# 研究Y染色體的科學家原本預期會發現基因流失的紀錄。 *biotech · news · 2026-06-10 · Earth.com* ## Key points - 研究人員發現一個基因Phf8y，移動並在鹿鼠的Y染色體上複製。 - 這是首個已知基因完整移入哺乳動物Y染色體的例子。 - Phf8y利用跳躍基因機制在Y染色體上轉移並增殖，抵銷其退化趨勢。 - 此發現挑戰了Y染色體只會流失基因、無法獲得新基因的假設。 - Phf8y可能參與精子DNA包裝，潛在影響性別比例及Y染色體演化。 Scientists who study the Y chromosome expect to find a record of loss. Across every mammal studied, the Y sheds genes over millions of years while gaining nothing new. That one-directional picture has been the field’s working assumption. Then, a research team studying deer mice found a gene that seemed to break the rule. The gene had arrived on the Y, copied itself, and built something new on a chromosome the field had written off as a dead end. A shrinking sex chromosome Chromosomes usually travel in matching pairs that swap pieces of DNA, upkeep that catches copying errors before they stick. The Y has no real partner to trade with, so damage builds and its genes wear away, one gene at a time. Even so, the chromosome earns its keep. The genes still hanging on are the ones that build sperm, which makes the Y essential for male fertility. That reputation for slow loss is what a team led by Ivan F. Mier set out to test in deer mice. The research was conducted in the genetics lab of Dr. Jacob Mueller at the University of Michigan Medical School. The backup gene problem Making sperm puts the sex chromosomes in a bind. Partway through, the cell switches the X and Y almost fully off, silencing their genes right when some are needed. Females carry two X chromosomes, so one can cover for the other. Males have just one, with no spare. Evolution leaned on a workaround – copying key X genes onto chromosomes that stay on. Those copies act as backups, and one study traced a copied gene mammals genuinely need for sperm, filling in for an X gene that falls silent. “It’s like having your own clone around who can jump in when you’ve gone on vacation,” said Mier. A gene that jumped In the deer mouse, the team followed a gene that had taken a bizarre route. It began as a routine X chromosome gene called Phf8. From there, it spun off a copy onto an autosome – a chromosome with no part in sex. Then, another copy made it to the Y. On the Y, that lone copy did the unexpected. It duplicated over and over until it formed a small family of near-identical genes, which the team named Phf8y. A gene moving from the X to an autosome is common; biologists have logged many such backups. But no one had recorded a gene finishing the whole journey onto the Y. Not once. “To our knowledge, it is the first example ever,” said Mier. That direction of travel stunned the team. The Y is the chromosome that loses genes, not one that gathers fresh families of them. Watching it take on Phf8y and copy it looked like the reverse of decay. Hijacking the copy machinery Moving a gene between chromosomes takes machinery, and the deer mouse genome had it. Scattered through the DNA of almost every animal are sequences called jumping genes that copy and paste themselves around, making up roughly half of human DNA. Phf8y appears to have exploited exactly that. Rather than the usual path, the gene apparently hijacked this mobile machinery to spin off an extra copy and drop it on the Y. Most of the time these sequences stay quiet, reined in so they cannot reshuffle the genome. Now and then, one breaks free. That rare event apparently handed the Y a whole new gene family. A competitive edge What Phf8y actually does inside the cell is still an open question, even though the team can clearly see it switch on in developing sperm. Everything past that point is informed guesswork. Their best guess is about how DNA gets packed. As a sperm cell matures, its DNA is wound down and crammed into a head far smaller than a normal cell’s. Phf8y may help with that squeeze. Such a role would make sense given where the gene sits. The sex chromosomes are oddly crowded with genes active only in forming sperm, a pattern one analysis of mouse germ cells mapped. House mice hint at why such a gene persists, where rival X and Y genes compete over whether offspring come out male or female. If Phf8y tweaks how sperm carrying the Y are built, it could give them a slight head start. What the discovery means Before this work, the Y chromosome’s story ran one way, toward loss. Phf8y shows traffic can run the other way, a gene completing a full move onto the Y and multiplying after it lands. The dead-end chromosome can build. This discovery changes how biologists understand the Y’s evolution. How new genes reach the Y feeds into how a population keeps a steady sex ratio, near half male and half female. A separate paper that switched off mouse Y genes one by one watched sperm production stumble. For scientists, the finding offers a concrete grip on an old puzzle, why the sexes stay roughly balanced generation after generation. A chromosome long written off as a site of decay is quietly gaining new parts. That gives the field solid ground to work from. The study is published in the journal Current Biology. —– Like what you read? Subscribe to our newsletter for engaging articles, exclusive content, and the latest updates. Check us out on EarthSnap, a free app brought to you by Eric Ralls and Earth.com. —– **Countries:** United States [Read the full story on Earth.com](https://www.earth.com/news/y-chromosome-surprises-scientists-by-gaining-a-new-gene-family/) --- Canonical: https://newsio.io/zh-TW/n/2220deea-2bfc-4327-b7f1-e6d86e439a46/yy Summarized by Newsio from Earth.com. https://newsio.io/how-it-works