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Analysis of randomly mutated AlSRKb genes reveals that most loss-of-function mutations cause defects in plasma membrane localization.

The New phytologist - 1 Nov 2024

Yamamoto Masaya, Ohtake Shotaro, Shinozawa Akihisa, Shirota Matsuyuki, Mitsui Yuki, Kitashiba Hiroyasu

Abstract excerpt

Only very limited information is available on why some nonsynonymous variants severely alter gene function while others have no effect. To identify the characteristic features of mutations that strongly influence gene function, this study focused on SRK which encodes a highly polymorphic receptor kinase expressed in stigma papillary cells that underlies a female determinant of self-incompatibility in...

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Identifiers

PMID: 39279039
DOI: 10.1111/nph.20111

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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