Fig 1.
Classical view of genotype–phenotype.
In this view, a protein or the gene product is considered to have one shape with a single function. Monogenic traits are expressed by single genes, whereas polygenic traits are affected by multiple genes. Seemingly unrelated phenotypic traits are pleiotropy that can be expressed by a single gene.
Fig 2.
Network perturbations of genotype–phenotype.
Mutations can shift phenotype traits generated from wild-type trait (upper panel), affecting solely the protein (a “node”) or protein–protein interaction (an “edge”). The former and latter are node and edge mutations, respectively. The node mutation (middle panel) generates a monogenetic trait, whereas the edge mutation (bottom panel) creates or breaks the protein–protein interactions yielding monogenetic or polygenetic traits. An example shown for edge trait is polygenetic.
Fig 3.
New paradigm of genotype–phenotype.
In this view, genotype encodes a distinct conformational ensemble in all states. Populations determine the specific phenotype traits that link to genotype. Mutations shift the equilibrium of preexisting conformational ensembles altering phenotypes.
Fig 4.
The network controls the transcriptional regulation for gene. Edge mutations can alter the cellular network, expressing the end-product phenotype.
Fig 5.
Phenotype switch of HIV-1 entry.
Schematic diagram representing the initial process of the HIV-1 entry that led to fusion between the viral and the host cell membranes. The gp120 trimer undergoes a conformational change upon binding to cellular receptor CD4, exposing the variable loop V3. The V3 loop binds to the coreceptor (CCR5 and CXCR4), triggering the entry process. The wild-type V3 loop with positively and negatively charged residues at positions 304 and 322, respectively, recognizes CCR5. A phonotype switch by a mutation from a negatively to a positively charged residue at position 322 in the V3 loop alters coreceptor recognition to CXCR4. Modeled structures are the crystal structures of gp120 (PDB code: 24BC), CCR5 (PDB code: 4MBS), and CXCR4 (PDB code: 3ODU) and the NMR structure of V3 loop (PDB code: 2ESX). CCR5, C-C chemokine receptor type 5; CXCR4, C-X-C chemokine receptor type 4; PDB, Protein Data Bank.