The nodule-specific VfENOD-GRP3 gene encoding a glycine-rich early nodulin is located on chromosome I of Vicia faba L. and is predominantly expressed in the interzone II-III of root nodules

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Helge Küster
  • Gerald Schröder
  • Martin Frühling
  • Uta Pich
  • Mechthild Rieping
  • Ingo Schubert
  • Andreas M. Perlick
  • Alfred Pühler

Externe Organisationen

  • Universität Bielefeld
  • Leibniz-Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK)
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)405-421
Seitenumfang17
FachzeitschriftPlant molecular biology
Jahrgang28
Ausgabenummer3
PublikationsstatusVeröffentlicht - 1 Juni 1995
Extern publiziertJa

Abstract

A nodule-specific cDNA was isolated from a Vicia faba L. nodule cDNA library. Since time course experiments revealed an early expression of this transcript in the nodule, this cDNA coded for an early nodulin and was designated VfENOD-GRP3. Based on tissue print hybridizations, we found a predominant expression of VfENOD-GRP3 transcripts in the interzone II-III region of broad bean root nodules. The encoded early nodulin ENOD-GRP3 was characterized by an N-terminal signal peptide and a C-terminal domain displaying a glycine content of 31%. Sequence analysis of a genomic VfENOD-GRP3 clone revealed that the signal peptide and the glycine-rich domain were specified by two separate exons. Primer extension experiments identified two adjacent transcription start sites for VfENOD-GRP3 transcripts. The common nodulin sequences 'AAAGAT' and 'CTCTT' were present five and three times on both DNA strands of the putative VfENOD-GRP3 promoter, respectively. Additionally, three sequence motifs resembling organ-specific elements of the soybean lbc3 gene promoter and a sequence similar to the binding site 1 for the nodule trans-acting factor Nat2 were identified. From Southern blot data and from sequence analysis of genomic PCR fragments, the presence of a VfENOD-GRP3 gene family was inferred. By PCR experiments using sequence-specific primers and DNA of microisolated chromosomes as a template, this family was located on the long arm of chromosome I.

ASJC Scopus Sachgebiete

Zitieren

The nodule-specific VfENOD-GRP3 gene encoding a glycine-rich early nodulin is located on chromosome I of Vicia faba L. and is predominantly expressed in the interzone II-III of root nodules. / Küster, Helge; Schröder, Gerald; Frühling, Martin et al.
in: Plant molecular biology, Jahrgang 28, Nr. 3, 01.06.1995, S. 405-421.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Download
@article{f04a4271f02344ea83c1255e7027cc69,
title = "The nodule-specific VfENOD-GRP3 gene encoding a glycine-rich early nodulin is located on chromosome I of Vicia faba L. and is predominantly expressed in the interzone II-III of root nodules",
abstract = "A nodule-specific cDNA was isolated from a Vicia faba L. nodule cDNA library. Since time course experiments revealed an early expression of this transcript in the nodule, this cDNA coded for an early nodulin and was designated VfENOD-GRP3. Based on tissue print hybridizations, we found a predominant expression of VfENOD-GRP3 transcripts in the interzone II-III region of broad bean root nodules. The encoded early nodulin ENOD-GRP3 was characterized by an N-terminal signal peptide and a C-terminal domain displaying a glycine content of 31%. Sequence analysis of a genomic VfENOD-GRP3 clone revealed that the signal peptide and the glycine-rich domain were specified by two separate exons. Primer extension experiments identified two adjacent transcription start sites for VfENOD-GRP3 transcripts. The common nodulin sequences 'AAAGAT' and 'CTCTT' were present five and three times on both DNA strands of the putative VfENOD-GRP3 promoter, respectively. Additionally, three sequence motifs resembling organ-specific elements of the soybean lbc3 gene promoter and a sequence similar to the binding site 1 for the nodule trans-acting factor Nat2 were identified. From Southern blot data and from sequence analysis of genomic PCR fragments, the presence of a VfENOD-GRP3 gene family was inferred. By PCR experiments using sequence-specific primers and DNA of microisolated chromosomes as a template, this family was located on the long arm of chromosome I.",
keywords = "glycine-rich early nodulin, interzone II-III predominant expression, physical gene mapping, tissue print hybridization, Vicia faba L.",
author = "Helge K{\"u}ster and Gerald Schr{\"o}der and Martin Fr{\"u}hling and Uta Pich and Mechthild Rieping and Ingo Schubert and Perlick, {Andreas M.} and Alfred P{\"u}hler",
year = "1995",
month = jun,
day = "1",
doi = "10.1007/BF00020390",
language = "English",
volume = "28",
pages = "405--421",
journal = "Plant molecular biology",
issn = "0167-4412",
publisher = "Springer Netherlands",
number = "3",

}

Download

TY - JOUR

T1 - The nodule-specific VfENOD-GRP3 gene encoding a glycine-rich early nodulin is located on chromosome I of Vicia faba L. and is predominantly expressed in the interzone II-III of root nodules

AU - Küster, Helge

AU - Schröder, Gerald

AU - Frühling, Martin

AU - Pich, Uta

AU - Rieping, Mechthild

AU - Schubert, Ingo

AU - Perlick, Andreas M.

AU - Pühler, Alfred

PY - 1995/6/1

Y1 - 1995/6/1

N2 - A nodule-specific cDNA was isolated from a Vicia faba L. nodule cDNA library. Since time course experiments revealed an early expression of this transcript in the nodule, this cDNA coded for an early nodulin and was designated VfENOD-GRP3. Based on tissue print hybridizations, we found a predominant expression of VfENOD-GRP3 transcripts in the interzone II-III region of broad bean root nodules. The encoded early nodulin ENOD-GRP3 was characterized by an N-terminal signal peptide and a C-terminal domain displaying a glycine content of 31%. Sequence analysis of a genomic VfENOD-GRP3 clone revealed that the signal peptide and the glycine-rich domain were specified by two separate exons. Primer extension experiments identified two adjacent transcription start sites for VfENOD-GRP3 transcripts. The common nodulin sequences 'AAAGAT' and 'CTCTT' were present five and three times on both DNA strands of the putative VfENOD-GRP3 promoter, respectively. Additionally, three sequence motifs resembling organ-specific elements of the soybean lbc3 gene promoter and a sequence similar to the binding site 1 for the nodule trans-acting factor Nat2 were identified. From Southern blot data and from sequence analysis of genomic PCR fragments, the presence of a VfENOD-GRP3 gene family was inferred. By PCR experiments using sequence-specific primers and DNA of microisolated chromosomes as a template, this family was located on the long arm of chromosome I.

AB - A nodule-specific cDNA was isolated from a Vicia faba L. nodule cDNA library. Since time course experiments revealed an early expression of this transcript in the nodule, this cDNA coded for an early nodulin and was designated VfENOD-GRP3. Based on tissue print hybridizations, we found a predominant expression of VfENOD-GRP3 transcripts in the interzone II-III region of broad bean root nodules. The encoded early nodulin ENOD-GRP3 was characterized by an N-terminal signal peptide and a C-terminal domain displaying a glycine content of 31%. Sequence analysis of a genomic VfENOD-GRP3 clone revealed that the signal peptide and the glycine-rich domain were specified by two separate exons. Primer extension experiments identified two adjacent transcription start sites for VfENOD-GRP3 transcripts. The common nodulin sequences 'AAAGAT' and 'CTCTT' were present five and three times on both DNA strands of the putative VfENOD-GRP3 promoter, respectively. Additionally, three sequence motifs resembling organ-specific elements of the soybean lbc3 gene promoter and a sequence similar to the binding site 1 for the nodule trans-acting factor Nat2 were identified. From Southern blot data and from sequence analysis of genomic PCR fragments, the presence of a VfENOD-GRP3 gene family was inferred. By PCR experiments using sequence-specific primers and DNA of microisolated chromosomes as a template, this family was located on the long arm of chromosome I.

KW - glycine-rich early nodulin

KW - interzone II-III predominant expression

KW - physical gene mapping

KW - tissue print hybridization

KW - Vicia faba L.

UR - http://www.scopus.com/inward/record.url?scp=0029310582&partnerID=8YFLogxK

U2 - 10.1007/BF00020390

DO - 10.1007/BF00020390

M3 - Article

C2 - 7632912

AN - SCOPUS:0029310582

VL - 28

SP - 405

EP - 421

JO - Plant molecular biology

JF - Plant molecular biology

SN - 0167-4412

IS - 3

ER -

Von denselben Autoren