Back

Evolutionary Conservation and Divergence of CXCL17 orthologs: Functional Evidence in Reptiles and Loss in the Avian Lineage

Yu, J.; Li, H.-Z.; Wang, J.-J.; Liu, Y.-L.; Guo, Z.-Y.

2026-05-18 biochemistry
10.64898/2026.05.18.725876 bioRxiv
Show abstract

The mucosal chemoattractant C-X-C motif chemokine ligand 17 (CXCL17) was recently identified as a ligand for the orphan G protein-coupled receptor 25 (GPR25). Although CXCL17 orthologs have been identified in fishes, amphibians, and mammals, their presence in reptiles and birds remains unclear. In this study, we employed bioinformatic searches based on gene synteny and sequence features to identify CXCL17 orthologs in public databases. We identified functional CXCL17 orthologs in 46 reptilian species, including lizards, snakes, turtles, and alligators. In contrast, we found only non-functional gene relics in 22 bird species, suggesting the avian lineage lost functional CXCL17 during evolution. A recombinant reptilian CXCL17 from the loggerhead turtle (Caretta caretta), termed Cc-CXCL17, directly bound to and efficiently activated its corresponding receptor, Cc-GPR25, in a C-terminal fragment-dependent manner. Activation of Cc-GPR25 by Cc-CXCL17 also induced chemotactic movement of transfected human embryonic kidney (HEK) 293T cells. In cross-species activity assays, CXCL17s from human and tropical clawed frog could activate Cc-GPR25 albeit with lower potency, but fish orthologs lacked this activity; all tested CXCL17s had no detectable activity towards chicken GPR25, but Cc-CXCL17 had low activity towards mallard GPR25. Our findings demonstrate the presence of functional CXCL17 orthologs in extant reptiles and provide evidence for their evolutionary loss in birds, offering new insights into the phylogenetic distribution of the newly identified CXCL17-GPR25 signaling system.

Matching journals

The top 5 journals account for 50% of the predicted probability mass.

1
Scientific Reports
3102 papers in training set
Top 1%
17.2%
2
eLife
5422 papers in training set
Top 3%
14.1%
3
PLOS Biology
408 papers in training set
Top 0.3%
9.9%
4
PLOS ONE
4510 papers in training set
Top 25%
6.7%
5
Nature Communications
4913 papers in training set
Top 31%
6.2%
50% of probability mass above
6
Communications Biology
886 papers in training set
Top 1.0%
4.2%
7
Cell Reports
1338 papers in training set
Top 17%
3.0%
8
Frontiers in Physiology
93 papers in training set
Top 2%
2.3%
9
Frontiers in Endocrinology
53 papers in training set
Top 1.0%
1.9%
10
BMC Genomics
328 papers in training set
Top 2%
1.9%
11
iScience
1063 papers in training set
Top 12%
1.9%
12
Genome Biology and Evolution
280 papers in training set
Top 1%
1.5%
13
Open Biology
95 papers in training set
Top 1.0%
1.3%
14
Biochemical and Biophysical Research Communications
78 papers in training set
Top 0.8%
1.3%
15
International Journal of Molecular Sciences
453 papers in training set
Top 12%
0.9%
16
Journal of Biological Chemistry
641 papers in training set
Top 3%
0.9%
17
Philosophical Transactions of the Royal Society B
51 papers in training set
Top 5%
0.9%
18
Frontiers in Cell and Developmental Biology
218 papers in training set
Top 8%
0.8%
19
Biomolecules
95 papers in training set
Top 2%
0.8%
20
Royal Society Open Science
193 papers in training set
Top 5%
0.7%
21
Disease Models & Mechanisms
119 papers in training set
Top 3%
0.7%
22
Biochimie
23 papers in training set
Top 0.4%
0.7%
23
Molecular Neurobiology
50 papers in training set
Top 1%
0.7%
24
Cell Communication and Signaling
35 papers in training set
Top 1%
0.7%
25
PeerJ
261 papers in training set
Top 16%
0.7%
26
BMC Biology
248 papers in training set
Top 5%
0.7%
27
Archives of Biochemistry and Biophysics
11 papers in training set
Top 0.2%
0.6%
28
The Journal of Immunology
146 papers in training set
Top 2%
0.6%
29
Nature Ecology & Evolution
113 papers in training set
Top 5%
0.6%
30
Viruses
318 papers in training set
Top 6%
0.6%