Szenker-Ravi Emmanuelle, Ott Tim, Yusof Amirah, Chopra Maya, Khatoo Muznah, Pak Beatrice, Xuan Goh Wei, Beckers Anja, Brady Angela F, Ewans Lisa J, Djaziri Nabila, Almontashiri Naif A M, Alghamdi Malak Ali, Alharby Essa, Dasouki Majed, Romo Lindsay, Tan Wen-Hann, Maddirevula Sateesh, Alkuraya Fowzan S, Giordano Jessica L, Alkelai Anna, Wapner Ronald J, Stals Karen, Alfadhel Majid, Alswaid Abdulrahman Faiz, Bogusch Susanne, Schafer-Kosulya Anna, Vogel Sebastian, Vick Philipp, Schweickert Axel, Wakeling Matthew, Moreau de Bellaing Anne, Alshamsi Aisha M, Sanlaville Damien, Mbarek Hamdi, Saad Chadi, Ellard Sian, Eisenhaber Frank, Tripolszki Kornelia, Beetz Christian, Bauer Peter, Gossler Achim, Eisenhaber Birgit, Blum Martin, Bouvagnet Patrice, Bertoli-Avella Aida, Amiel Jeanne, Gordon Christopher T, Reversade Bruno
Laboratory of Human Genetics & Therapeutics, Genome Institute of Singapore (GIS), A(∗)STAR, Singapore, Singapore; Laboratory of Human Genetics & Therapeutics, BESE, KAUST, Thuwal, Saudi Arabia.
Institute of Biology, University of Hohenheim, Garbenstr. 30, 70599 Stuttgart, Germany.
Am J Hum Genet. 2025 Feb 6;112(2):353-373. doi: 10.1016/j.ajhg.2024.12.006. Epub 2025 Jan 2.
Four genes-DAND5, PKD1L1, MMP21, and CIROP-form a genetic module that has specifically evolved in vertebrate species that harbor motile cilia in their left-right organizer (LRO). We find here that CIROZ (previously known as C1orf127) is also specifically expressed in the LRO of mice, frogs, and fish, where it encodes a protein with a signal peptide followed by 3 zona pellucida N domains, consistent with extracellular localization. We report 16 individuals from 10 families with bi-allelic CIROZ inactivation variants, which cause heterotaxy with congenital heart defects. While the knockout of Ciroz in mice also leads to situs anomalies, we unexpectedly find that its targeted inactivation in zebrafish and Xenopus does not lead to observable LR anomalies. Moreover, CIROZ is absent or obsolete in select animals with motile cilia at their LRO, including Carnivora, Atherinomorpha fish, or jawless vertebrates. In summary, this evo-devo study identifies CIROZ as an essential gene for breaking bilateral embryonic symmetry in humans and mice, whereas we witness its contemporary pseudogenization in discrete vertebrate species.
四个基因——DAND5、PKD1L1、MMP21和CIROP——形成了一个基因模块,该模块在其左右组织者(LRO)中具有活动纤毛的脊椎动物物种中特异性进化。我们在此发现,CIROZ(以前称为C1orf127)也在小鼠、青蛙和鱼类的LRO中特异性表达,在那里它编码一种带有信号肽的蛋白质,后面跟着3个透明带N结构域,这与细胞外定位一致。我们报告了来自10个家庭的16名个体,他们携带双等位基因CIROZ失活变体,这些变体会导致伴有先天性心脏缺陷的内脏反位。虽然在小鼠中敲除Ciroz也会导致位置异常,但我们意外地发现,在斑马鱼和非洲爪蟾中对其进行靶向失活不会导致可观察到的左右异常。此外,在其LRO中具有活动纤毛的某些动物中,包括食肉动物、银汉鱼目鱼类或无颌脊椎动物,CIROZ不存在或已过时。总之,这项进化发育研究将CIROZ确定为人类和小鼠打破双侧胚胎对称性的必需基因,而我们在离散的脊椎动物物种中见证了它当代的假基因化。