A yeast-based model system for cloning secreted and membrane proteins

A yeast-based model system for cloning secreted and membrane proteins

MARCELO J. SURPILI¹, BERND MÜLLER-RÖBER² and LOTHAR WILLMITZER²

¹Institut für Genbiologische Forschung Berlin GmbH, Ihnestra"se 63, 14195 Berlin, Germany

²Max-Planck-Institut für molekulare Pflanzenphysiologie (MPI-MOPP), Karl-Liebknecht-Stra"se 25 Haus 20, 14476 Golm, Germany

Manuscript received on March 15, 2002; accepted for publication on July 31, 2002;

presented by LEWIS J. GREENE

ABSTRACT

The targeting of proteins to cell organelles and membranes, or of proteins destined to secretion, is coordinated by signal sequences located at the 5´-end of their respective genes. A signal sequence trap system was envisaged in which a truncated version of the yeast acid phosphatase pho5 gene lacking the start codon and signal sequence could serve as a reporter gene. A fraction enriched in 5´-end fragments obtained by PCR from a potato guard-cell cDNA library was cloned in frame to the acid phosphatase gene and the acid phosphatase activity was assayed directly in yeast colonies grown on selective medium. Putative signal sequences targeting the acid phosphatase to the membrane or to the outside of the cell were used to screen the cDNA bank in order to recover the original full-size sequence which gave rise to the signal sequence. Two unknown sequences displaying marked tissue-specific expression were retrieved, one of them (YE139) with a higher expression level in green buds and stem cells, and the other one (YE290) with a higher expression level in androceum, gyneceum, and roots. The limitations of the system are further analyzed using other sequences as control.

Key words: signal sequences, potassium channel, yeast acid phosphatase, library screening.

1. INTRODUCTION

The partitioning of biochemical processes in organelles of eukaryotic cells is one of the major accomplishments of nature. Major targets for the partitioning of proteins in eukaryotes include mitochondria, chloroplasts, peroxisomes, glyoxysomes, and the nucleus. Proteins destined to these organelles are translated on free polyribosomes in the cytosol and, concomitantly or shortly thereafter, they are imported into the appropriate organelle based on the recognition of specific targeting signals. In contrast, the transport of proteins to the cell membrane for insertion or secretion occurs by a default secretory pathway, in which the targeted protein moves from the endoplasmic reticulum (ER) to the Golgi apparatus, and then to transport vesicles (Hadlington and Denecke 2000). Whether a protein remains bound to the membrane or is secreted depends on its signal sequence.

Studies on the biosynthesis of secretory proteins in prokaryotes and eukaryotes have shown that most of these proteins are synthesized as precursors containing an additional of 15-30 amino acids at the N-terminal end of the molecule (Milstein et al. 1982). These transient N-terminal extensions, known as signal peptides (Blobel and Dobberstein 1975), are responsible for most of the protein sorting that occurs in the cell. Many membrane proteins on the inner and outer surface of the cell membrane have an important role in responding to changes in the external environment (Smith 1990). In plants, the greatest changes in the plasma membrane protein profile occur during the early stages of development, including floral induction and, to a lesser extent, in later stages such as seed formation and senescence. These temporal and spatial changes have been studied in detail in highly purified tobacco leaf plasma membrane fractions (Masson and Rossignol 1995).

The aim of the present study was to establish a system for screening cDNA libraries to trap signal sequences from proteins trafficking along the secretory pathway. The approach consisted of substituting the signal sequence of a known secretory protein for unknown sequences obtained preferentially from the 5´-ends of the library cDNA clones, where signal sequences are usually found. The signal sequences would then be recovered and used as probes to screen the cDNA bank for the full-size clone. The secretory protein chosen as a reporter in this case was the acid phosphatase PHO5 (E. C. 3.1.3.2) from Saccharomyces cerevisiae, the main enzyme in a family of four acid phosphatases in this yeast (Oshima 1997). Gene fusions to pho5 provide a convenient system for analyzing gene regulation, and for studying the signals involved in the proper localization of proteins in yeast (Sidhu and Bollon 1987, Lopandic et al. 1987). Arima et al. (1983) identified a 17-amino acid signal peptide in the repressible pho5 gene. In the present study, yeast PHO5 mutants were used, and shuttle vectors containing a truncated version of the pho5 gene, i.e., the nucleotide sequence corresponding to the protein without its native signal sequence, were constructed. The constructs containing unknown sequences in front of the truncated pho5 gene were then used for the transformation and partial complementation of mutant cells on adequate medium. PHO5 activity was detected by direct staining of yeast colonies grown on a plate using diazo-coupling dyes. The red diazocompound complex formed during the reaction cannot enter the cytoplasm, so the reaction must occur outside the cell. The presence of acid phosphatase outside the cell would thus indicate that a signal sequence was responsible for its secretion.

2. MATERIALS AND METHODS

ENZYMES AND CHEMICALS

DNA restriction and modification enzymes were purchased from Boehringer (Mannheim, Germany) and New England Biolabs (Beverly, MA). Chemicals were from Sigma (Deisenhofen, Germany), Boehringer (Mannheim, Germany) or Merck (Darmstadt, Germany). Primers T3 (5´-AATTAACCCTCACTAAAGGG) and T7 (5´-GTAATACGACTCACTATAGGGC) were purchased from LKB Pharmacia. All other primers for sequencing or PCR reactions were purchased from TibMolBiol, Berlin, Germany.

PLANTS, BACTERIAL AND YEAST STRAINS AND GROWTH CONDITIONS

Solanum tuberosum L. cv. Désirée was obtained from Saatzucht Fritz Lange GmbH (Bad Schwartau, Germany). The plants were grown in a greenhouse in individual pots and were watered daily with ~ 16h light (22°C) and 8h dark (15°C) cycles.

Escherichia coli was cultured at 37°C in Luria-Bertani medium using standard methods (Sambrook et al. 1989). E. coli strains DH5a (Bethesda Research Laboratories, Gaithersburgh, MD, USA) and XL-1 Blue (Stratagene) were used for DNA cloning and screening experiments.

The Saccharomyces cerevisiae phosphatase mutant strain YHH-33 ( his3-11,15; leu2-3,112; pho5) was kindly supplied by Dr. Meyhack (Ciba-Geigy, Basel, Switzerland). Stock cells were maintained on solid Yeast Nitrogen Base (YNB) medium containing the amino acids necessary for complementation. Transformed cells were plated on defined YNB medium without leucine (complementation present in the 181A1NE vector).

PCR AMPLIFICATION OF THE PHO 5 GENE FROM Saccharomyces cerevisiae

Genomic yeast DNA was isolated according to Rose et al. (1990) and used as a template in the PCR reactions to amplify the DNA sequence coding for the mature PHO5 enzyme. The reactions were done in a Perkin Elmer Cetus thermocycler using PHO1 (5´-GCTAGGATCCGGTACCATTCCCTTAGGCAAACTAGCC) and PHO2 (5´-GCTAAGATCTTTATTGTTTTAATAGGGTATCA) as forward and reverse primers, respectively. The former was complementary to the 5´-end of the pho5 gene coding region, without the PHO5 start codon and signal sequence. Primer PHO2 was complementary to a stretch of 38 bp including the pho5 stop codon. Both primers introduced additional restriction sites at the ends of the amplified DNA ( BamHI for primer PHO1 and BglII for primer PHO2). The following temperature profile (40 cycles) was used for amplification: denaturation, 94°C/2 min; primer annealing, 50°C/1.5 min; primer extension, 72°C/ 2.5 min.

CONSTRUCTION OF THE SIGNAL SEQUENCE TRAP (SST) VECTOR (PSDEP-0)

For construction of the SST vector, the coding region of the yeast pho5 truncated gene obtained by PCR was inserted into the E. coli/yeast shuttle vector 181A1NE (Riesmeier et al. 1992). DNA sequence analysis confirmed the presence of the yeast pho5 gene coding region. Expression of the PHO5 in this vector is driven by the constitutive alcohol dehydrogenase promoter recognized by the yeast transcription machinery. To cover all possible frames in clones coming from the cDNA library, two other vectors were also constructed containing one (pSDEP-1) and two (pSDEP-2) extra nucleotides (adenine) after the BamHI site in the original vector pSDEP-0.

BACTERIA AND YEAST TRANSFORMATION

E. coli were transformed according to Hanahan (1993). Yeast transformation was done as described by Dohmen et al. (1991), with minor modifications. After transformation, the yeast cells were grown for 3-4 days at 28°C prior to staining.

STAINING OF YEAST COLONIES AND SPECTROPHOTOMETRIC DETERMINATION OF ACID PHOSPHATASE ACTIVITY

The yeast colonies were stained for acid phosphatase activity as described by Dorn (1965) and To-E et al. (1973), with the addition of agarose (final concentration, 0.5%) to avoid dislodging the colonies on the plate. Positive colonies remained viable for up to 30 min after the reaction and could be inoculated in liquid media for further analysis. Acid phosphatase activity was also determined spectrophotometrically (Sidhu and Bollon 1987).

SCREENING FOR PHO5 ACTIVITY

After transformation with plasmids containing unknown sequences inserted in front of the truncated pho5 in vectors pSDEP-0, 1, and 2 as described above, aliquots of yeast cells were plated on minimal selective medium. The cells were grown as described and the staining solution was dropped on the colonies. After ten minutes red-colonies were detectable with the naked-eye. About 2000 colonies of transformed cells per plate were usually obtained by plating 20-50 µL aliquots.

ISOLATION OF CDNA 5´- ENDS VIA PCR AND CONSTRUCTIONS OF A SIGNAL SEQUENCE SS-VECTOR LIBRARY

An oriented lZAPII cDNA library previously established from potato leaf epidermal fragments highly enriched for guard cells (Kopka et al. 1997) was used as a source to clone genes from novel proteins destined for the secretory pathway. Complementary DNA fragments contained a NotI restriction site at their 5´-end and a XhoI restriction site at their 3´-end. Considering that signal sequences are located at the 5´-end of genes coding for membrane and secreted proteins, an enrichment for these sequences was obtained prior to inserting the sequences in front of the truncated pho5 gene. PCR reactions were done with T3 as the forward primer and a set of four degenerated oligonucleotides as reverse primers, each one 10 bases long and containing a Sau3A ( BamHI compatible) restriction site at their 3´-end (SST1, 5´-CATGGWGATC; SST2, 5´-CAGTCWGATC; SST3, 5´-CAGTASGATC and SST4, 5´-CAGTTSGATC). The primers were designed to anneal randomly to internal regions of genes in the library and contained one wobble site (W or S) to increase the variability of the combination. Alternatively, T3 and T7 were used as forward and reverse primers, respectively. After gel electrophoresis, the smear of fragments obtained was eluted and digested with NotI and Sau3A separately. With the latter restriction enzyme, reaction aliquots were withdrawn at different incubation times to provide greater variability in the fragment sizes. The digested fragments were ligated to the truncated yeast phosphatase in the pSDEP shuttle vectors 0, 1, and 2, and used for E. coli transformation to produce the signal sequence SS-vector library. All transformed cells were recovered by carefully harvesting the colonies grown on solid media and aliquots of a DNA maxi-preparation from these cells were used to transform yeast mutant cells prior to screening for PHO5 activity.

SCREENING FOR FULL-LENGHT CLONES USING THE l ZAPII CDNA LIBRARY

Approximately 5 x 10⁵ plaque-forming units of a l ZAPII cDNA library established from potato leaf epidermal fragments were screened using the sequences retrieved in front of the truncated pho5 gene as probes. Radioactive labeling with (a -³²P)dCTP (Amershan) was done using a random prime labeling kit from Boehringer Mannheim. Filters were hybridized overnight at 42°C in 250 mM sodium phosphate buffer (pH 7.2) containing 7% SDS, 1% BSA and 1 mM EDTA, and washed at 42°C in 5 x SSC, 0.5% SDS, 5% formamide (20 min) and in 3 x SSC, 0.5% SDS (10 min). Plaque-purified phages were converted to pBluescript^® SK derivatives by excision in vivo using the helper phage Exassist, according to the protocol provided by the manufacturer (Stratagene). Rescued phagemids were investigated by restriction analysis and DNA sequencing.

SEQUENCE ANALYSIS

DNA sequences were determined by the dideoxy method (Sanger et al. 1977).

NORTHERN BLOT ANALYSIS

Potato plants grown in a greenhouse were used as a source of RNA. The plant material was frozen in liquid nitrogen and total RNA was extracted according to Logemann et al. (1987). RNA from epidermal fragments highly enriched for guard cells was obtained as previously described (Kopka et al. 1997). RNA gel electrophoresis and northern blot analysis were done as described elsewhere (Landschütze et al. 1995). Membranes were washed at 50°C in 3 x SSC, 0.5% SDS (15 min), followed by 1 x SSC, 0.5% SDS (10 min).

POTASSIUM CHANNEL (KST1) PARTIAL SEQUENCES INSERTED in frame TO THE PHO5 GENE AS A MODEL FOR THE CARACTERIZATION OF PHOSPHATASE ACTIVITY RELATIVE TO ITS POSITION IN THE CELL MEMBRANE

Partial sequences of the inward rectifying K⁺ channel KST1 (Müller-Röber et al. 1995) were used to construct hybrid clones with the truncated acid phosphatase gene in the yeast vector for further characterization of PHO5 activity. Four clones were constructed, two positioning PHO5 inside the cell, and two positioning the enzyme outside the cell, depending on the number of intermembrane domain sequences inserted in front of pho5. The first 260 nucleotides located at the 5´-end of the KST1 clone (probably responsible for coding its signal sequence) and the signal sequence plus the first intermembrane domain from the spinach sucrose transporter were inserted in frame to the pho5 gene for comparison of the PHO5 activity in vivo. Yeast cells were transformed with the different constructs and plated as usual.

3. RESULTS

Prior to screening for secreted PHO5 directed by sequences from the cDNA library, the activity of the extracellular acid phosphatase coded by the sequence obtained by PCR with primers PHO1 and PHO2 was tested by fusing a 200 bp sequence containing the probable signal sequence of the sucrose transporter cloned from spinach (Riesmeier et al. 1992). This construction, referred to as 181A1NE-STSS-PHO5, served as a positive control. The presence of characteristic red yeast colonies after staining showed that this 200 bp fragment mimicked the original PHO5 signal peptide and led to the secretion of an active acid phosphatase by the yeast cell (Figure 1A). A five-minute preincubation of the yeast colonies with 0.1 M sodium fluoride (an inhibitor of acid phosphatases) at pH 6.7 inhibited the staining, thus confirming the involvement of an acid phosphatase in the reaction (data not shown).

That signal sequences other than those directing a polypeptide through the default pathway would not be detected by this model system was ascertained by fusing sequences in front of a truncated pho5 which could not lead the protein to the membrane or to the outside of the cell. Thus, the ~ 99 bp Asp718/ BamHI fragment encoding the transit peptide of the potato mitochondrial matrix processing peptidase (Braun et al. 1992, Landschütze 1995), the ~ 300 bp Asp718/ BamHI fragment encoding the transit peptide of the potato plastidic ADP-glucose pyrophosphorylase large subunit (Müller-Röber et al. 1990), and the ~ 200 bp NotI/ BamHI fragment containing the 5´-end of the potato cytosolic phosphoenolpyruvate carboxylase (La Cognata 1996) were substituted for the sucrose transporter signal sequence in the vector 181A1NE-STSS-PHO5. As expected, none of these produced a positive red staining for acid phosphatase (data not shown).

The signal sequence SS-vector library (see "Materials and Methods'') containing the putative 5´-end regions from the guard cell cDNA library inserted in front of the truncated pho5 reporter gene was used to transform YHH-33 mutant cells. After growing and screening for PHO5 activity, two colonies were isolated (clones YE139 and YE290), grown in liquid selective medium and replated for a second staining which was necessary to confirm and properly isolate the potential positive clone. These two sequences are indicated below.

CLONE YE139

5´- T ATT GTT TCT AAT TTT TTC CTA AAA TAA GCT AAG GCA ATT TAC CAC TCT TCA ATC ATA TCT GCA TCT GTT CTA TAT TGG TAT TGA GGT TCT GCC ATG ACA TTG TAC GGA CAA GCC ATC TTT CTG GGT TTC TTG ATC CTT pho5 -3´

This sequence shows one start codon (underlined ATG) in frame to the pho5 gene that served as an initiation codon and provided a signal sequence for PHO5 to reach the extracellular milieu. Before screening the guard cell cDNA library, a northern blot using RNA isolated from different potato tissues was done using this fragment as a probe to assure that the sequence came from the library and was not a PCR artifact. The result would also indicate the size of the original gene to be searched for in the library and thus, the size of the protein encoded. As depicted in Figure 1B, the highest levels of expression were found in green buds and stems, with considerable expression in roots and sink leaves. The full-size gene containing the sequence above would be about 3.5 kbp long.

A sequence containing about 3.6 kbp was retrieved after screening the guard cell cDNA library with clone YE139. Sequencing and restriction pattern analysis indicated a chimaeric clone, with the first 1.5 kbp corresponding to an unknown protein and its second half to the 3´-end of plant cytochrome P450. As expected, the sequence from clone YE139 was found at the 5´-end of this unknown clone, indicating that it was responsible for encoding the signal sequence from this protein. Transforming YHH-33 yeast mutant cells again with YE139 confirmed the positive staining for acid phosphatase activity.

CLONE YE290

5´- TT CCA TTC AGT TTC CTT TAC TTG ATC GAA CAG CCC CAA ATT CAG TTA TTT CAA CTA CAT TAA ATG ATC TTT CAA ATT GGT CAA GAC TCT CTA GTT TAT GGC CGC TTC TCT ATG GTA CCA GTT GTT GCT TCA TTG AAT TTG CTT CAC TAA TAG GCT CAC GCT TCG ACT TT*G ATC* CTG ATG AGC GTT TCT TCG TGG ATT TTC GGG GTT TTG TTA GCT GGA ATA TGC AGT AGT GAT AAA CCC TAT ATG GAA CTG AGG AAA TCA GCT GAA TTG TTT GAT GAT TCT TTG ATC CTT pho5 -3´

This is a chimaeric sequence. The Sau3A cleavage site indicated between two asterisks marks the probable limits of two sequences after comparative analysis with known sequences in the Genebank. The upstream sequence showed homology to a plastidic protein, whereas the downstream sequence showed no significant homology to any known protein. One of the two start codons after this cleavage site and in frame to the truncated pho5 gene could be responsible for the enzyme secretion. The second half of this clone was amplified by PCR and cloned into pBluescript^® SK. Northern blot using this sequence as a probe indicated a 3 kbp gene being differentially expressed primarily in floral parts (androceum and gyneceum) and roots (Figure 2). Significant expression could also be observed in green buds and epidermal fragments.

A sequence of about 720 bp and containing part of the sequence used as a probe was retrieved after screening the cDNA library again. This sequence also showed no homology to known proteins.

Because of the low efficiency in recovering potential sequences other than chimaeric ones directing PHO5 to the outside of the cell, we examined whether extracellularly located but membrane-bound PHO5 would interact with the staining reagents and give a positive result, or whether PHO5 must be sterically free to provide positive staining. Hybrid genes were constructed coding for one or more transmembrane domains from the inward rectifying K⁺ channel KST1 fused in frame to the truncated pho5, thereby positioning the acid phosphatase to the cell interior or exterior. After transformation and growth, none of the supposedly positive clones (those expressing PHO5 bound to the outside of the cell) showed the expected red staining. In contrast to the positive staining obtained with the signal sequence from the spinach sucrose transporter, the construct encoding only the probable signal sequence from KST1 in frame to the phosphatase did not stain red. However, all transformants showed positive acid phosphatase activity after cell disruption compared to the low activity obtained with YHH-33 mutant cells containing the vector without insert (Figure 3). Another hybrid protein was constructed using the spinach sucrose transporter. Here, in addition to the signal sequence, the first transmembrane domain sequence was also cloned in frame to the acid phosphatase gene. This was expected to produce a hybrid protein in which PHO5 would face the outside of the cell. Again, no acid phosphatase activity was detected by direct staining of the colonies, although activity was seen after disruption of the cells (Figure 3).

4. DISCUSSION

The functionality of the SST-system was demonstrated by inserting the signal sequence from a known membrane protein (sucrose transporter from spinach) and later by retrieving two unknown sequences from a guard cell cDNA library showing strong tissue-specific expression.

Among the various problems encountered during the development of the SST-system, the recombination of fragments obtained after NotI and Sau3A digestion, and the formation of chimaeric sequences as a consequence of such recombinations, were unsolved. The chimaeric sequences were produced by linking fragments of different sizes containing the Sau3A cleavage site at both ends, so that the final product would have a NotI site at the 5´-end, as expected, followed by many shorter sequences of joined Sau3A- Sau3A fragments.

An attempt to improve the yield of non-chimaeric sequences involved the use of a biotinylated T3 as a 5´-end primer for the generation of PCR fragments, together with T7, a mixture of degenerated 10mers as described in "Materials and Methods'', or primers containing only a BamHI cleavage site at their 3´-end. The PCR fragments thus obtained were cleaved with Sau3A and aliquots were withdrawn after different incubation periods. These aliquots were treated with streptavidin-coated beads, so that fragments with only one Sau3A cleavage site at their 3´-ends would be retained. These fragments would then be retrieved by washing the beads with appropriate buffers, and further cleavage with NotI would give the expected NotI- Sau3A fragments to be cloned in front of the pho5 gene in the vector pSDEP. Since this procedure resulted in a dramatic decrease in the number of yeast colonies grown after transformation (only 2-6 colonies/plate), these experiments were discontinued. None of the modifications introduced resulted in the exclusive insertion of 5´-ends originating from single cDNA clones. Although other sequences retrieved from the cDNA library also led to the secretion of acid phosphatase, for most of these it was not possible to demonstrate exactly which segment was responsible for the secretion, because of the high recombination rates for sequences containing Sau3A restriction sites at both ends and the consequent formation of chimaeras. As shown elsewhere, up to 25% of randomly generated peptides can function as signal sequences for the ER, mitochondria, and bacterial plasma membrane (Schatz and Dobberstein 1996). Interestingly, the sequence of the 5´-end region of b -lactamase was also retrieved after screening for PHO5 activity and probably resulted from digestion of the shuttle vector used during cloning.

Further experiments using the potassium channel KST1 gene as a model revealed other uncertainties not considered at the beginning of this work. Among these, that the position of the acid phosphatase relative to the cell membrane might play a decisive role in its catalytic activity and influence the detection of positive clones. A similar effect caused by immobilization of lipase on the surface of yeast cells has already been described (Schreuder et al. 1996). When the acid phosphatase was linked to the plasma membrane via one or more transmembrane domains of the KST1 protein, its enzymatic activity was detected only in extracts of these cells. These findings were corroborated by comparing the enzymatic activity of acid phosphatase fused to the spinach sucrose transporter signal sequence free in the periplasmic space, which was positive, with the activity of an enzyme anchored in the plasma membrane by one of its transmembrane domains, which gave negative staining. That the probable signal sequence from KST1 was not able to direct the acid phosphatase to outside the cell was a surprise, but not necessarily unexpected. It may be argued that while the general mechanisms of signal sequence recognition between yeast ( S. cerevisiae) and plants ( S. tuberosum) are basically the same, there are subtle variations. Thus, the position of acid phosphatase relative to the cell membrane, and signal sequence recognition among different eukaryotes could have affected the retrieval of positive clones, even if chimaeric sequences were not the main problem.

Other reports have described signal sequence traps (Skarnes et al. 1995, Yokoyama-Kobayashi et al. 1995), but only one (Klein et al. 1996) has yielded few drawbacks. The excellent results obtained by Klein and coworkers probably reflected the fact that their system involved only mutant complementation on a selective medium rather than a direct screening procedure. Although PHO5 yeast mutants were used in our system, the screening involved staining as well as mutant complementation. Besides, those authors used a human cDNA library for constructing the vectors for the transformation of yeast cells.

These and other differences in the ability of yeasts in handling plant and animal proteins may account for some of the variations reported in signal sequence trap studies.

ACKNOWLEDGMENTS

The authors thank R. Breitfeld, B. Burose, and T. Mieland for caring for the greenhouse plants, and A. Voigt and J. Bergstein for photographic work. M. J. S. was the recipient of a doctoral fellowship from CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico, Brazil). Part of this work was supported by a Deutsche Forschungsgemeinschaft grant to B. M.-R.

RESUMO

O direcionamento de proteínas a organelas e à membrana celular, ou de proteínas a serem secretadas, é coordenado por seqüências sinalizadoras localizadas na extremidade 5´ de seus respectivos genes que codificam peptídeos-sinal. Este trabalho analisa um sistema para seleção de seqüências sinalizadoras utilizando uma fosfatase ácida de levedura, enzima reconhecidamente secretada por estes organismos, desprovida de seu códon de iniciação e de sua seqüência sinalizadora, como gene repórter. Uma fração enriquecida em fragmentos provenientes da região 5´ de uma biblioteca de cDNA de células-guarda de batata foi inserida in frame ao gene truncado da fosfatase ácida em vetores apropriados. Após a transformação em leveduras, a atividade da fosfatase ácida foi medida diretamente sobre colônias crescidas em meio seletivo. A seqüência nucleotídica dos prováveis peptídeos-sinal capazes de direcionar aquela enzima ao exterior celular foram utilizadas como sondas para recuperação da seqüência original da biblioteca de cDNA. Dois clones sem homologia conhecida, mas apresentando forte expressão tecido-específica, foram obtidos, um deles (YE139) com expressão acentuada em botões florais verdes e células do tronco, e o outro (YE290) de expressão elevada em androceu, gineceu e raízes. Os diversos problemas encontrados durante a execução do trabalho são discutidos face aos resultados obtidos com outras proteínas-modelo.

Palavras-chave: seqüências sinalizadoras, canal de potássio, fosfatase ácida de levedura, triagem de biblioteca de cDNA.

Correspondence to: Marcelo J. Surpili

Laboratório Nacional de Luz Síncroton, LNLS

Rua Giuseppe Máximo Scolfano, 10.000

Cx. Postal 6192, 13084-971, Campinas, SP, Brazil

E-mail: [e-mail]

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Publication Dates

• Publication in this collection
  24 Jan 2003
• Date of issue
  Dec 2002

History

• Accepted
  31 July 2002
• Received
  15 Mar 2002