Gene-centrism (defined as genes create and control the organism) is
bad biology, not because it is an ideology or a philosophy, but because it
is an incorrect description of what happens in a cell. Gene-centrism is
embedded in the language in which biologists usually write and think about
DNA. In order to eliminate gene-centrism, we need to take a fresh look
at the role of DNA in cells and organisms. Criticisms such as "DNA is not the book of life" and "DNA is not a
blueprint" are too vague and ineffective.
Here is an example of DNA centrism:
"Central to this are enhancers and promoters, DNA sequences that
dictate the location, timing, and intensity of gene expression."
from: A tighter grip on gene expression, Science 3 Jul 2025.
Please note: "dictate"! and "timing"! Especially, 'timing' is
mysterious. How do DNA sequences dictate timing? I asked the author. No
reply. I think this is a sloppy language caused by a mindless DNA-centric
view. In general, the question is not asked: Does the genome control the
cell? Or does the cell control the genome? Since 'the genome controls the
cell' seems to be the default position, it is not a well-argued position.
Therefore, it is better to refer to 'causes' than 'reasons' for
gene-centrism. [4]
The many 'causes' of gene-centrism:
-
Gene-centrism became the de facto paradigm in biology because of the successes of
Mendelian genetics, population genetics and the theory of
evolution.
-
The discovery of the structure of DNA by Watson and Crick and the
subsequent unravelling of the genetic code transformed gene-centrism in DNA-centrism.
-
Crick's Central Dogma of molecular biology established that DNA is
the source of information.
-
Mutations in DNA were found to be the main source of hereditary
variation
-
Natural selection acts upon heritable variations. Without
hereditary variation evolution comes to a standstill.
-
Adaptation. Every phenotypic change that is not
inherited, is lost.
-
The success of Dawkins' The Selfish Gene entrenched
gene-centrism in evolutionary thinking.
-
DNA sequencing became the most important method in evolutionary
research (evolutionary relationships, phylogenetic trees, ancient
DNA)
-
Evolutionary Developmental biology (evo-devo): homeobox (hox)
genes explain how genes build the organism (the body plan)
[5].
-
Clinical genetics showed again and again that hereditary diseases were
caused by mutations in DNA and that DNA-therapy is the cure for genetic
diseases
-
SARS-CoV-2 has shown dramatically that viruses, which only
contain DNA or RNA, have control over our bodies. mRNA COVID-19 vaccines
have shown that mRNA is the active ingredient.
-
Identical twins: Why do identical twins look more alike than
non-identical twins? Is there a better proof of the power of DNA than
this?
-
Synthetic genomes control the host cell [3]
-
Genetic engineered bacteria, plants and animals produce new
drugs and other chemicals, demonstrating the creative power of
DNA again. (Recombinant DNA).
In 1859 there was a big hole in Darwin's theory of evolution. He lacked a
theory of heredity. In 1900 Mendelian genetics, and in 1953 the double-helix
filled in the hole and transformed biology. Now, biology has a solid theory
of heredity. DNA transformed the theory of evolution, too. The opposite of Darwin's theory has become true: DNA quickly became the
centerpiece of the theory of evolution. Yet, this centerpiece obstructed a
clear view of the actual role of DNA in organisms.
Objections to gene- and DNA-centrism:
-
Power. Genes have no catalytic capacity, only enzymes have the power to
catalyse biochemical reactions. From a biochemical point of view, genes do not have the power to do
anything. Why? To perform its function, DNA must be stable. DNA
must reliably store sequences. DNA is a repository safely housed in the
cell nucleus. DNA is passive in the sense that it doesn't initiate
biochemical reactions. DNA is acted upon by other molecules: proteins and
enzymes. The only 'active' thing DNA does is Watson-Crick base
pairing.
-
Crick's Central Dogma of molecular biology established that
DNA is the source of information, but not the cause of building and maintaining the organism
[5].
-
Replication: "Replication is the goal of selfish genes. Selfishness is a metaphor for
the relentless drive of a gene to be copied and passed on to the
next generation". Wrong! Genes cannot copy themselves, because that requires enzymes (polymerases). The famous Watson-Crick base pairing is by far
insufficient for DNA copying fidelity [1]. Furthermore, DNA replication
is a replication of whole chromosomes and whole genomes (never
individual genes and chromosomes) and is intrinsically linked to
cell-division [7].
-
DNA-repair is performed by repair-enzymes [1].
-
Natural selection does not act directly on genes. There are no
free floating genes in nature upon which natural selection could act. We
do not see naked DNA in nature. Genes are always part of genomes, and
genomes are always part of individual organisms. Natural selection can
only act on phenotypes. Genes can only have effects through the
proteins they encode.
-
Evolution. Evolution is usually defined as a change
in gene frequency in populations of organisms over generations. The
language of population genetics is just a kind of
bookkeeping. It suggests that genes are all that matter. However, population genetics does not reflect reality. It is an abstract mathematical language. If
that implies that genes construct and control our bodies
and therefore explain evolution, then it is a misleading
language.
- Multi-cellularity: The transition from single cell to multi-cellular organisms was a major step in evolution. All plants and animals are multi-cellular organisms. [8].
-
Reproduction. Genes and genomes can be copied, but only
individual organisms reproduce. Reproduction is at the organism level.
Survival of the fittest individual. Fitness is reproductive
success of individuals. Furthermore, what is transmitted to the next
generation is never a naked genome, but a genome is always embedded in a sperm and egg cell. Egg cells
contain more information and resources than the information present in
DNA.
-
Splicing. Genes of eukaryotes contain introns and exons.
Most eukaryotes use protein-assisted splicing of genes. The
selection of splice sites is done by splicing activator and splicing
repressor proteins.
-
Evolutionary Developmental biology (evo-devo): genes do not
build the body. Hox genes produce proteins, but there is still a gap in
understanding how those proteins build a three-dimensional body. A genetic explanation is not sufficient
[5].
-
Clinical genetics: DNA and chromosomal mutations are indirect
causes of disease. The ultimate effects are on the level of
proteins, cells, tissues, organs and the organism level. The ultimate
causes of mutations are cellular processes. [6]
-
Gene-therapy, DNA- and RNA-vaccines: although DNA or RNA are the
so-called 'active' substances, in the end, the real active component is
always a protein. The proteins do the work.
Summary
It would be foolish to deny that DNA is an indispensable component of
life on earth. But that does not mean that DNA has the power to
create and control the development and maintenance of
organisms. DNA is not the Uncaused First Cause!
DNA is the source, but not the cause! Writing and thinking about DNA should be free of this kind of
bias. The supposed arguments for DNA-centrism are not arguments at all, but just sloppy language. Others
[2] have criticized DNA-centrism inadequately. In a follow-up post, I will
deal with 'the selfish gene'.
8 Mar 2026 minor text edit.
Notes
-
Kondrashov: "Despite its beauty, Watson-Crick complementarity is absolutely
insufficient to ensure an acceptable fidelity of replication, even with
perfect raw materials. ... Fortunately, fidelity of nucleotide
attachment depends not on complementarity, but on active involvement of
DNA polymerases." see my blogs: Famous Watson-Crick base pairing is by far insufficient for DNA
copying fidelity, 20 Jan 2023 and
Two Nobel Prizes contradicting each other: Watson and Crick versus
Tomas Lindahl 5 Jan 2023.
-
For recent criticism, see for example: Philip Ball (How Life Works. A User's Guide to the New Biology) and Denis Noble (The Music of Life. Biology beyond the Genome). Both authors tend to go too far in their criticism. Noble is a
biologist, and Ball holds a degree in chemistry and a PhD in physics. In
2024, I posted 3 blogs about Ball's book, see
overview page of all DNA blog posts.
-
Daniel Gibson (2010)
Creation of a Bacterial Cell Controlled by a Chemically
Synthesized Genome, Science, 20 May 2010: "...its transplantation into a
M. capricolum recipient cell to create new
M. mycoides cells that are controlled only by the
synthetic chromosome." My emphasis. Please note: "controlled"!
The genome controls the cell ! And not: the host cell is
able to control the synthetic genome! This heading is a beauty:
Let There Be Life ! As if a genome creates life! added 18 Dec 2025
-
Thanks to an email from Rolie Barth, I added the last few
sentences for clarification 18 Dec 2025
-
added 21 Dec 2025
-
For example,
Cystic fibrosis
(CF) is a hereditary disease (a deletion of 3 bases) which results in a
faulty membrane protein.
Even chromosomal disorders such as
trisomy-21
or
fragile-X syndrome
are not the direct cause of a disease; the effects are on cell,
tissue, organ and organism level. The symptoms are difficult or
impossible to predict on the basis of DNA alone. Importantly,
mutations in DNA are not the 'uncaused first cause':
mutations are caused by error-prone replication (enzymes),
faulty DNA-repair (enzymes) or genetic recombination
(enzymes). In humans, there are 9 major proteins involved in UV induced
DNA damage. These are cellular processes. [Added 31 Dec 2025]
- Mitosis and meiosis are complicated cellular processes regulated at the cellular level. [Added 6 March 2026]
- The emergence of multicellularity mounts a challenge not only to the gene-centric view of biology but, significanlty, against the gene's-eye view of evoloution (Alfonso Martinez Arias (2023) 'The Master Builder. How the New Science of the Cell is Rewriting the Story of Life). [Added 6 March 2026]
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