TY - JOUR
T1 - Island-specific evolution of a sex-primed autosome in a sexual planarian
AU - Guo, Longhua
AU - Bloom, Joshua S.
AU - Dols-Serrate, Daniel
AU - Boocock, James
AU - Ben-David, Eyal
AU - Schubert, Olga T.
AU - Kozuma, Kaiya
AU - Ho, Katarina
AU - Warda, Emily
AU - Chui, Clarice
AU - Wei, Yubao
AU - Leighton, Daniel
AU - Lemus Vergara, Tzitziki
AU - Riutort, Marta
AU - Sánchez Alvarado, Alejandro
AU - Kruglyak, Leonid
N1 - Publisher Copyright:
© 2022, The Author(s).
PY - 2022/6/9
Y1 - 2022/6/9
N2 - The sexual strain of the planarian Schmidtea mediterranea, indigenous to Tunisia and several Mediterranean islands, is a hermaphrodite1,2. Here we isolate individual chromosomes and use sequencing, Hi-C3,4 and linkage mapping to assemble a chromosome-scale genome reference. The linkage map reveals an extremely low rate of recombination on chromosome 1. We confirm suppression of recombination on chromosome 1 by genotyping individual sperm cells and oocytes. We show that previously identified genomic regions that maintain heterozygosity even after prolonged inbreeding make up essentially all of chromosome 1. Genome sequencing of individuals isolated in the wild indicates that this phenomenon has evolved specifically in populations from Sardinia and Corsica. We find that most known master regulators5–13 of the reproductive system are located on chromosome 1. We used RNA interference14,15 to knock down a gene with haplotype-biased expression, which led to the formation of a more pronounced female mating organ. On the basis of these observations, we propose that chromosome 1 is a sex-primed autosome primed for evolution into a sex chromosome.
AB - The sexual strain of the planarian Schmidtea mediterranea, indigenous to Tunisia and several Mediterranean islands, is a hermaphrodite1,2. Here we isolate individual chromosomes and use sequencing, Hi-C3,4 and linkage mapping to assemble a chromosome-scale genome reference. The linkage map reveals an extremely low rate of recombination on chromosome 1. We confirm suppression of recombination on chromosome 1 by genotyping individual sperm cells and oocytes. We show that previously identified genomic regions that maintain heterozygosity even after prolonged inbreeding make up essentially all of chromosome 1. Genome sequencing of individuals isolated in the wild indicates that this phenomenon has evolved specifically in populations from Sardinia and Corsica. We find that most known master regulators5–13 of the reproductive system are located on chromosome 1. We used RNA interference14,15 to knock down a gene with haplotype-biased expression, which led to the formation of a more pronounced female mating organ. On the basis of these observations, we propose that chromosome 1 is a sex-primed autosome primed for evolution into a sex chromosome.
UR - http://www.scopus.com/inward/record.url?scp=85131295052&partnerID=8YFLogxK
U2 - 10.1038/s41586-022-04757-3
DO - 10.1038/s41586-022-04757-3
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C2 - 35650439
AN - SCOPUS:85131295052
SN - 0028-0836
VL - 606
SP - 329
EP - 334
JO - Nature
JF - Nature
IS - 7913
ER -