Germline mosaicism for an alanine to valine substitution at residue beta 140 in hemoglobin Puttelange, a new variant with high oxygen affinity.

Abstract

Hb Puttelange [beta 140(H18)Ala-->Val] was found as a de novo mutation in two siblings of a French family suffering from polycythemia. Both parents were phenotypically normal and exclusion of paternity has been ruled out by the study of several polymorphic markers located on different chromosomes. The structural modification of Hb Puttelange was established by reversed-phase HPLC analysis of the tryptic digest of the abnormal chain. The amino acid composition of an abnormal beta T14 peptide revealed that one of the four residues of Ala was replaced by a Val. Tandem mass spectrometry demonstrated that the substitution concerned position beta 140 (H18). This hemoglobin displays an increased oxygen affinity that is responsible for the polycythemia. De novo mutations, as demonstrated again in the case of this variant, have the highest probabilities of detection when they lead to pathological manifestations. They may result either from a somatic mutation in a very early stage of the embryological development of the propositus or may have a parental origin with occurrence of a germline mosaicism. The study of the beta-globin gene indicated that this case of Hb Puttelange probably arose from a mutation affecting a part of the germline of the father, therefore leading to a true recurrence risk.

• Authors: H Wajcman, E Girodon, D Promé, M L North, F Plassa, I Duwig, J Kister, J P Bergerat, F Oberling, E Lampert
• Journal: Human genetics (Hum Genet) Vol. 96 Issue 6 Pg. 711-6 (Dec 1995) ISSN: 0340-6717 [Print] Germany
• PMID: 8522332 (Publication Type: Case Reports, Journal Article)

Chemical References

• Genetic Markers
• Hemoglobins, Abnormal
• Macromolecular Substances
• Oxyhemoglobins
• Peptide Fragments
• hemoglobin Puttelange
• Globins
• Valine
• Alanine

Topics

• Adult
• Aged
• Alanine
• Amino Acid Sequence
• Fathers
• Female
• Genetic Markers
• Genetic Variation
• Genomic Imprinting
• Globins (genetics)
• Hemoglobins, Abnormal (chemistry, genetics, metabolism)
• Humans
• Macromolecular Substances
• Male
• Middle Aged
• Molecular Sequence Data
• Mosaicism
• Oxyhemoglobins (metabolism)
• Pedigree
• Peptide Fragments (chemistry, isolation & purification)
• Point Mutation
• Polycythemia (blood, genetics)
• Polymorphism, Genetic
• Valine