SPECC1L regulates palate development downstream of IRF6. (29th January 2020)

• Record Type: Journal Article
• Authors: Hall, Everett G; Wenger, Luke W; Wilson, Nathan R; Undurty-Akella, Sraavya S; Standley, Jennifer; Augustine-Akpan, Eno-Abasi; Kousa, Youssef A; Acevedo, Diana S; Goering, Jeremy P; Pitstick, Lenore; Natsume, Nagato; Paroya, Shahnawaz M; Busch, Tamara D; Ito, Masaaki; Mori, Akihiro; Imura, Hideto; Schultz-Rogers, Laura E; Klee, Eric W; Babovic-Vuksanovic, Dusica; Kroc, Sarah A; Adeyemo, Wasiu L; Eshete, Mekonen A; Bjork, Bryan C; Suzuki, Satoshi; Murray, Jeffrey C; Schutte, Brian C; Butali, Azeez; Saadi, Irfan
• Is Part Of: Human molecular genetics. Volume 29:Number 5(2020)
• Page Start: 845
• Page End: 858
• Publication Date: 2020-01-29
• Subjects: Human molecular genetics -- Periodicals; Human chromosome abnormalities -- Periodicals; 572.8
• DOI: 10.1093/hmg/ddaa002
• Languages: English
• ISSNs: 0964-6906

Abstract

Abstract: SPECC1L mutations have been identified in patients with rare atypical orofacial clefts and with syndromic cleft lip and/or palate (CL/P). These mutations cluster in the second coiled-coil and calponin homology domains of SPECC1L and severely affect the ability of SPECC1L to associate with microtubules. We previously showed that gene-trap knockout of Specc1l in mouse results in early embryonic lethality. We now present a truncation mutant mouse allele, Specc1l ΔC510, that results in perinatal lethality. Specc1l ΔC510/ΔC510 homozygotes showed abnormal palate rugae but did not show cleft palate. However, when crossed with a gene-trap allele, Specc1l cGT/ΔC510 compound heterozygotes showed a palate elevation delay with incompletely penetrant cleft palate. Specc1l cGT/ΔC510 embryos exhibit transient oral epithelial adhesions at E13.5, which may delay shelf elevation. Consistent with oral adhesions, we show periderm layer abnormalities, including ectopic apical expression of adherens junction markers, similar to Irf6 hypomorphic mutants and Arhgap29 heterozygotes. Indeed, SPECC1L expression is drastically reduced in Irf6 mutant palatal shelves. Finally, we wanted to determine if SPECC1L deficiency also contributed to non-syndromic (ns) CL/P. We sequenced 62 Caucasian, 89 Filipino, 90 Ethiopian, 90 Nigerian and 95 Japanese patients with nsCL/P and identified three rare coding variants (p.Ala86Thr, p.Met91Iso and p.Arg546Gln) in six individuals. These variants reside outside of SPECC1L coiled-coil domains and result in milder functional defects than variants associated with syndromic clefting. Together, our data indicate that palate elevation is sensitive to deficiency of SPECC1L dosage and function and that SPECC1L cytoskeletal protein functions downstream of IRF6 in palatogenesis.