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BAG. Journal of basic and applied genetics

versión On-line ISSN 1852-6233

BAG, J. basic appl. genet. vol.30 no.1 Ciudad Autónoma de Buenos Aires jun. 2019

 

SHORT COMMUNICATION

Partial sequences of the gene that codifies for the transcription factor VPHSFB1 in Vasconcellea pubescens. First report

Secuencias parciales del gen que codifica para el factor de transcripción VPHSFB1 en Vasconcellea pubescens. Primer reporte

 

Arizala-Quinto E. D1, Viteri G.1 Idrovo-Espín F.M.1,2

1 Universidad de Las Américas UDLA. Facultad de Ingeniería y Ciencias Aplicadas. Calle José Queri s/n entre Av. Eloy Alfaro y Granados
2 Universidad Central del Ecuador. Facultad de Ciencias Químicas. Francisco Viteri s/n y Gato Sobral. Quito-Ecuador

Corresponding author: F.M Idrovo-Espín f.idrovo@udlanet.ec

DOI: 10.35407/bag.2019.XXX.01.01

Received: 12/12/2017
Accepted: 10/08/2018


ABSTRACT

Plant heat stress transcription factors (HSFs) are involved in the response to heat. In Arabidopsis thaliana the HSFs genes are completely identified, however there was no information available about these genes in Vasconcellea pubescens (Chamburo) until now. In this preliminary work we describe the VPHSFB1 gene of V. pubescens (gene expression evaluated by RT-PCR and the partial sequence) that was induced by the increment of temperature. From our results, VPHSFB1 could be used as a heat response marker gene in tropical species.

Key words: Caricaceae; Gene expression; Heat.

RESUMEN

Los factores de transcripción del estrés por calor en plantas (HSFs) están involucrados en la respuesta al calor. En Arabidopsis thaliana los genes HSFs están completamente identificados, sin embargo no había información disponible sobre estos genes en Vasconcellea pubescens (Chamburo) hasta ahora. En este trabajo preliminar describimos el gen VPHSFB1 de V. pubescens (expresión génica evaluada por RT-PCR y la secuencia parcial) que fue inducido por el incremento de temperatura. A partir de nuestros resultados, se podría usar a VPHSFB1 como un gen marcador de respuesta a calor en especies tropicales.

Palabras clave: Caricaceae; Expresión génica; Calor.


 

INTRODUCTION

Plant heat stress transcription factors (HSFs) are essential components of the signal transduction involved in the expression of genes responsive to this kind of abiotic stress (Nover et al., 2001). In A. thaliana 21 members of HSFs belonging to three genes classes A, B and C, have been identified (Kotak et al., 2004). Among these, ATHSFB1 (Class B) is necessary for the expression of heat stress inducible genes (as heat shock protein genes) that are involved in thermotolerance (Ikeda et al., 2011). Caricaceae is a family composed by six genera, two of them are Vasconcellea and Carica. The 21 species that belong to genus Vasconcellea (collectively known as highland papayas) are distributed in South America, endemically in some countries, as Ecuador (Scheldeman et al., 2011). It has been estimated that Vasconcellea diverged from Carica 25 Ma ago (Carvahlo and Renner, 2012).
More specifically the exotic species V. pubescens has interesting properties and uses, ranging from high levels of antioxidants (Simirgiotis et al., 2009), gastric ulcers treatments (Mello et al., 2008), dermal antitumoral therapy (Dittz et al., 2015) to biofilm production based on Papain against cavities (Torres and Obando, 2016). In this preliminary work, we report the partial sequence of the V. pubescens VPHSFB1 gene, a phylogenetic analysis with related sequences and the expression banding pattern of VPHSFB1 after temperature increase.

MATERIALS AND METHODS

Oligonucleotides for RT-PCR amplification and further sequencing of the amplicons were designed from the CPHSFB1 gene reported by Tarora et al. (2010). Germinated seedlings (75 days old) were subjected to increment of temperature (from 25° C to 33° C or 45° C) for a period of 4 hs; seedlings at 25° C were used as controls. After applying the temperature treatment, RNA was extracted from leaves (PureLink RNA MiniKit, Ambion), then RTPCR was performed (Superscript III One Step RT-PCR, Invitrogen) and, finally, agarose gel electrophoresis (1% agarose, 45 min, 80 volts) was performed and documented. Amplicons were sequenced twice in UDLA research laboratory (ABI 3130 Genetic Analyzer). Phylogenetic analysis was made in comparison with HSFs selected sequences with MEGA7 (Kumar et al., 2016).

RESULTS AND DISCUSSION

Phylogenetic analysis of partial sequences of the VPHSFB1gene
From a PCR product (plants at 25° C) we obtained two partial sequences of V. pubescens heat stress transcription factor (Figure 1), hereinafter referred to as VPHSB1a (340 bp) and VPHSB1b (330 bp).


Figure 1.
Clustal w alignment of partial sequences of the VPHSFB1 gene.

Despite the fact that the sequences were only fragments of the VPHSFB1 gene, the phylogenetic tree (Figure 2) exhibited one major clade comprising the HSF sequences of V. pubescens, A. thaliana, C. papaya and Brassica rapa. Within this clade, a subclade was formed with the Caricaceae members; this was the expected topology since V. pubescens and papaya are more related between them than with Arabidopsis. The other sequences in this analysis remained unsolved. Interestingly, the sequences in the Caricaceae subclade seemed to have accumulated changes earlier that the ancestral lineage split between Arabidopsis and Brassica. This may have been because V. pubescens and papaya are strictly tropical species, as Carvahlo and Renner (2012) have shown in their biogeographic study. Therefore, it is feasible that Caricaceae developed specialized HSF genes in order to cope with higher temperatures earlier than Arabidopsis or Brassica, which are less adapted to tropical climates. From the alignment of all sequences (not shown), the highest identity percentages were obtained by comparing VPHSFB1 with CPHSFB1, thus, we conclude that these sequences are orthologs among them.


Figure 2.
Maximum Likelihood phylogenetic tree based on a MUSCLE alignment of partial selected sequences HSFs genes (C. papaya CPHSFB1/AB506766.1, A. thaliana ATHSFB1/ AT4G36990, Brassica rapa BRHSF/EU186351.1, Populus trichocarpa PTHSF31/GI566202080, Vitis vinifera VVHSF30/NM001303086.1). The tree was rooted with 20SPAB1 (AT1G16470.1) that encodes for the 20S proteasome subunit PAB1 in A. thaliana (Iida et al., 2009). The identity percentage of orthologs from V. pubescens, A. thaliana and C. papaya are shown below.

Expression banding pattern of the VPHSFB1 gene
Although the expression of VPHSFB1 is constitutive at the assayed temperatures, the intensity of bands obtained by gel electrophoresis (Figure 3) increased at higher temperatures. Previously Tarora et al. (2010) characterized the ortholog CPHSFB1 gene in papaya. In a Northern blot analysis, it was observed that this gene accumulated transcripts differentially after temperature increase (from 24° C to 42° C) and, thus it is responsive to heat stress. This behavior is similar to the observed in our analysis, which revealed the involvement of VPHSFB1 in the response to temperature increment and, probably, in heat stress. We conclude that an ortholog VPHSFB1 gene is present in the genome of V. pubescens, which is responsive to temperature increment, and that this gene could be used as a marker for heat stress assays in this tropical species.


Figure 3.
Banding pattern obtained from control plants (25° C) and plants under temperature increase (33.5° C and 45° C). 18S gene expression was used as a positive control. Controls with no template showed any band. The assay was made in triplicates with similar results.

ACKNOWLEDGEMENTS

To the Ministry of the Environment of Ecuador (MAE) for the permissions granted (MAEDNB- CM-2017-0063), to Lien González for her support and valuable comments. This work was supported by UDLA (grant INV/F/PPI/1/0814).

REFERENCES

1. Carvalho F.A., Renner S.S. (2012) A dated phylogeny of the papaya family (Caricaceae) reveals the crop’s closest relatives and the family’s biogeographic history. Mol. Phylogenet. Evol. 65: 46-53.

2. Dittz D., Figueiredo C., Lemos F., Viana C., Andrade S., Souza-Fagundes E., Fujiwara R.T., Salas C.E., Lopes M. (2015) Antiangiogenesis, Loss of Cell Adhesion and Apoptosis Are Involved in the Antitumoral Activity of Proteases from V. cundinamarcensis (C. candamarcensis) in Murine Melanoma B16F1. Int. J. Mol. Sci. 16: 7027-7044.         [ Links ]

3. Iida K., Fukami-Kobayashi K., Toyoda A., Sakaki Y., Kobayashi M., Seki M., Shinozaki K. (2009) Analysis of multiple occurrences of alternative splicing events in Arabidopsis thaliana using novel sequenced full-length cDNAs. DNA Res. 16: 155-164.         [ Links ]

4. Ikeda M., Mitsuda N., Ohme-Takagi M. (2011). Arabidopsis HsfB1 and HsfB2b act as repressors of the expression of heatinducible Hsfs but positively regulate the acquired thermotolerance. Plant Physiol. 157(3): 1243-1254.         [ Links ]

5. Kotak S., Port M., Ganguli A., Bicker F., von Koskull-Doring P. (2004) Characterization of C-terminal domains of Arabidopsis heat stress transcription factors (Hsfs) and identification of a new signature combination of plant class A Hsfs with AHA and NES motifs essential for activator function and intracellular localization. Plant J. 39: 98-112.         [ Links ]

6. Kumar S., Stecher G., Tamura K. (2016) MEGA7: Molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol. Biol. Evol. 33: 1870-1974.         [ Links ]

7. Mello V., Gomes M., Lemos F., Delfino J., Andrade S., Lopes M., Salas C. (2008) The gastric ulcer protective and healing role of cysteine proteinases from Carica candamarcensis. Phytomedicine 15: 237-244.         [ Links ]

8. Nover L., Bharti K., Döring P., Kumar M.S., Ganguli A., Scharf K.D. (2001) Arabidopsis and the heat stress transcription factor world: how many heat stress transcription factors do we need? Cell Stress Chaperon 6: 177-189.         [ Links ]

9. Scheldeman X., Kyndt T., Coppens d’Eeckenbrugge G., Ming R., Drew R., Droogenbroeck B., Van Damme P., Moore P. (2011). Vasconcellea. In: Kole C. (Ed.) Wild Crop Relatives: Genomic and Breeding Resources. Springer-Verlag, Berlin, pp. 213-249.

10. Simirgiotis M., Caligari P., Schmeda- Hirschmann G. (2009) Identification of phenolic compounds from the fruits of the mountain papaya Vasconcellea pubescens A. DC. grown in Chile by liquid chromatography-UV detection-mass spectrometry. Food Chem. 115: 775-784.         [ Links ]

11. Tarora K., Tamaki M., Shudo A., Urasaki N., Matsumura H., Adaniya S. (2010) Cloning of a heat stress transcription factor, CphsfB1, that is constitutively expressed in radicles and is heat-inducible in the leaves of Carica papaya. Plant Cell Tissue Organ Cult. 102: 69-77.         [ Links ]

12. Torres K., Obando G. (2016) Rapid enzimatic disruption of Enterococcus faecalis biofilm using Carica pubescens: a pilot study. WMCCR 2: 1-4.         [ Links ]

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