Wild fish thrive despite 'hopeless monster' mutations, according to study

Wild fish thrive despite ‘hopeless monster’ mutations, according to study
Genetic mapping, expression and role of HOXD11B in stickleback dorsal spine development. a, Gasterosteus mapping cross. b, QTL scan results for spine number and spine length. x axis: Gasterosteus chromosomes; y axis: LOD score for three- versus four-spine trait (top), length of DS2 (bottom). The QTL peak on chromosome 6 includes the HOXDB cluster (gene diagram at the bottom, scale bar, 1 kb). The peak on chromosome 4 includes the EDA-MSX2A-STC2A cluster described elsewhere . Dashed lines: genome-wide significance thresholds from permutation testing. c, Integration of GFP reporter using CRISPR–Cas9 upstream of the endogenous HOXD11B locus of low-spine Gasterosteus. Plasmid: gray; eGFP: green; basal hsp70 promoter: blue; chromosomal locus: black. Scale bar, 100 bp. TSS, transcription start site. d, eGFP expression in posterior half of fish at the stage when the dorsal spines are forming (Swarup stage 31). Scale bar, 1 mm. e, Note expression in fin fold between DS2 and DSL, DSL and dorsal fin (DF). Scale bar, 1 mm. f, X-ray of uninjected Gasterosteus (top) and Gasterosteus injected at the single-cell stage with Cas9 and sgRNA targeting the coding region of HOXD11B (bottom). Arrows: two blank pterygiophores are often located between DS2 and DSL but only in uninjected fish (insets: two blank pterygiophores in n = 5 out of 18 control and n = 0 out of 23 injected F0 mutants, two-tailed Fisher's exact test P = 0.01). Scale bar, 5 mm. g, Length comparisons of dorsal and anal spines. Box and whisker plot: center line, median; box limits, interquartile range (IQR); whiskers, 1.5× IQR; individual measurements shown as single points (circles: WT; triangles: mutant). y axis: residuals after accounting for standard length of fish . DSL and AS were significantly longer in injected than uninjected fish (two-tailed t-test Bonferroni-corrected at α = 0.05, n = 18 control and n = 23 injected, DSL Padj  = 3 × 10−5, AS Padj = 0.02). DS1 and DS2 lengths were not significantly different. Credit: Nature Ecology & Evolution (2022). DOI: 10.1038/s41559-022-01855-3

A series of experiments led by researchers at Stanford Medicine that included fish hookups, CRISPR and lake hopping has confirmed a long-standing, yet unproven, assumption about natural evolution. It also debunks a talking point favored by proponents of intelligent design, who have argued that naturally occurring mutations will only damage or destroy an animal and can't lead to useful new traits and body structures.

The researchers identified repeated changes in the regulation of a key developmental gene that increase the number and govern the length of the major defensive spines of a called the stickleback. New spine traits improve the fish's survival in the face of varying predators—flying in the face of a key assertion by anti-evolutionists that major changes will always leave animals unfit to survive in the wild.

"Scientists already know that changes in the regulation of this gene, called HOX, control the development of major body structures during development," said David Kingsley, Ph.D., professor of developmental biology. "What's new is that we conclusively show that mutations in this gene produce major changes in —new features that help fish thrive in natural environments. Our findings refute the common argument that these types of genes are so important, so fundamental, that animals with mutations in these regions wouldn't survive in nature—that if you play with master regulators, you're only going to make a hopeless monster."

Kingsley, an HHMI investigator and the Rudy J. and Daphne Donohue Munzer Professor, is the senior author of the research, which was published online Sept. 1 in Nature Ecology and Evolution. Graduate student Julia Wucherpfennig is the lead author of the study.

Although the concept of evolution is widely accepted, it can happen in different ways. Regressive evolution is the loss of existing, previously useful but now disadvantageous or useless traits, resulting in an animal that is more suited to its natural environment. These changes are almost always either neutral—think about cave fish that have lost their eyes after generations in darkness—or helpful, as in ' shedding the hairy suit of our ape relatives, enabling us to chase prey for long distances without becoming overheated.

A game of chance

In contrast, progressive evolution occurs when organisms acquire new traits that allow them to outcompete their peers. But such changes are essentially a leap of faith equivalent to rolling the genetic dice and hoping they all come up sixes. Smaller, more gradual changes are less risky. Big structural changes, sometimes called large-effect mutations, can be particularly dicey: Imagine one day you strut out of your apartment sporting a third leg, or two heads. Would you have an advantage over your neighbors when you run for the bus, or are you more likely to trip and fall head(s)-first into traffic?

Although there have been some instances in which animals have gained beneficial traits in nature from changes in HOX genes—fruit flies evolved specific patterns of sensory bristles on their legs and some honeybees gained distinctive coloring on their abdomens—most major structural gains caused by mutations in these regions have been detrimental.

Wild fish thrive despite ‘hopeless monster’ mutations, according to Stanford-led study
Julia Wucherpfennig found that genetic variations in stickleback fish were associated with major anatomical changes, notably in the number of spines. Credit: David Kingsley

"Laboratory-bred four-winged are a famous example of how relatively simple genetic alterations in regulatory regions of the HOX genes can dramatically change the body shape of an animal," Kingsley said. "But because these flies can't survive in the wild, anti-evolution proponents have seized on them—not as good examples of how genes drive evolution, but as proof that gene changes can only make animals less functional."

Two- to four-inch-long stickleback fish, which sport varying numbers of pointy spines along their backs, are great research subjects because they evolve rapidly and dramatically in response to changing environmental conditions. A lake rife with fish-eating insects often houses sticklebacks with fewer and shorter spines to grab. But a pond with larger fish or birds that swallow their fish sticks whole is likely to boast a population of sticklebacks with longer, more numerous, throat-scratching spines. Forests of watery weeds are great for flexible, slippery fish who can hide in the vegetation, while in the open ocean, armored plates and formidable spines are the way to go.

The Kingsley lab started the study with a spot of watery matchmaking. Previous graduate students crossed a two-spined female stickleback from a in British Columbia with a three-spined male stickleback from the salty waters of Bodega Bay, California. They then crossed the progeny from that match with one another and analyzed the number and shape of their spines. Most of the 590 grand-fish had three spines, but six had two spines and 21 had four spines—more than any of their ancestors. Extensive genetic studies of the variably spined fish pinpointed differences in the region around a gene called HOXDB, which is a member of the HOX family of .

A link between genes and anatomy

Wucherpfennig continued collecting and crossing sticklebacks from myriad North American lakes and streams, studying their genetic makeup and using CRISPR methods to confirm the effects of the HOXDB gene on dorsal spines. She found a panel of changes in regions near the HOXDB gene and showed they were associated with major anatomical changes that are evolving in the defensive armor of wild fish.

"In Nova Scotia, some of the stickleback populations have evolved to have five or even six spines," Kingsley said. "Nature left the coding region of this gene intact but altered how and when it is expressed during normal development to add structures rather than stripping them away. And fish with these new structures are thriving in a completely wild environment subjected to a whole range of environmental pressures."

Wucherpfennig and her colleagues showed that repeated changes in the regulatory regions of the HOXDB gene are responsible for the recent evolution of new spine patterns in two different stickleback species she studied from across North America. They are now interested in learning whether similar changes are responsible for differences in fish that are even more distantly related.

"Are there predictable rules that govern evolutionary change?" Kingsley said. "Are natural species using the same trick over and over, or do they have to invent a new trick each time? So far, it's been the same gene even in these very divergent sticklebacks from different environments. Here we show that nature routinely adds major structures to generate animals that are more suited to the environment, and that it does so repeatedly using the same master regulatory gene. It's a decisive argument for progressive evolution, which has been debated in academic and non-academic circles for decades."

More information: Julia I. Wucherpfennig et al, Evolution of stickleback spines through independent cis-regulatory changes at HOXDB, Nature Ecology & Evolution (2022). DOI: 10.1038/s41559-022-01855-3

Journal information: Nature Ecology & Evolution

Citation: Wild fish thrive despite 'hopeless monster' mutations, according to study (2022, September 8) retrieved 25 June 2024 from https://phys.org/news/2022-09-wild-fish-hopeless-monster-mutations.html
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