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Comparison of the MpEF1alpha and CaMV35 promoters for application in Marchantia polymorpha overexpression studies.

Althoff F, Kopischke S, Zobell O, Ide K, Ishizaki K, Kohchi T, Zachgo S. · 2014 · Transgenic Res   research

doi:10.1007/s11248-013-9746-z   PMID:24036909

Linked genes (2)  1 core 1 peripheral

Gene ID Name Evidence / Role Function (this paper)
Mp3g23400 MpEF1 experimental subject Endogenous elongation factor 1-alpha promoter characterized as a constitutive driver for Marchantia overexpression/silencing; the proMpEF1α::GUS reporter showed strong meristematic and broadly ubiquitous expression, outperforming CaMV35S. Whole-mount in situ hybridization of endogenous MpEF1α mRNA matched the GUS pattern (meristematic zones of gemmae; egg cells, neck and venter cells of young archegonia).
Mp4g13430
MpH4 paper
MpH4c nomenclature
experimental tool Marchantia Histone H4 homologue (MpHistone4 / MpH4), isolated here as a cell-division marker; used as an antisense in-situ probe to validate the whole-mount in situ hybridization method. Its signal marked dividing cells around the meristematic zones and gemma margins. Used as a tool/marker, not the subject of study.