The world's first cloned golden wild yak via interspecific SCNT: 4800m donor origin and 4200m vitrified blastocyst transfer
Dawei YuiD, Qiang Zhang, Lei CaoiD, Shigang Gu, Yurong ZhangiD, Chang Liu, Kangjun Yin, Jing Wang, Bo Pan, Y. L. Liu, Guangbin ZhouiD, Daoliang LaniD, Yongye HuangiD, Wangdui BasangiD
Abstract
Primarily inhabiting the harsh, high-altitude environment of the Qiangtang National Nature Reserve exceeding 5,000 meters above the sea (m.a.s.l.), the golden wild yak is critically endangered, with fewer than 300 individuals remaining in the world, a situation exacerbated by the significant challenges of conducting research and conservation of their genetic resources. Somatic cell nuclear transfer (SCNT) can be an effective method for their preservation, but facing several obstacles in this context, including the hypoxic stress at high altitude that impairs embryonic development due to in vitro manipulation, and constraints of long-distance embryo transport. In the present study, the ear tissue was collected from a childhood male golden wild yak at Xizang Geye Wildlife Rescue Station (4800 m.a.s.l.) and send to Institute of Animal Science at Beijing to derive fibroblast cells. Using fibroblast cells of the golden wild yak as nuclear donors, and bovine oocytes from a local slaughterhouse at Beijing as recipients, the interspecific SCNT (iSCNT) embryos were generated and in vitro developed to blastocysts. To maintain the embryonic viability after long-distance transportation from Beijing to Xizang, iSCNT blastocysts were subjected to cryopreservation by vitrification method. Thawing of vitrified iSCNT blastocysts were completed at Xizang Dangxiong Yak Breeding Innovation Base (4200 m.a.s.l.), and transferred into the uterine horn of domestic yaks. 257 days after blastocyst transfer, a cloned golden wild yak was successfully harvested on January 10, 2026. This work demonstrates, for the first time, that interspecies somatic cell nuclear transfer can successfully produce a cloned offspring under extreme conditions, spanning 4800 m.a.s.l. donor origin, long-distance vitrified embryo transportation, and high-altitude blastocyst transfer at 4200 m.a.s.l., establishing a viable strategy for conserving critically endangered high-altitude species.
02 /Specification & Classification
Click any tag to browse matching papersReproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Hybrid yak-cattle in situ conservation via interspecies somatic cell nuclear transfer at ultra-high-altitude region
Dawei Yu, Qunzong Nima, … Yongye Huang·bioRxiv·Jul 10, 2025
- Endangered Przewalski's horse, Equus przewalskii, cloned from historically cryopreserved cells
Ben J. Novak, Oliver A. Ryder, … Ryan M. Phelan·AnimalsPeer-reviewed·Feb 20, 2025
- First endangered black-footed ferrets, Mustela nigripes, cloned for genetic rescue
Ben J. Novak, Pete Gober, … Ryan M. Phelan·bioRxiv·Apr 17, 2024
- Extreme temperatures impede the release success of captive-bred avian scavengers
Nili Anglister, Marta Acácio, … Orr Spiegel·Ornithological ApplicationsPeer-reviewed·Mar 11, 2026
- Fetal Kidney Transplantation for In Utero Fetuses
Keita Morimoto, Shuichiro Yamanaka, … Takashi Yokoo·Communications BiologyPeer-reviewed·Mar 3, 2025
- Rapid Derivation of Cloning-Competent Cells from Peripheral Blood Advances Conservation Biobanking
Laura Knecht, Anthony Mastracci, … James Kehler·Journal of HeredityPeer-reviewed·Jun 24, 2026