Characterization of the soybean early nodulin cDNA clone GmENOD55.

C. de Blank; P. Mylona; P. Katinakis; T. Bisseling; H. Franssen; W.C. Yang

doi:10.1007/BF00028987

Characterization of the soybean early nodulin cDNA clone GmENOD55.

C. de Blank, P. Mylona, P. Katinakis, T. Bisseling, H. Franssen, W.C. Yang

Laboratory of Molecular Biology

Research output: Contribution to journal › Article › Academic › peer-review

26 Citations (Scopus)

Abstract

Two cDNA clones of the soybean early nodulin GmENOD55 were characterized. These clones may represent two members of the soybean early nodulin gene family GmENOD55. GmENOD55 has an N-terminal signal peptide and it contains an internal domain consisting of proline and serine residues. Analyses of nodules lacking infection threads and intracellular bacteria suggest that the GmENOD55 gene is first expressed after release ofBradyrhizobium japonicum in plant cells. This conclusion is supported byin situ hybridization studies showing that the expression is restricted to the infected cell type.

Original language	English
Pages (from-to)	1167-1171
Journal	Plant Molecular Biology
Volume	22
DOIs	https://doi.org/10.1007/BF00028987
Publication status	Published - 1993

Keywords

Bradyrhizobium
early nodulin
soybean

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10.1007/BF00028987

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@article{3a62a0a961014832b0be82d6a45cd6c7,

title = "Characterization of the soybean early nodulin cDNA clone GmENOD55.",

abstract = "Two cDNA clones of the soybean early nodulin GmENOD55 were characterized. These clones may represent two members of the soybean early nodulin gene family GmENOD55. GmENOD55 has an N-terminal signal peptide and it contains an internal domain consisting of proline and serine residues. Analyses of nodules lacking infection threads and intracellular bacteria suggest that the GmENOD55 gene is first expressed after release ofBradyrhizobium japonicum in plant cells. This conclusion is supported byin situ hybridization studies showing that the expression is restricted to the infected cell type.",

keywords = "Bradyrhizobium, early nodulin, soybean",

author = "{de Blank}, C. and P. Mylona and P. Katinakis and T. Bisseling and H. Franssen and W.C. Yang",

year = "1993",

doi = "10.1007/BF00028987",

language = "English",

volume = "22",

pages = "1167--1171",

journal = "Plant Molecular Biology",

issn = "0167-4412",

publisher = "Springer",

}

TY - JOUR

T1 - Characterization of the soybean early nodulin cDNA clone GmENOD55.

AU - de Blank, C.

AU - Mylona, P.

AU - Katinakis, P.

AU - Bisseling, T.

AU - Franssen, H.

AU - Yang, W.C.

PY - 1993

Y1 - 1993

N2 - Two cDNA clones of the soybean early nodulin GmENOD55 were characterized. These clones may represent two members of the soybean early nodulin gene family GmENOD55. GmENOD55 has an N-terminal signal peptide and it contains an internal domain consisting of proline and serine residues. Analyses of nodules lacking infection threads and intracellular bacteria suggest that the GmENOD55 gene is first expressed after release ofBradyrhizobium japonicum in plant cells. This conclusion is supported byin situ hybridization studies showing that the expression is restricted to the infected cell type.

AB - Two cDNA clones of the soybean early nodulin GmENOD55 were characterized. These clones may represent two members of the soybean early nodulin gene family GmENOD55. GmENOD55 has an N-terminal signal peptide and it contains an internal domain consisting of proline and serine residues. Analyses of nodules lacking infection threads and intracellular bacteria suggest that the GmENOD55 gene is first expressed after release ofBradyrhizobium japonicum in plant cells. This conclusion is supported byin situ hybridization studies showing that the expression is restricted to the infected cell type.

KW - Bradyrhizobium

KW - early nodulin

KW - soybean

U2 - 10.1007/BF00028987

DO - 10.1007/BF00028987

M3 - Article

SN - 0167-4412

VL - 22

SP - 1167

EP - 1171

JO - Plant Molecular Biology

JF - Plant Molecular Biology

ER -

Characterization of the soybean early nodulin cDNA clone GmENOD55.

Abstract

Keywords

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