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Paul M. Bingham rather than just read about it. In short: Paul Montgomery Bingham (born February 25, 1951) is an American molecular biologist and evolutionary biologist, Associate Professor in the Department of Biochemistry and Cell Biology at Stony Brook University and Vice President for Research at Rafael Pharmaceuticals. He is known for his work in molecular biology, and has also published recent articles and a book on human evolution.

Key takeaways

  • Paul M. Bingham belongs to biology; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Paul M. Bingham to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Paul M. Bingham from memory before moving on to harder problems.

Reference excerpt

Paul Montgomery Bingham (born February 25, 1951) is an American molecular biologist and evolutionary biologist, Associate Professor in the Department of Biochemistry and Cell Biology at Stony Brook University and Vice President for Research at Rafael Pharmaceuticals. He is known for his work in molecular biology, and has also published recent articles and a book on human evolution.

Biography Bingham received his undergraduate degree at Blackburn College in Carlinville, Illinois, and then completed his PhD in Biochemistry and Molecular Biology at Harvard University in 1980 (thesis advisor, Matthew Meselson) after completing an MS in Microbiology at the University of Illinois (with John W. Drake). He spent two years at the National Institute of Environmental Health Sciences (NIEHS) before joining the faculty of the Department of Biochemistry and Cell Biology and the School of Medicine at Stony Brook University in 1982.

Molecular biology He was part of a collaborative team that discovered the parasitic DNA sequence element, the P element transposon. This enabled a widely used strategy still used today for retrieving genes from animals. It also shed fundamental new light on how evolution shapes the (self-interested) individual genes that collaborate to build organisms. With his wife (Zuzana Zachar), he demonstrated that transposon insertion mutations were responsible for most of the alleles used in the development of classical genetics. He also collaborated with Carl Wu and Sarah Elgin (then at Harvard) on fundamental properties of metazoan chromatin structure. In collaboration with Margaret Kidwell, then at Brown University, and Gerry Rubin, then at the Carnegie Institution, he carried out the molecular cloning of the P element transposon in Drosophila. This work revolutionized the retrieval of genes in Drosophila and subsequently contributed to progress in metazoan molecular and developmental genetics. He and his collaborators were the first to propose the use of P element transposon tagging to clone the first metazoan RNA polymerase subunit. This work demonstrated that the P element is a recently invading parasite of the Drosophila genome and gene pool. Thus, P became the first clearly defined metazoan example of this long-suspected phenomenon. His research group also worked on the nature of metazoan gene regulation and the elucidation of the first case of autoregulation of gene expression at the level of pre-mRNA splicing and of critical features of the nuclear organization of pre-mRNA processing and transport This latter work first clearly established the now-widely accepted model of channeled diffusion for the movement of most pre-mRNAs through the nuclear compartment. Bingham and Zachar discovered the first-in-class anti-cancer mitochondrial metabolism drug (CPI-613; devimistat), currently in Phase III registrational clinical trials in pancreatic ductal adenocarcinoma and acute myeloid leukemia. This work is now being done in collaboration with Rafael Pharmaceuticals.

Human evolutionary biology In the mid-1990s, he developed a theory of human uniqueness that proposes a novel explanation of why humans have evolved to be ecologically dominant. The theory has been published in three peer-reviewed journals: The Quarterly Review of Biology, Evolutionary Anthropology and the Journal of Theoretical Biology. He and co-author Joanne Souza have developed the theory further in a self-published book, Death from a Distance and the Birth of a Humane Universe. This work builds on W.D. Hamilton's theory of kin selection (Benefit x Relatedness > Cost) and posits that the genus Homo evolved when an ancestral organism developed the ability to effectively manage non-kin conflicts of interests by lowering the cost of coercion between non-kin individuals (Benefit > Cost of Coercion + Cost of Cooperation). The theory, using precedents established in biological theory, proposes to explain many aspects of human social and sexual behavior. It proposed to account for the evolution of the human species from the advent of its phylogenetic branching from other hominins through physiological and behavioral adaptations until our current civilization. This theory of human uniqueness claims to answer the fundamental scientific challenge posed by Charles Darwin, to explain the descent of man: how did the 'incremental' process of evolution by natural selection suddenly produce an utterly unprecedented kind of animal, humans? It suggests an explanation of human origins, and also of human properties (from speech to political/economic/religious behavior). According to his theory, the cost to an enforcer of coercing a cheating individual into a cooperative effort, known as the free-rider problem, was lowered when a precursor species to humans developed a way to threaten adult conspecifics from a distance by evolving the ability to throw projectiles with sufficient skill to reliably injure the cheater, especially conjointly with others. This reduced the personal risk to multiple enforcers as formulated by Lanchester's Square Law, when they gang up on a cheater.

The theory proposes that this elite throwing ability initially allowed bands of proto-humans improved capacity to repel predators and scavenge their kills in the African savanna. It was later adapted as threat projection towards free-riding conspecifics (cheaters) in non-kin cooperative groups that made the cooperation evolutionarily stable against cheaters who, without coercion by this threat, would otherwise flourish and displace co-operators. The theory further generalizes to a theory of history, claiming to account for many salient events of the two-million-year course of the human lineage—from the evolution of the genus Homo to the inception of behavioral modernity to the Neolithic Revolution to the rise of the nation-state.

Academic work In collaboration with Joanne Souza, he has developed a course [1] on the logic and implications of this new theory [2]. Bingham has served as the Faculty Director of the Freshmen College of Human Development at Stony Brook [3]. Bingham also serves on the management team of Rafael Pharmaceuticals, a firm developing cancer therapies, as Vice President of Research. He and his collaborator, Prof. Zuzana Zachar, recently received the Maffetone Research Prize from the Carol M. Baldwin Breast Cancer Research Fund for their cancer work.

Publications

Social coercion theory

Cancer research

References

… excerpt ends here. Continue reading the full article.

Worked examples

Example 1 — a first encounter with Paul M. Bingham

Start with the simplest possible case. Write down what Paul M. Bingham claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In biology, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Paul M. Bingham before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Paul M. Bingham ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Paul M. Bingham

In research
Paul M. Bingham appears in biology research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Paul M. Bingham in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Paul M. Bingham is common in secondary-school and first-year university syllabi. It links to neighbouring topics 1951 births, 21st-century American biologists, American evolutionary biologists, so understanding it makes those chapters shorter.
In everyday life
Look for Paul M. Bingham outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
Ask Teacher Smith questions about this articleOpens your AI tutor with a question about “Paul M. Bingham” →

Affiliate

Preply — study more efficiently by working with a personal tutor. 50% off.

How to study Paul M. Bingham in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Paul M. Bingham means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Paul M. Bingham out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Paul M. Bingham in simple terms?

Paul Montgomery Bingham (born February 25, 1951) is an American molecular biologist and evolutionary biologist, Associate Professor in the Department of Biochemistry and Cell Biology at Stony Brook University and Vice President for Research at Rafael Pharmaceuticals. He is known for his work in mol…

Why does Paul M. Bingham matter?

Because it connects several biology ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Paul M. Bingham?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Paul M. Bingham.

Tags

  • 1951 births
  • 21st-century American biologists
  • American evolutionary biologists
  • American molecular biologists
  • Blackburn College (Illinois) alumni
  • Harvard Medical School alumni
  • Human evolution theorists
  • Living people
  • Stony Brook University faculty
  • University of Illinois System alumni

Keep exploring