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Single-cell analysis of the amphioxus hepatic caecum and vertebrate liver reveals genetic mechanisms of vertebrate liver evolution.

Baosheng WuWenjie XuKunjin WuYe LiMing-Liang HuChenguang FengChenglong ZhuJiangmin ZhengXinxin CuiJing LiDeqian FanFenghua ZhangYuxuan LiuJinping ChenChang LiuGuang LiQiang QiuKai QuWen WangKun Wang
Published in: Nature ecology & evolution (2024)
The evolution of the vertebrate liver is a prime example of the evolution of complex organs, yet the driving genetic factors behind it remain unknown. Here we study the evolutionary genetics of liver by comparing the amphioxus hepatic caecum and the vertebrate liver, as well as examining the functional transition within vertebrates. Using in vivo and in vitro experiments, single-cell/nucleus RNA-seq data and gene knockout experiments, we confirm that the amphioxus hepatic caecum and vertebrate liver are homologous organs and show that the emergence of ohnologues from two rounds of whole-genome duplications greatly contributed to the functional complexity of the vertebrate liver. Two ohnologues, kdr and flt4, play an important role in the development of liver sinusoidal endothelial cells. In addition, we found that liver-related functions such as coagulation and bile production evolved in a step-by-step manner, with gene duplicates playing a crucial role. We reconstructed the genetic footprint of the transfer of haem detoxification from the liver to the spleen during vertebrate evolution. Together, these findings challenge the previous hypothesis that organ evolution is primarily driven by regulatory elements, underscoring the importance of gene duplicates in the emergence and diversification of a complex organ.
Keyphrases
  • single cell
  • rna seq
  • genome wide
  • endothelial cells
  • gene expression
  • oxidative stress
  • acute myeloid leukemia
  • electronic health record
  • tyrosine kinase
  • artificial intelligence
  • genome wide analysis