Somatic reversion in Wiskott‐Aldrich syndrome: Case reports and mechanistic insights

• Published in: Scandinavian journal of immunology Vol. 100; no. 5; pp. e13408 - n/a
• Main Authors: Rikhi, Rashmi, Basu, Suprit, Arora, Kanika, Chan, Koon‐Wing, Jindal, Ankur Kumar, Rawat, Amit, Lau, Yu‐lung, Suri, Deepti
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.11.2024
• Subjects: Amino acid sequence; Case reports; CD3 antigen; DNA sequencing; Frameshift Mutation; Gene deletion; Genomic analysis; Humans; Leukocytes (mononuclear); Lymphocytes; Lymphocytes B; Lymphocytes T; Male; Mouth Mucosa; mRNA; Mucosa; Mutation; Nucleotide sequence; Peripheral blood mononuclear cells; Reversion; T-Lymphocytes - immunology; Wiskott-Aldrich syndrome; Wiskott-Aldrich Syndrome - genetics; Wiskott-Aldrich Syndrome - immunology; Wiskott-Aldrich Syndrome Protein - genetics
• ISSN: 0300-9475; 1365-3083; 1365-3083
• DOI: 10.1111/sji.13408

This report describes two brothers from India and a Chinese patient with somatic reversion of an inherited deleterious mutation in the WAS gene. Both the Indian siblings had inherited a single nucleotide deletion causing a frameshift mutation (c.1190del, p.Pro397Argfs*48) (variant 1: marked in blue) from the mother. Another variant (variant 2: marked in red), a 12‐nucleotide deletion at position 1188–1199 (c.1188_1199del, p.P401_P404del) was also found, which resulted in restoration of the frame and subsequent rescue of the protein sequence. DNA sequencing from buccal mucosal cells revealed only the inherited variant (variant 1), while no reversion mutation was identified in the mucosal cells. Similarly, the Chinese patient was found to have a novel germline 14‐base duplication (ACGAAAATGCTTGG) c.120_132 + 1dup (variant 1). This resulted in abolishment of the original splice junction coupled with the creation of a new junction 14 bases 3′ and a frameshift mutation with predicted protein truncation p. Thr45Aspfs*. DNA from the patient's PBMC showed co‐existence of wild‐type and mutated sequences, but only the mutant was present in the buccal cells. Genomic and mRNA analysis of the isolated CD3+ T lymphocytes, CD3‐ mononuclear cells, and EBV‐transformed B lymphocytes indicated that the reverant variant (germline variant was restored to wild‐type sequence) were selectively found in CD3+ T lymphocytes.