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身為一個熱愛美食、喜歡在城市裡挖掘驚喜的人,臺中公益路一直是我最常出沒的地方之一。這條路可說是「臺中人的美食戰場」,從精緻西餐到創意火鍋,從日式丼飯到義式早午餐,每走幾步,就會有完全不同的特色料理餐廳。 這次我特別花了一整個月,實際造訪了公益路上十間口碑不錯的餐廳。有的是網友熱推的打卡名店,也有隱藏在巷弄裡的小驚喜。我以環境氛圍、口味表現、價格CP值與再訪意願為基準,整理出這篇實測評比。希望能幫正在猶豫去哪裡吃飯的你,找到那一間「吃完會想再來」的餐廳。 評比標準與整理方向
這次我走訪的10家餐廳橫跨不同料理類型,從高質感牛排館到巷弄系早午餐,每一間都有自己獨特的風格。為了讓整體比較更客觀,我依照以下四大面向進行評比,並搭配實際用餐體驗來打分。
整體而言,我希望這份評比不只是「哪家好吃」,而是幫你在不同情境下(約會、家庭聚餐、朋友小聚、商業午餐)都能快速找到合適的選擇。畢竟,美食不只是味覺的滿足,更是一段段與朋友共享的生活記憶。 10間臺中公益路餐廳評比懶人包公益路向來是臺中人聚餐的首選地段,從火鍋、燒肉到中式料理與早午餐,每走幾步就有驚喜。以下是我實際造訪過的10間代表性餐廳清單,橫跨平價、創意、高級各路風格。
一頭牛日式燒肉|炭香濃郁的和牛饗宴,約會聚餐首選
走在公益路上,很難不被 一頭牛日式燒肉 的木質外觀吸引。低調卻不失質感的門面,搭配昏黃燈光與暖色調的內裝,讓人一進門就感受到濃濃的日式職人氛圍。店內空間不大,但桌距規劃得宜,每桌皆設有獨立排煙設備,烤肉時完全不怕滿身油煙味。 餐點特色
一頭牛的靈魂,絕對是他們招牌的「三國和牛拼盤」。 用餐體驗整體節奏掌握得非常好。店員會在你剛想烤下一片肉時貼心遞上夾子、幫忙換烤網,讓人完全不用分心。整場用餐過程就像一場表演,從視覺、嗅覺到味覺都被滿足。 綜合評分
地址:408臺中市南屯區公益路二段162號電話:04-23206800 官網:http://www.marihuana.com.tw/yakiniku/index.html 小結語一頭牛日式燒肉不僅是「吃肉的地方」,更像是一場五感盛宴。從進門那一刻到最後一道甜點,都能感受到他們對細節的用心。 TANG Zhan 湯棧|文青系火鍋代表,麻香湯底與視覺美感並重
在公益路這條美食戰線上,TANG Zhan 湯棧 是讓人一眼就會想走進去的那一種。 餐點特色
湯棧最有名的當然是它的「麻香鍋」。 用餐體驗整體氛圍比一般火鍋店更有質感。 綜合評分
地址:408臺中市南屯區公益路二段248號電話:04-22580617 官網:https://www.facebook.com/TangZhan.tw/ 小結語TANG Zhan 湯棧 把傳統火鍋做出新的樣貌保留臺式鍋物的溫度,又結合現代風格與細節服務,讓吃鍋這件事變得更有品味。 如果你想找一間兼具「好吃、好拍、好放鬆」的火鍋店,湯棧會是公益路上最有風格的選擇之一。 NINI 尼尼臺中店|明亮寬敞的義式早午餐天堂
如果說前兩間是肉食愛好者的天堂,那 NINI 尼尼臺中店 絕對是想放鬆、聊聊天的好地方。餐廳外觀以白色系與大片玻璃窗為主,陽光灑進室內,讓人一踏入就有種度假般的輕盈感。假日早午餐時段特別熱鬧,建議提早訂位。 餐點特色
NINI 的菜單融合義式與臺灣人口味,選擇多樣且份量十足。主打的 松露燉飯 濃郁卻不膩口,米芯保留微Q口感;而 香蒜海鮮義大利麵 則以新鮮白蝦、花枝與淡菜搭配微辣蒜香,口感層次豐富。 用餐體驗店內氣氛輕鬆不拘謹,無論是一個人帶電腦工作、或朋友聚餐,都能找到舒服角落。餐點上桌速度穩定,服務人員態度親切、補水與收盤都非常主動。整體節奏讓人覺得「時間變慢了」,很適合想遠離忙碌日常的人。 綜合評分
地址:40861臺中市南屯區公益路二段18號電話:04-23288498 小結語NINI 尼尼臺中店是一間能讓人放下手機、慢慢吃飯的餐廳。餐點不追求浮誇,而是以「剛剛好」的份量與風味,陪伴每個平凡午後。如果你在找一間能邊吃邊聊天、拍照也漂亮的早午餐店,NINI 會是你在公益路上最不費力的幸福選擇。 加分100%浜中特選昆布鍋物|平價卻用心的湯頭系火鍋,家庭聚餐好選擇
在公益路這條高質感餐廳林立的戰場上,加分100%浜中特選昆布鍋物 走的是截然不同的路線。它沒有浮誇的裝潢、也沒有高價位的套餐,但靠著實在的湯頭與親切的服務,默默吸引許多回頭客。每到用餐時間,總能看到家庭或情侶三兩成群地圍著鍋邊聊天。 餐點特色
主打 北海道浜中昆布湯底,湯頭清澈卻不單薄,越煮越能喝出海藻與柴魚的自然香氣。 用餐體驗整體氛圍偏家庭取向,桌距寬敞、座位舒適,帶小孩來也不覺擁擠。店員態度親切,補湯、收盤都很勤快,給人一種「被照顧著」的安心感。 綜合評分
地址:403臺中市西區公益路288號電話:0910855180 小結語加分100%浜中特選昆布鍋物是一間「不浮誇、但會讓人想再訪」的火鍋店。它不追求豪華擺盤,而是用最簡單的湯頭與新鮮食材,傳遞出家常卻不平凡的溫度。 印月餐廳|中式料理的藝術演繹,宴客與家庭聚會首選
說到臺中公益路的中式料理代表,印月餐廳 絕對是榜上有名。這間開業多年的餐廳以「中菜西吃」的概念聞名,把傳統中式料理以現代手法重新詮釋。從建築外觀到餐具擺設,每個細節都散發著低調的典雅氣息。 餐點特色
印月最令人印象深刻的是他們將傳統中菜融入創意手法。 用餐體驗服務方面完全對得起餐廳的高級定位。從入座、點餐到上菜節奏,都拿捏得恰如其分。每道菜都會有服務人員細心介紹食材與吃法,讓人感受到「被款待」的尊榮感。 綜合評分
地址:408臺中市南屯區公益路二段818號電話:0422511155 小結語印月餐廳是一間「不只吃飯,更像品味生活」的地方。 KoDō 和牛燒肉|極致職人精神,專為儀式感與頂級味覺而生
若要形容 KoDō 和牛燒肉 的用餐體驗,一句話足以總結——「像在欣賞一場關於肉的表演」。 餐點特色
這裡主打 日本A5和牛冷藏肉,以「精切厚燒」的方式呈現。 用餐體驗KoDō 的最大特色是「儀式感」。 綜合評分
地址:403臺中市西區公益路260號電話:0423220312 官網:https://www.facebook.com/kodo2018/ 小結語KoDō 和牛燒肉不是日常餐廳,而是一場體驗。 永心鳳茶|在茶香裡用餐的優雅時光,臺味早午餐的新詮釋
走進 永心鳳茶公益店,彷彿進入一間有氣質的茶館。 餐點特色
永心鳳茶的餐點結合中式靈魂與西式擺盤,無論是「炸雞腿飯」還是「紅玉紅茶拿鐵」,都能讓人感受到熟悉卻不平凡的味道。 用餐體驗店內服務人員態度溫和,對茶品介紹詳盡。上餐節奏剛好,不急不徐。 綜合評分
地址:40360臺中市西區公益路68號三樓(勤美誠品)電話:0423221118 小結語永心鳳茶讓人重新定義「臺味」。 三希樓|老饕級江浙功夫菜,穩重又帶人情味的中式饗宴
位於公益路上的 三希樓 是許多臺中老饕的口袋名單。 餐點特色
三希樓的菜色以 江浙與港式料理 為主,兼顧傳統與現代風味。 用餐體驗三希樓的服務給人一種老派但貼心的感覺。 綜合評分
地址:408臺中市南屯區公益路二段95號電話:0423202322 官網:https://www.sanxilou.com.tw/ 小結語三希樓是一間「吃得出功夫」的餐廳。 一笈壽司|低調奢華的無菜單日料,職人手藝詮釋旬味極致
在熱鬧的公益路上,一笈壽司 低調得幾乎不顯眼。 餐點特色
一笈壽司採 Omakase(無菜單料理) 形式,每一餐都由主廚根據當日食材設計。 用餐體驗整場用餐約90分鐘,節奏緩慢但沉穩。 綜合評分
地址:408臺中市南屯區公益路二段25號電話:0423206368 官網:https://www.facebook.com/YIJI.sushi/ 小結語一笈壽司是一間真正讓人「放慢呼吸」的餐廳。 茶六燒肉堂|人氣爆棚的和牛燒肉聖地,肉香與幸福感同時滿分
若要票選公益路上「最難訂位」的餐廳,茶六燒肉堂 絕對名列前茅。 餐點特色
茶六主打 和牛燒肉套餐,價格約落在 $700–$1000 間,份量與品質兼具。 用餐體驗茶六的服務效率相當高。店員親切、換網勤快、補水速度快,整場用餐流程流暢無壓力。 綜合評分
地址:403臺中市西區公益路268號電話:0423281167 官網:https://inline.app/booking/-L93VSXuz8o86ahWDRg0:inline-live-karuizawa/-LUYUEIOYwa7GCUpAFWA 小結語茶六燒肉堂用「穩定品質+輕奢氛圍」抓住了臺中年輕族群的心。 吃完10家公益路餐廳後的心得與結語吃完這十家餐廳後,臺中公益路不只是一條美食街,而是一段生活風景線。 有的餐廳講究細膩與儀式感,像 一頭牛日式燒肉 與 一笈壽司,讓人感受到食材最純粹的美好 有的則以親切與溫度打動人心,像 加分昆布鍋物、永心鳳茶,讓人明白吃飯不只是為了飽足,而是一種被照顧的幸福。 而像茶六燒肉堂、TANG Zhan 湯棧 這類人氣名店,則用穩定的品質與熱絡的氛圍,成為許多臺中人心中「想吃肉就去那裡」的代名詞。 這十家店,構成了公益路最動人的縮影 有華麗的,也有溫柔的;有傳統的,也有創新的。 每一家都在自己的風格裡發光,讓人吃到的不只是料理,而是一種生活的溫度與節奏。 對我而言,這不僅是一場美食旅程,更是一趟關於「臺中味道」的回憶之旅。 FAQ:關於臺中公益路美食常見問題Q1:公益路哪一區的餐廳最集中? Q2:需要提前訂位嗎? 最後的話若要用一句話形容這趟美食之旅,我會說: 一笈壽司套餐劃算嗎? 如果你也和我一樣喜歡用味蕾探索一座城市,那就把這篇公益路美食攻略收藏起來吧。TANG Zhan 湯棧長輩會喜歡嗎? 無論是約會、慶生、家庭聚餐,或只是想犒賞一下辛苦的自己——這條路上永遠會有一間剛剛好的餐廳在等你。印月餐廳用餐時間會不會太短? 下一餐,不妨從這10家開始。TANG Zhan 湯棧過年期間會開門嗎? 打開手機、約上朋友,讓公益路成為你生活裡最容易抵達的小確幸。加分100%浜中特選昆布鍋物第一次來要點什麼? 如果你有私心愛店,也歡迎留言分享,加分100%浜中特選昆布鍋物長輩會喜歡嗎? 你的推薦,可能讓我下一趟美食旅程變得更精彩。NINI 尼尼臺中店年節期間價格會變嗎? Research suggests that all complex life forms, including humans, plants, and animals, trace their roots to a common Asgard archaean ancestor. This discovery aids in understanding the evolutionary step from microbes to eukaryotes and reveals that the Asgard archaea, evolving over 2 billion years ago, appear to be the progenitors of eukaryotic organisms. Scientists have traced the origins of all complex life to Asgard archaea, ancient microbes that include our closest evolutionary relatives. Genetic evidence suggests that these microorganisms developed traits that paved the way for eukaryotic life, revealing a crucial step in life’s evolution. The mythological Norse god Thor hails from the celestial city of Asgard, and according to revolutionary research published in the scientific journal, Nature, he’s not the only Asgardian. This new research suggests that we humans — along with eagles, starfish, daisies, and every complex organism on Earth — are, in a sense, Asgardians. The research team at The University of Texas at Austin, along with collaborators from different institutions, conducted a genomic analysis of several hundreds of microorganisms known as archaea. Their findings revealed that eukaryotes – complex life forms with nuclei in their cells, including all flora, fauna, insects, and fungi across the globe – can trace their origins back to a common Asgard archaean ancestor. A Common Ancestor for Complex Life That means eukaryotes are, in the parlance of evolutionary biologists, a “well-nested clade” within Asgard archaea, similar to how birds are one of several groups within a larger group called dinosaurs, sharing a common ancestor. The team has found that all eukaryotes share a common ancestor among the Asgards. According to this latest study, all complex life forms (a.k.a. eukaryotes) trace their roots back to a common ancestor among a group of microbes called the Asgard archaea. Credit: University of Texas at Austin No fossils of eukaryotes have been found from farther back than about 2 billion years ago, suggesting that before that, only various types of microbes existed. “So, what events led microbes to evolve into eukaryotes?” said Brett Baker, UT Austin associate professor of integrative biology and marine science. “That’s a big question. Having this common ancestor is a big step in understanding that.” Led by Thijs Ettema of Wageningen University in the Netherlands, the research team identified the closest microbial relative to all complex life forms on the tree of life as a newly described order called the Hodarchaeales (or Hods for short). The Hods, found in marine sediments, are one of several subgroups within the larger group of Asgard archaea. The Asgard archaea evolved more than 2 billion years ago, and their descendants are still living. Some have been discovered in deep-sea sediments and hot springs around the world, but so far only two strains have been successfully grown in the lab. To identify them, scientists collect their genetic material from the environment and then piece together their genomes. Based on genetic similarities with other organisms that can be grown in the lab and studied, the scientists can infer metabolism and other features of the Asgards. Reconstructing the Dawn of Complex Life “Imagine a time machine, not to explore the realms of dinosaurs or ancient civilizations, but to journey deep into the potential metabolic reactions that could have sparked the dawn of complex life,” said Valerie De Anda, a researcher in Baker’s lab. “Instead of fossils or ancient artifacts, we look at the genetic blueprints of modern microbes to reconstruct their past.” Some of the microbes analyzed for this study were collected using the Alvin deep-sea submersible, seen here on a collection trip in the Guaymas Basin in November 2018. Credit: Brett Baker The researchers expanded the known Asgard genomic diversity, adding more than 50 undescribed Asgard genomes as input for their modeling. Their analysis indicates that the ancestor of all modern Asgards appears to have been living in hot environments, consuming CO2 and chemicals to live. Meanwhile, Hods, which are more closely related to eukaryotes, are metabolically more similar to us, eating carbon and living in cooler environments. “This is really exciting because we are looking for the first time at the molecular blueprints of the ancestor that gave rise to the first eukaryotic cells,” De Anda said. In Norse mythology, Hod (also spelled Höd, Höðr or Hoder) is a god, the blind son of Odin and Frigg, who is tricked into killing his own brother Baldr. “I keep joking in my talks that ‘We are all Asgardian’,” Baker said. “Now that’s probably going to be on my tombstone.” Asgard archaea tree. Credit: University of Texas at Austin “To me, the most exciting thing is that we’re starting to see the transition from what biologists think is an archaeon to this organism Hodarchaeales that is more like a eukaryote,” Baker explained. “Another way to put it is that these Hods are our sister group in the archaeal world.” How Gene Duplication Drove Evolution Baker said it makes sense that of all the archaea, the Asgards are the ones that spawned eukaryotes. Like eukaryotes, members of the Asgard archaea have many genes with multiple copies in their genomes. In eukaryotes, when genes became duplicated, the new copies often took on new functions, giving organisms new abilities. It was one of the big drivers of evolution. “We don’t know, in these Asgards specifically, what the gene duplications led to,” Baker said. “But we know in eukaryotes that gene duplications led to new functions and an increasing of cellular complexity. So, we think that that’s one of the ways that Asgards led to the innovations that define eukaryotes.” Scientists studying archaea have found many proteins that were once thought to be exclusive to eukaryotes. Baker said that raises the question: What functions are these eukaryotic proteins serving in the archaea? “I think studying these simpler forms of life and their eukaryotic characteristics is going to tell us a lot about ourselves,” Baker said. Reference: “Inference and reconstruction of the heimdallarchaeial ancestry of eukaryotes” by Laura Eme, Daniel Tamarit, Eva F. Caceres, Courtney W. Stairs, Valerie De Anda, Max E. Schön, Kiley W. Seitz, Nina Dombrowski, William H. Lewis, Felix Homa, Jimmy H. Saw, Jonathan Lombard, Takuro Nunoura, Wen-Jun Li, Zheng-Shuang Hua, Lin-Xing Chen, Jillian F. Banfield, Emily St John, Anna-Louise Reysenbach, Matthew B. Stott, Andreas Schramm, Kasper U. Kjeldsen, Andreas P. Teske, Brett J. Baker and Thijs J. G. Ettema, 14 June 2023, Nature. DOI: 10.1038/s41586-023-06186-2 Support for this research was provided by the Origin of Eukaryotes program at the Moore and Simons Foundations, U.S. National Science Foundation, the Wellcome Trust Foundation, the European Research Council, the Swedish Research Council, the Dutch Research Council, the National Natural Science Foundation of China, the Wenner-Gren Foundation, the Science for Life Laboratory (Sweden) and the European Commission’s Marie Skłodowska-Curie Actions. Other authors from UT Austin are Kiley W. Seitz and Nina Dombrowski. In addition to Ettema, authors from other institutions are Laura Eme, Daniel Tamarit, Eva Caceres, Courtney Stairs, Max Schön, William Lewis, Felix Homa, Jimmy Saw, Jonathan Lombard, Takuro Nunoura, Wen-Jun Li, Zheng-Shuang Hua, Lin-Xing Chen, Jillian Banfield, Emily St. John, Anna-Louise Reysenbach, Matthew Stott, Andreas Schramm, Kasper Kjeldsen and Andreas Teske. A new study reveals a key group of neurons responsible for controlling left-right movements, offering insights that could benefit Parkinson’s disease treatment. This discovery highlights the complex interaction between the brainstem and basal ganglia in movement control. Scientists have identified a group of brain cells in mice that facilitate their ability to turn right or left. This finding could potentially be applied in future treatments for Parkinson’s disease. Have you ever wondered what happens in the brain when we move to the right or left? Most people don’t; they simply perform these movements automatically. However, this seemingly straightforward action is governed by a complex process. In a new study, researchers have discovered the missing piece in the complex nerve-network needed for left-right turns. The discovery was made by a research team consisting of Assistant Professor Jared Cregg, Professor Ole Kiehn, and their colleagues from the Department of Neuroscience at the University of Copenhagen. In 2020, Ole Kiehn, Jared Cregg, and their colleagues identified the ‘brain’s steering wheel’ – a network of neurons in the lower part of the brainstem that commands right- and left- movements when walking. At the time, though, it was not clear to them how this right-left circuit is controlled by other parts of the brain, such as the basal ganglia. The Connection to Basal Ganglia “We have now discovered a new group of neurons in the brainstem which receives information directly from the basal ganglia and control the right-left circuit,” Ole Kiehn explains. Eventually, this discovery may be able to help people suffering from Parkinson’s disease. The study has been published in the esteemed scientific journal Nature Neuroscience. The basal ganglia are located deep within the brain. For many years now, they have been known to play a key role in controlling voluntary movements. Years ago, scientists learned that by stimulating the basal ganglia you can affect right- and left-hand movements in mice. They just did not know how. “When walking, you will shorten the step length of the right leg before making a right-hand turn and the left leg before making a left-hand turn. The newly discovered network of neurons is located in a part of the brainstem known as PnO. They are the ones that receive signals from the basal ganglia and adjust the step length as we make a turn, and which thus determine whether we move to the right or left,” Jared Cregg explains. The study therefore provides a key to understanding how these absolutely essential movements are produced by the brain. In the new study, the researchers studied the brain of mice, as their brainstem closely resembles the human brainstem. Therefore, the researchers expect to find a similar right-left circuit in the human brain. People with Parkinson’s have difficulties making right and left turns Parkinson’s disease is caused by a lack of dopamine in the brain. This affects the basal ganglia, and the researchers responsible for the new study believe that this leads to failure to activate the brainstem’s right-left circuit. And it makes sense when you look at the symptoms experienced by people with Parkinson’s at a late stage of the disease – they often have difficulties turning when walking. In the new study, the researchers have studied this in mice with symptoms resembling those of people with Parkinson’s disease. They made the so-called Parkinson’s model, removing dopamine from the brain of mice and thus giving them motor symptoms similar to those experienced by people suffering from Parkinson’s disease “These mice had difficulties turning, but by stimulating the PnO neurons we were able to alleviate turning difficulties,” Jared Cregg says. Using Deep Brain Stimulation, scientists may eventually be able to develop similar stimulation for humans. At present, though, they are unable to stimulate human brain cells as accurately as in mice models, where they used advanced optogenetic techniques. “The neurons in the brainstem are a mess, and electric stimulation, which is the type of stimulation used in human Deep Brain Stimulation, cannot distinguish the cells from one another. However, our knowledge of the brain is constantly growing, and eventually, we may be able to start considering focused Deep Brain Stimulation of humans,” Ole Kiehn concludes. Reference: “Basal ganglia–spinal cord pathway that commands locomotor gait asymmetries in mice” by Jared M. Cregg, Simrandeep K. Sidhu, Roberto Leiras and Ole Kiehn, 12 February 2024, Nature Neuroscience. DOI: 10.1038/s41593-024-01569-8 Evolution is not just about gaining complexity but often involves gene loss, which can drive new adaptations. The “less, but more” model suggests that losing genes can lead to later expansions, shaping species’ evolution in unexpected ways. Losing Opens Up New Possibilities for Subsequent Gains Evolution is traditionally associated with increasing complexity and the acquisition of new genes. However, the advent of the genomic era has revealed that gene loss and simplification occur far more frequently in species evolution than previously thought. These processes can drive new biological adaptations that enhance the survival of living organisms. This evolutionary mechanism, which may seem counterintuitive—where “less is more” in genetic terms—now unveils a surprising dimension. It aligns with the emerging evolutionary concept of “less, but more,” characterized by massive gene losses followed by extensive expansions through gene duplications. This is one of the main conclusions of an article published in the journal Molecular Biology and Evolution, led by a team from the Genetics Section of the Faculty of Biology and the Institute for Research on Biodiversity (IRBio) of the University of Barcelona, in which teams from the Okinawa Institute of Science and Technology (OIST) have also participated. Using the “less, but more” model, a study by the University of Barcelona identifies how massive gene losses followed by extensive gene duplications can generate evolutionary adaptations in species. Credit: Molecular Biology and Evolution The paper identifies new evolutionary patterns, and it outlines a new scenario, marked by the enormous potential for genetic change and evolutionary adaptation driven by large-scale gene loss and duplication in living organisms. Less, but more: a new evolutionary scenario There are still many questions about the impact of gene loss on the diversification of species and the emergence of evolutionary innovations in the planetary tree of life. “Gene loss is a widespread mechanism throughout the biological scale and represents an evolutionary driving force that can generate genetic variability and also biological adaptations, and this has traditionally been known as the ‘less is more’ hypothesis,” says Cristian Cañestro, leader of the study and member of the UB’s consolidated research group on Evolution and Development (Evo-Devo) of the UB’s Department of Genetics, Microbiology, and Statistics. Now, the new paper describes a new evolutionary framework called “less, but more,” which extends the previous model in terms of the importance of gene loss as an evolutionary driving force. Cristian Cañestro and Gaspar Sánchez-Serna. Credit: UNIVERSITY OF BARCELONA This study, which is part of Gaspar Sánchez-Serna’s doctoral thesis, focuses on the study of the genome of the Oikopleura dioica species, a swimming organism of the marine zooplankton that belongs to the tunicates — a sister group of vertebrates — and is phylogenetically linked to evolutionary history. In this study model — a free-living tunicate or appendicularian — the team reconstructed the evolutionary history of fibroblast growth factor (FGF) gene families, which are critical in the developmental process of organisms. “The findings suggest that the process of gene loss reduced the number of FGF growth factor gene families from eight to just two, which are the Fgf9/16/20 and Fgf11/12/13/14 families. These surviving subfamilies have doubled over the course of evolution to generate a total of ten genes in appendicularians,” explains Sánchez-Serna, first author of the paper. “In particular, Fgf9/16/20 and Fgf11/12/13/14 may represent a minimal set of subfamilies that have conserved secretory and intracellular functions, respectively, and reveal important information about the evolution of the FGF system,” he continues. From sessile life to active swimming The study provides a new perspective on the evolution of FGF subfamilies in the chordate group, with massive losses and duplications of ancestral gene families originating at the base of the appendicular lineage after they diverged from the ascidians. All these changes have contributed to morphological divergence between different species of free-living tunicates, such as O. dioica. “Our study presents a new hypothesis on how FGF gene losses and duplications may be related to developmental changes. We are talking about evolutionary innovations — changes in morphology and body plan, etc. — that drove the evolution from the ascidian-like sessile lifestyle to free-living, actively swimming forms such as appendicularians,” says Sánchez-Serna. The study also identifies differences in the structure of the FGF genes of O. dioica from different parts of the world, providing the first molecular evidence of how these rapidly evolving populations are becoming cryptic species (i.e. consisting of organisms very similar in morphology and genome that have hitherto been classified in the same species). The “less, but more” evolutionary model “helps us to understand how sometimes losing opens up new possibilities for subsequent gains and, therefore, losses are necessary to favor the evolutionary origin of new adaptations,” concludes Cristian Cañestro. Reference: “Less, but More: New Insights From Appendicularians on Chordate Fgf Evolution and the Divergence of Tunicate Lifestyles” by Gaspar Sánchez-Serna, Jordi Badia-Ramentol, Paula Bujosa, Alfonso Ferrández-Roldán, Nuria P Torres-Águila, Marc Fabregà-Torrus, Johannes N Wibisana, Michael J Mansfield, Charles Plessy, Nicholas M Luscombe, Ricard Albalat and Cristian Cañestro, 17 December 2024, Molecular Biology and Evolution. DOI: 10.1093/molbev/msae260 RRG455KLJIEVEWWF 三希樓尾牙拍照效果好嗎? 》公益路美食新手指南|10家必吃推薦KoDō 和牛燒肉氣氛如何? 》台中公益路美食巡禮|10家好吃到想回訪印月餐廳情侶來合適嗎? 》公益路美食最佳選擇|10家餐廳逐一分析 |
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