ZRS mutations in two Chinese Han families featuring triphalangeal thumbs and preaxial polydactyly.
- Author:
Ximeng ZHAO
1
,
2
,
3
;
Wei YANG
;
Miao SUN
;
Xue ZHANG
Author Information
- Publication Type:Journal Article
- MeSH: Asian Continental Ancestry Group; genetics; Female; Hand Deformities, Congenital; genetics; Haplotypes; Humans; Male; Mutation; Polydactyly; genetics; Regulatory Sequences, Nucleic Acid; Thumb; abnormalities
- From: Chinese Journal of Medical Genetics 2016;33(3):281-285
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo identify the causative mutations in two Chinese Han families featuring triphalangeal thumbs (TPT) and preaxial polydactyly (PPD).
METHODSBlood samples were collected from 9 members (2 affected) from family 1 and 14 members (7 affected) from family 2. After genomic DNA was extracted, the ZPA regulatory sequence (ZRS) region was analyzed with real-time quantitative PCR (qPCR) and Sanger sequencing. For family 1, haplotypes compassing the ZRS were also analyzed with short tandem repeats (STR) and single nucleotide changes.
RESULTSNo copy number mutation around the ZRS region was found in both families. Two heterogeneous mutations in the ZRS (406A>G and 105C>G) were found to co-segregate with the TPT/PPD malformation in family 1 and 2, respectively. Neither mutation was detected in 200 healthy individuals. Haplotype analysis and Sanger sequencing of family 1 indicated that the first TPT/PPD patient in the family was both germline and somatic mosaic for the 406A>G mutation.
CONCLUSIONTwo pathogenic ZRS mutations, 105C>G and 406A>G, have been identified in two Chinese Han families with TPT/PPD, among which the 406A>G mutation was de novo.
