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新しい研究では、染色体構造に基づく独自のアプローチを使用して、有櫛動物としても知られるクシクラゲが動物の生命の樹から分岐した最初の系統であり、カイメンが次の枝として続くことを明らかにした。 これまでは、遺伝子配列の研究が決定的ではなかったため、カイメンが最初の分岐なのか、それともクシクラゲが最初の分岐なのかは不明であった。 この研究は、動物の初期進化の理解に貢献し、神経系、筋肉、消化管などの動物生物学の主要な特徴の起源についての洞察を提供します。
染色体分析により、すべての動物の姉妹グループに関する議論が解決されます。 スポンジではなくクシゼリーです。
研究者らは、染色体に基づく新しいアプローチを用いて、クシクラゲが海綿動物に先立って動物の生命の樹から分岐した最初の系統であることを明らかにした。 この研究は、動物の初期進化に関する新たな洞察を提供し、重要な生物学的特徴がどのように進化したかについての理解を深めます。
生物学者たちは1世紀以上にわたり、5億年以上前に古代の海に最初に誕生した最初期の動物はどのようなものだったのか疑問に思ってきた。
科学者たちは、今日最も原始的に見える動物の中から動物の生命の樹の最も初期の枝を探し、その可能性を徐々に 2 つのグループに絞り込みました。1 つは成体になってから一生を 1 か所で過ごし、海水から食物をろ過する海綿動物です。 そして、クシクラゲは、食物を求めて世界中の海を漕いで進む貪欲な捕食者です。
今週ジャーナルに発表された新しい研究では 自然研究者らは、染色体構造に基づいた新しいアプローチを使って決定的な答えを導き出した。クシクラゲ、または有櫛動物(ティーン・ア・フォア)は、動物の系統から分岐した最初の系統だった。 次に海綿動物が続き、人類につながる系統を含む他のすべての動物が多様化しました。
研究者らは有櫛動物の系統が海綿動物より前に分岐したと判断したが、両グループの動物は共通の祖先から進化し続けてきた。 それにもかかわらず、進化生物学者は、これらのグループは依然として初期の動物と特徴を共有しており、動物の生命の樹のこれらの初期の枝を研究することで、動物がどのように発生し、多様性に進化したのかを解明できると信じています。[{” attribute=””>species we see around us today.

Hormiphora californensis, called the California sea gooseberry, is a comb jelly, or ctenophore, common in California coastal waters. Ctenophores have eight sets of cilia running down their side, which they use to propel themselves through the oceans in search of food. This specimen was observed on 2016 by MBARI’s remotely operated vehicle (ROV) Doc Ricketts in the Monterey Canyon at a depth of approximately 280 meters. Credit: Monterey Bay Aquarium Research Institute
“The most recent common ancestor of all animals probably lived 600 or 700 million years ago. It’s hard to know what they were like because they were soft-bodied animals and didn’t leave a direct fossil record. But we can use comparisons across living animals to learn about our common ancestors,” said Daniel Rokhsar, University of California, Berkeley professor of molecular and cell biology and co-corresponding author of the paper along with Darrin Schultz and Oleg Simakov of the University of Vienna. “It’s exciting — we’re looking back deep in time where we have no hope of getting fossils, but by comparing genomes, we’re learning things about these very early ancestors.”
Understanding the relationships among animal lineages will help scientists understand how key features of animal biology, such as the nervous system, muscles and digestive tract, evolved over time, the researchers say.
“We developed a new way to take one of the deepest glimpses possible into the origins of animal life,” said Schultz, the lead author and a former UC Santa Cruz graduate student and researcher at the Monterey Bay Aquarium Research Institute (MBARI) who is now a postdoctoral researcher at the University of Vienna. “This finding will lay the foundation for the scientific community to begin to develop a better understanding of how animals have evolved.”

A newly discovered and still undescribed bioluminescent deep-sea sponge observed in 2019 by MBARI’s ROV Doc Ricketts offshore of Central California at a depth of approximately 3,970 meters. Credit: Monterey Bay Aquarium Research Institute
What’s an animal?
Most familiar animals, including worms, flies, mollusks, sea stars, and vertebrates — and including humans — have a head with a centralized brain, a gut running from mouth to anus, muscles and other shared features that had already evolved by the time of the famed “Cambrian Explosion” around 500 million years ago. Together, these animals are called bilaterians.
Other bona fide animals, however, such as jellyfish, sea anemones, sponges, and ctenophores, have simpler body plans. These creatures lack many bilaterian features — for example, they lack a defined brain and may not even have a nervous system or muscles — but still share the hallmarks of animal life, notably the development of multicellular bodies from a fertilized egg.
The evolutionary relationships among these diverse creatures — specifically, the order in which each of the lineages branched off from the main trunk of the animal tree of life — has been controversial.
With the rise of DNA sequencing, biologists were able to compare the sequences of genes shared by animals to construct a family tree that illustrates how animals and their genes evolved over time since the earliest animals arose in the Precambrian Period.
But these phylogenetic methods based on gene sequences failed to resolve the controversy over whether sponges or comb jellies were the earliest branch of the animal tree, in part because of the deep antiquity of their divergence, Rokhsar said.
“The results of sophisticated sequence-based studies were basically split,” he said. “Some researchers did well-designed analyses and found that sponges branched first. Others did equally complex and justifiable studies and got ctenophores. There hasn’t really been any convergence to a definitive answer.”
Just looking at them, sponges seem quite primitive. After their free-swimming larval stage, they settle down and generally remain in one place, gently sweeping water through their pores to capture small food particles dissolved in sea water. They have no nerves or muscles, though their hard parts make nice scrubbers in the bath.
“Traditionally, sponges have been widely considered to be the earliest surviving branch of the animal tree, because sponges don’t have a nervous system, they don’t have muscles, and they look a little bit like colonial versions of some unicellular protozoans,” Rokhsar said. “And so, it was a nice story: First came the unicellular protozoans, and then sponge-like multicellular consortia of such cells evolved and became the ancestor of all of today’s animal diversity. In this scenario, the sponge lineage preserves many features of the animal ancestor on the branch leading to all other animals, including us. Specializations evolved that led to neurons, nerves and muscles and guts and all those things that we know and love as the defining features of the rest of animal life. Sponges appear to be primitive, since they lack those features.”
The other candidate for earliest animal lineage is the group of comb jellies, popular animals in many aquariums. While they look superficially like jellyfish — they often have a bell-like shape, although with two lobes, unlike jellyfish, and usually tentacles — they are only distantly related. And while jellyfish squirt their way through the water, ctenophores propel themselves with eight rows of beating cilia arranged down their sides like combs. Along the California coast, a common ctenophore is the 1-inch-diameter sea gooseberry.
Chromosomes to the rescue
To learn whether sponges or ctenophores were the earliest branch of animals, the new study relied on an unlikely feature: the organization of genes into chromosomes. Each species has a characteristic chromosome number — humans have 23 pairs — and a characteristic distribution of genes along chromosomes.
Rokhsar, Simakov, and collaborators had previously shown that the chromosomes of sponges, jellyfish and many other invertebrates carry similar sets of genes, despite more than half a billion years of independent evolution. This discovery suggested that chromosomes of many animals evolve slowly, and allowed the team to computationally reconstruct the chromosomes of the common ancestor of these diverse animals.
But the chromosome structure of ctenophores was unknown until 2021, when Schultz — then a graduate student at UC Santa Cruz — and his co-advisers, Richard Green of UCSC and Steven Haddock of MBARI and UCSC, determined the chromosome structure of the ctenophore Hormiphora californiensis. It looked very different from those of other animals, which posed a puzzle, Rokhsar said.
“At first, we couldn’t tell if ctenophore chromosomes were different from those of other animals simply because they’d just changed a lot over hundreds of millions of years,” Rokhsar explained. “Alternatively, they could be different because they branched off first, before all other animal lineages appeared. We needed to figure it out.”
The researchers joined forces to sequence the genomes of another comb jelly and sponge, as well as three single-celled creatures that are outside the animal lineage: a choanoflagellate, a filasterean amoeba and a fish parasite called an ichthyosporean. Rough genome sequences of these non-animals already existed, but they did not contain the critical information needed for chromosome-scale gene linkage: where they sit on the chromosome.
A smoking gun
Remarkably, when the team compared the chromosomes of these diverse animals and non-animals, they found that ctenophores and non-animals shared particular gene-chromosome combinations, while the chromosomes of sponges and other animals were rearranged in a distinctly different manner.
“That was the smoking gun — we found a handful of rearrangements shared by sponges and non-ctenophore animals. In contrast, ctenophores resembled the non-animals. The simplest explanation is that ctenophores branched off before the rearrangements occurred,” he said.
“The fingerprints of this ancient evolutionary event are still present in the genomes of animals hundreds of millions of years later,” Schultz said. “This research … gives us context for understanding what makes animals animals. This work will help us understand the basic functions we all share, like how they sense their surroundings, how they eat and how they move.”
Rokhsar emphasized that the team’s conclusions are robustly based on five sets of gene-chromosome combinations.
“We found a relic of a very ancient chromosomal signal,” he said. “It took some statistical detective work to convince ourselves that this really is a clear signal and not just random noise, because we’re dealing with relatively small groups of genes and perhaps a billion years of divergence between the animals and non-animals. But the signal is there and strongly supports the ‘ctenophore-branched-first’ scenario. The only way the alternative sponge-first hypothesis could be true would be if multiple convergent rearrangements happened in both sponges and non-ctenophore animals, which is very unlikely.”
For more on this research, see Genetic Linkages Illuminate Earliest Animal Evolution.
Reference: “Ancient gene linkages support ctenophores as sister to other animals” by Darrin T. Schultz, Steven H. D. Haddock, Jessen V. Bredeson, Richard E. Green, Oleg Simakov and Daniel S. Rokhsar, 17 May 2023, Nature.
DOI: 10.1038/s41586-023-05936-6
Jessen Bredeson of UC Berkeley also contributed to this work.
Funding for this research was provided by the David and Lucile Packard Foundation, MBARI, the National Science Foundation (GRFP DGE 1339067 and DEB-1542679), the European Research Council’s Horizon 2020: European Union Research and Innovation Programme (grant No. 945026), internal funds of the Okinawa Institute of Science and Technology Molecular Genetics Unit, the Chan Zuckerberg Biohub Network and the Marthella Foskett Brown Chair in Biological Sciences.
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