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Immunocytochemistry of pectins in shoot apical meristems: consequences for intercellular adhesion

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Summary.

The nature of pectins (acidic, methyl-, or acetyl-esterified) in the shoot meristem of Sinapis alba was assessed by immunocytochemistry with the 2F4 monoclonal antibody in light and electron microscopy. This antibody is specific for “egg-boxes” – the polygalacturonic acid conformation induced by calcium as described in Liners et al. (Plant Physiol. 99: 1099–1104, 1992). Hardly any acidic pectin was detected in meristem walls; the pectins were largely methyl-esterified and esterified by acetyl groups and/or other esters. After in situ chemical or enzymatic de-esterification, labeling was distributed over the primary wall and the middle lamella of meristematic cells. Acidic pectin and Ca2+-cross-linked homogalacturonans were absent from the pit fields, where plasmodesmata traverse the middle lamella. The type and distribution of pectins are discussed in relation to cellular adhesion between active meristem cells.

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Abbreviations

HG:

homogalacturonan

PME:

pectin methylesterase

RG I:

rhamnogalacturonan I

RG II:

rhamnogalacturonan II

XGA:

xylogalacturonan

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Correspondence to P. Van Cutsem.

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Correspondence and reprints: Unité de Recherches en Biologie Cellulaire Végétale, Département de Biologie, Facultés Universitaires Notre-Dame de la Paix, rue de Bruxelles 61, 5000 Namur, Belgium.

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Sobry, S., Havelange, A. & Van Cutsem, P. Immunocytochemistry of pectins in shoot apical meristems: consequences for intercellular adhesion. Protoplasma 225, 15–22 (2005). https://doi.org/10.1007/s00709-005-0089-3

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  • DOI: https://doi.org/10.1007/s00709-005-0089-3

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