Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)

H. G. Brunner*, H. T. Bruggenwirth, W. Nillesen, G. Jansen, B. C.J. Hamel, R. L.E. Hoppe, C. E.M. De Die, C. J. Howeler, B. A. Van Oost, B. Wieringa, H. H. Ropers, H. J.M. Smeets

*Corresponding author for this work

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Abstract

In patients with myotonic dystrophy (DM), the severity of clinical signs is correlated with the length of a (CTG)(n) trinucleotide repeat sequence. This sequence tends to expand in subsequent generations. In order to examine the kinetics of this process and, in particular, the influence of the mutant- allele size and the sex of the transmitting parent, we have studied (CTG)(n) repeat lengths in the offspring of 38 healthy carriers with small mutations (less than 100 CTG trinucleotides, mean length [CTG]67). In these studies, we found a weakly positive correlation between the size of the mutation in the carrier parents and that in their offspring. Furthermore, we observed that, in the offspring of male transmitters, repeat lengths exceeding 100 CTG trinucleotides were much more frequent than in the offspring of carrier females (48 [92%] of 52 vs. 7 [44%] of 16, P = .0002). Similarly, in genealogical studies performed in 38 Dutch DM kindreds, an excess of nonmanifesting male transmitters was noted, which was most conspicuous in the generation immediately preceding that with phenotypic expression of DM. Thus, two separate lines of evidence suggest that the sex of the transmitting parent is an important factor that determines DM allele size in the offspring. On the basis of our data, we estimate that when both parents are asymptomatic, the odds are approximately 2:1 that the father carries the DM mutation. Because expansion of the CTG repeat is more rapid with male transmission, negative selection during spermatogenesis may be required to explain the exclusive maternal inheritance of severe congenital onset DM.

Original languageEnglish
Pages (from-to)1016-1023
Number of pages8
JournalAmerican Journal of Human Genetics
Volume53
Issue number5
Publication statusPublished - 1993
Externally publishedYes

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