Scientists have created "daddy shortlegs," a stunted version of the common household pest daddy longlegs, by suppressing the genes behind the arachnid's famously elongated limbs.
Daddy longlegs, also known as harvestmen, belong to the class Arachnids — a group of eight-legged invertebrates that includes spiders, scorpions, ticks, mites and horseshoe crabs. There are more than 6,500 species of daddy longlegs in the order Opiliones, each of which is characterized by flexible legs that are several times longer than the individual's body.
In a series of new experiments, a team of researchers mapped the entire genome of Phalangium opilio, the most common species of daddy longlegs, and isolated the genes responsible for their famous long legs. The researchers then turned off the long leg genes in developing embryos, creating individual arachnids with shorter, deformed legs.
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"Our purpose was not just to shorten their legs just for the sake of it," lead author Guilherme Gainett, a graduate student at the University of Wisconsin-Madison, told Live Science. "We wanted to understand more about how these fascinating creatures evolved their alien way of locomotion and body plan."
Unlike true spiders, daddy longlegs don't use all eight of their legs for walking; instead, they use three pairs for locomotion and the remaining, and longest, pair, they wave around to feel their way around, Gainett added.
Once that was done, researchers searched the DNA map for genes likely to cause long legs, by comparing the P. opilio genome with the genomes of other insects, such as the fruit fly (Drosophila melanogaster), in which scientists had already figured out which genes code for legs, Gainett said.
The comparison revealed two Hox genes — a group of related genes that code for specific body parts during embryonic development — known as Deformed (Dfd) and Sex combs reduced (Scr), that were tied to leg development in other species.
Therefore, the researchers down-regulated these genes in developing embryos to see if the change would interfere with the development of their long legs.
To do this they used a process known as RNA interference, which is inspired by a process living cells use to ward off viruses. When viruses invade cells, a protein structure known as the RISC complex identifies the invaders' double-stranded RNA. The cell can then target and turn off the corresponding messenger RNA (mRNA), single-stranded RNA used to help transcribe or read genes, which viruses use to reproduce within the cell, Gainett said.
However, organisms also produce mRNA to create new proteins. So the scientists repurposed the RISC complex to silence the mRNA of the Dfd and Scr by disguising those genes as viruses.
"By synthesizing artificial double-stranded RNA matching your gene of interest and injecting it into the embryo, it is possible to interfere with the expression of that gene," Gainett said.
"When the Hox genes are down-regulated these leg appendages transform into short food-manipulating appendages called pedipalps," Gainett said.
In addition to being much shorter than their normal legs, pedipalps have six segments, instead of the usual seven in regular legs; pedipalps also lack special joints known as tarsomeres, which give their legs the flexibility needed to properly move around and help sense the world around them, Gainett said.
However, not all the embryos' legs became shorter. The fourth pair of legs still grew to their usual length. "This is because the fourth pair of legs likely requires the input of a third Hox gene to set up their fate," Gainett said. "This is something that we are currently investigating," he added.
Some of the deformed embryos hatched with their shortened legs, but they all died before reaching adulthood, Gainett said.
Gainett hopes that the findings could also lead to breakthroughs in understanding other arachnid body parts.
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"I think future studies have the potential to clarify how other unique structures of arachnids are formed, such as the chelicera [fangs in spiders]," Gainett said.
The study was published online Aug. 4 in the journal Proceedings of the Royal Society B.
Originally published on Live Science.