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100 Years of phenogenetics: Valentin Haecker and his examination of the phenotype

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Abstract

Following the ‘rediscovery’ of Mendel’s work around 1900 the study of genetics grew rapidly and multiple new inheritance theories quickly emerged such as Hugo de Vries’ “Mutation Theory” (1901) and the “Boveri–Sutton Chromosome Theory” (1902). Mendel’s work also caught the attention of the German geneticist Valentin Haecker, yet he was generally dissatisfied the simplicity of Mendelian genetics as he believed that inheritance and the expression of various characteristics appeared to be much more complex than the proposed “on–off hypotheses”. Haecker’s primary objection was that Mendelian-based theories still failed to bridge the gap between hereditary units and phenotypic traits. Haecker thus set out to bridge this gap in his research program, which he called Phänogenetik (“phenogenetics”). He outlined his work in a special study “Entwicklungsgeschichtliche Eigenschaftsanalyse (Phänogenetik)” in 1918. 2018 thus marks the 100th anniversary of Haecker’s seminal publication, which was devoted to the analysis of the phenotype and highlighted the true complexity of heredity. This article takes a specific look at Haecker and his work, while also illustrating how this often forgotten scientist influenced the field of genetics and other scientists.

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Notes

  1. Haecker did spend some time discussing Mendelian genetics in later publications such as the two chapters he devoted to Mendelian rules in his 1921 book “Allgemeine Vererbungslehre” (General Genetics).

  2. https://medium.com/@johnhawks/the-man-who-tried-to-catalog-humanity-b433c3f31872. Accessed 26 October 2018.

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Correspondence to Elizabeth Watts.

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Uwe Hoßfeld, declares that he has no conflict of interest. Georgy S. Levit, declares that he has no conflict of interest. Elizabeth Watts, declares that she has no conflict of interest.

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Communicated by S. Hohmann.

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Hoßfeld, U., Levit, G.S. & Watts, E. 100 Years of phenogenetics: Valentin Haecker and his examination of the phenotype. Mol Genet Genomics 294, 445–456 (2019). https://doi.org/10.1007/s00438-018-1519-1

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