Cloning and expression studies on 1-aminocyclopropane-1-carboxylic acid synthase and ethylene receptor genes in Pelargonium

Publikation: Beitrag in Buch/Bericht/Sammelwerk/KonferenzbandAufsatz in KonferenzbandForschungPeer-Review

Autoren

  • T. M. Mutui
  • H. Mibus
  • M. Serek

Externe Organisationen

  • Moi University
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Titel des SammelwerksXXVIII International Horticultural Congress on Science and Horticulture for People (IHC2010)
UntertitelInternational Symposium on Advances in Ornamentals, Landscape and Urban Horticulture
Herausgeber (Verlag)International Society for Horticultural Science
Seiten703-709
Seitenumfang7
ISBN (Print)9789066055254
PublikationsstatusVeröffentlicht - 30 Sept. 2012

Publikationsreihe

NameActa Horticulturae
Band937
ISSN (Print)0567-7572

Abstract

Ethylene biosynthesis is controlled by the enzyme 1-aminocyclopropane-1- carboxylic acid (ACC) synthase. Previous ACC synthase cloning studies revealed a multi-gene family. Degenerate primer pair was used to amplify three DNA fragments using genomic DNA from 'Katinka' leaves. Amplification of several ACC synthase genes with only one PCR reaction was possible due to different number and size of introns in homologue DNA fragments. Sequence analysis of 2 novel partial putative ACC synthase led to their characterization and designation as PzACS3 and PzACS4. The effects of various treatments on ACC synthase and ethylene receptor (ETR) genes during Pelargonium leaf senescence were studied. Gene-specific primers were constructed using already cloned ACC synthase genes in gene bank, synthesized and expression studies were done using semi-quantitative RT-PCR. ACC synthase genes (PzACS3 and PzACS4) transcripts were respectively expressed or undetectable in roots. PhETR1 transcripts were strongly expressed in roots and flower buds whereas PhETR2 was constitutively expressed. Tissue-specific gene expression patterns suggest they have different roles in ethylene biosynthesis and signaling. Transcripts of PzACS3, PzACS4 and PhETR1 genes were expressed in a treatment-specific fashion. Ethylene effect was not apparent on expression of all investigated genes whereas ABA and dark storage respectively increased abundance of pGAC-1 and GACS2 transcripts in 'Katinka'. Conversely, dark storage had no effect on GACS2 transcripts in 'Ganymed'. This was due to either stress-induced ethylene that occurs after dark storage or ABA treatment. Thidiazuron (TDZ) strongly induced expression of the negative acting ethylene receptor, PhETR1. This could have reduced sensitivity of Pelargonium leaves to ethylene with beneficial effect of delaying the onset of leaf senescence.

ASJC Scopus Sachgebiete

  • Agrar- und Biowissenschaften (insg.)
  • Gartenbau

Zitieren

Cloning and expression studies on 1-aminocyclopropane-1-carboxylic acid synthase and ethylene receptor genes in Pelargonium. / Mutui, T. M.; Mibus, H.; Serek, M.
XXVIII International Horticultural Congress on Science and Horticulture for People (IHC2010): International Symposium on Advances in Ornamentals, Landscape and Urban Horticulture. International Society for Horticultural Science, 2012. S. 703-709 (Acta Horticulturae; Band 937).

Publikation: Beitrag in Buch/Bericht/Sammelwerk/KonferenzbandAufsatz in KonferenzbandForschungPeer-Review

Mutui, TM, Mibus, H & Serek, M 2012, Cloning and expression studies on 1-aminocyclopropane-1-carboxylic acid synthase and ethylene receptor genes in Pelargonium. in XXVIII International Horticultural Congress on Science and Horticulture for People (IHC2010): International Symposium on Advances in Ornamentals, Landscape and Urban Horticulture. Acta Horticulturae, Bd. 937, International Society for Horticultural Science, S. 703-709. https://doi.org/10.17660/actahortic.2012.937.85
Mutui, T. M., Mibus, H., & Serek, M. (2012). Cloning and expression studies on 1-aminocyclopropane-1-carboxylic acid synthase and ethylene receptor genes in Pelargonium. In XXVIII International Horticultural Congress on Science and Horticulture for People (IHC2010): International Symposium on Advances in Ornamentals, Landscape and Urban Horticulture (S. 703-709). (Acta Horticulturae; Band 937). International Society for Horticultural Science. https://doi.org/10.17660/actahortic.2012.937.85
Mutui TM, Mibus H, Serek M. Cloning and expression studies on 1-aminocyclopropane-1-carboxylic acid synthase and ethylene receptor genes in Pelargonium. in XXVIII International Horticultural Congress on Science and Horticulture for People (IHC2010): International Symposium on Advances in Ornamentals, Landscape and Urban Horticulture. International Society for Horticultural Science. 2012. S. 703-709. (Acta Horticulturae). doi: 10.17660/actahortic.2012.937.85
Mutui, T. M. ; Mibus, H. ; Serek, M. / Cloning and expression studies on 1-aminocyclopropane-1-carboxylic acid synthase and ethylene receptor genes in Pelargonium. XXVIII International Horticultural Congress on Science and Horticulture for People (IHC2010): International Symposium on Advances in Ornamentals, Landscape and Urban Horticulture. International Society for Horticultural Science, 2012. S. 703-709 (Acta Horticulturae).
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title = "Cloning and expression studies on 1-aminocyclopropane-1-carboxylic acid synthase and ethylene receptor genes in Pelargonium",
abstract = "Ethylene biosynthesis is controlled by the enzyme 1-aminocyclopropane-1- carboxylic acid (ACC) synthase. Previous ACC synthase cloning studies revealed a multi-gene family. Degenerate primer pair was used to amplify three DNA fragments using genomic DNA from 'Katinka' leaves. Amplification of several ACC synthase genes with only one PCR reaction was possible due to different number and size of introns in homologue DNA fragments. Sequence analysis of 2 novel partial putative ACC synthase led to their characterization and designation as PzACS3 and PzACS4. The effects of various treatments on ACC synthase and ethylene receptor (ETR) genes during Pelargonium leaf senescence were studied. Gene-specific primers were constructed using already cloned ACC synthase genes in gene bank, synthesized and expression studies were done using semi-quantitative RT-PCR. ACC synthase genes (PzACS3 and PzACS4) transcripts were respectively expressed or undetectable in roots. PhETR1 transcripts were strongly expressed in roots and flower buds whereas PhETR2 was constitutively expressed. Tissue-specific gene expression patterns suggest they have different roles in ethylene biosynthesis and signaling. Transcripts of PzACS3, PzACS4 and PhETR1 genes were expressed in a treatment-specific fashion. Ethylene effect was not apparent on expression of all investigated genes whereas ABA and dark storage respectively increased abundance of pGAC-1 and GACS2 transcripts in 'Katinka'. Conversely, dark storage had no effect on GACS2 transcripts in 'Ganymed'. This was due to either stress-induced ethylene that occurs after dark storage or ABA treatment. Thidiazuron (TDZ) strongly induced expression of the negative acting ethylene receptor, PhETR1. This could have reduced sensitivity of Pelargonium leaves to ethylene with beneficial effect of delaying the onset of leaf senescence.",
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T1 - Cloning and expression studies on 1-aminocyclopropane-1-carboxylic acid synthase and ethylene receptor genes in Pelargonium

AU - Mutui, T. M.

AU - Mibus, H.

AU - Serek, M.

PY - 2012/9/30

Y1 - 2012/9/30

N2 - Ethylene biosynthesis is controlled by the enzyme 1-aminocyclopropane-1- carboxylic acid (ACC) synthase. Previous ACC synthase cloning studies revealed a multi-gene family. Degenerate primer pair was used to amplify three DNA fragments using genomic DNA from 'Katinka' leaves. Amplification of several ACC synthase genes with only one PCR reaction was possible due to different number and size of introns in homologue DNA fragments. Sequence analysis of 2 novel partial putative ACC synthase led to their characterization and designation as PzACS3 and PzACS4. The effects of various treatments on ACC synthase and ethylene receptor (ETR) genes during Pelargonium leaf senescence were studied. Gene-specific primers were constructed using already cloned ACC synthase genes in gene bank, synthesized and expression studies were done using semi-quantitative RT-PCR. ACC synthase genes (PzACS3 and PzACS4) transcripts were respectively expressed or undetectable in roots. PhETR1 transcripts were strongly expressed in roots and flower buds whereas PhETR2 was constitutively expressed. Tissue-specific gene expression patterns suggest they have different roles in ethylene biosynthesis and signaling. Transcripts of PzACS3, PzACS4 and PhETR1 genes were expressed in a treatment-specific fashion. Ethylene effect was not apparent on expression of all investigated genes whereas ABA and dark storage respectively increased abundance of pGAC-1 and GACS2 transcripts in 'Katinka'. Conversely, dark storage had no effect on GACS2 transcripts in 'Ganymed'. This was due to either stress-induced ethylene that occurs after dark storage or ABA treatment. Thidiazuron (TDZ) strongly induced expression of the negative acting ethylene receptor, PhETR1. This could have reduced sensitivity of Pelargonium leaves to ethylene with beneficial effect of delaying the onset of leaf senescence.

AB - Ethylene biosynthesis is controlled by the enzyme 1-aminocyclopropane-1- carboxylic acid (ACC) synthase. Previous ACC synthase cloning studies revealed a multi-gene family. Degenerate primer pair was used to amplify three DNA fragments using genomic DNA from 'Katinka' leaves. Amplification of several ACC synthase genes with only one PCR reaction was possible due to different number and size of introns in homologue DNA fragments. Sequence analysis of 2 novel partial putative ACC synthase led to their characterization and designation as PzACS3 and PzACS4. The effects of various treatments on ACC synthase and ethylene receptor (ETR) genes during Pelargonium leaf senescence were studied. Gene-specific primers were constructed using already cloned ACC synthase genes in gene bank, synthesized and expression studies were done using semi-quantitative RT-PCR. ACC synthase genes (PzACS3 and PzACS4) transcripts were respectively expressed or undetectable in roots. PhETR1 transcripts were strongly expressed in roots and flower buds whereas PhETR2 was constitutively expressed. Tissue-specific gene expression patterns suggest they have different roles in ethylene biosynthesis and signaling. Transcripts of PzACS3, PzACS4 and PhETR1 genes were expressed in a treatment-specific fashion. Ethylene effect was not apparent on expression of all investigated genes whereas ABA and dark storage respectively increased abundance of pGAC-1 and GACS2 transcripts in 'Katinka'. Conversely, dark storage had no effect on GACS2 transcripts in 'Ganymed'. This was due to either stress-induced ethylene that occurs after dark storage or ABA treatment. Thidiazuron (TDZ) strongly induced expression of the negative acting ethylene receptor, PhETR1. This could have reduced sensitivity of Pelargonium leaves to ethylene with beneficial effect of delaying the onset of leaf senescence.

KW - 1-aminocyclopropane-1-carboxylic acid (ACC) synthase

KW - Ethylene receptor (ETR1) genes

KW - Gene expression

KW - Pelargonium × hortorum

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U2 - 10.17660/actahortic.2012.937.85

DO - 10.17660/actahortic.2012.937.85

M3 - Conference contribution

AN - SCOPUS:84872244422

SN - 9789066055254

T3 - Acta Horticulturae

SP - 703

EP - 709

BT - XXVIII International Horticultural Congress on Science and Horticulture for People (IHC2010)

PB - International Society for Horticultural Science

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