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Anais da Academia Brasileira de Ciências

Print version ISSN 0001-3765On-line version ISSN 1678-2690

An. Acad. Bras. Ciênc. vol.90 no.1 Rio de Janeiro Mar. 2018  Epub Dec 07, 2017

http://dx.doi.org/10.1590/0001-3765201720160089 

Earth Sciences

Protocol for chromosome-specific probe construction using PRINS, micromanipulation and DOP-PCR techniques

PAULO Z. PASSAMANI1 

CARLOS R. CARVALHO1 

FERNANDA A.F. SOARES1 

1Laboratório de Citogenética e Citometria, Departamento de Biologia Geral, Centro de Ciências Biológicas e da Saúde, Universidade Federal de Viçosa, Av. Peter Henry Rolfs, s/n, Campus Universitário, 36570-900 Viçosa, MG, Brazil

ABSTRACT

Chromosome-specific probes have been widely used in molecular cytogenetics, being obtained with different methods. In this study, a reproducible protocol for construction of chromosome-specific probes is proposed which associates in situ amplification (PRINS), micromanipulation and degenerate oligonucleotide-primed PCR (DOP-PCR). Human lymphocyte cultures were used to obtain metaphases from male and female individuals. The chromosomes were amplified via PRINS, and subcentromeric fragments of the X chromosome were microdissected using microneedles coupled to a phase contrast microscope. The fragments were amplified by DOP-PCR and labeled with tetramethyl-rhodamine-5-dUTP. The probes were used in fluorescent in situ hybridization (FISH) procedure to highlight these specific regions in the metaphases. The results show one fluorescent red spot in male and two in female X chromosomes and interphase nuclei.

Key words: DOP-PCR; FISH; micromanipulation; PRINS

INTRODUCTION

Chromosome-specific probes have been widely used to identify chromosomes and elucidate complex ones (Gribble et al. 2004). These probes have been constructed by flow sorting of whole chromosomes or by microdissection, both involving a subsequent amplification (Thalhammer et al. 2004). However, in flow sorting several hundreds of chromosomes must be selected from suspensions to generate a painting probe (Telenius et al. 1992). Owing to this limitation, microdissection has become a popular method to construct whole-chromosome and region-specific painting probes (Guan et al. 1994). Chromosome microdissection is accomplished by conventional or laser techniques. The conventional approach uses fine extended glass needles for collection of whole chromosomes or subchromosomal regions (Meltzer et al. 1992). In turn, laser microdissection employs a UV-laser microbeam in combination with laser-pressure catapulting (LPC) to isolate and eject the chromosome onto a collection device, speeding up the process (Schermelleh et al. 1999).

After microdissection, different strategies have been used to amplify the DNA sequence of the micromanipulated chromosome, such as degenerate oligonucleotide-primed PCR (DOP-PCR) (Telenius et al. 1992), primer extension preamplification (PEP) (Zhang et al. 1992), linker adaptor-mediated PCR (LA-PCR) (Albani et al. 1993) or multiple displacement amplification (MDA) (Dean et al. 2002). DOP-PCR is the most commonly used technique, owing to its relative rapidity and efficiency. Besides, it can be used for amplification of any kind of chromosomes by means of degenerate primers, which randomly bind to the genome during the initial cycles of low stringency (Zhou and Hu 2007).

However, a limiting factor of these techniques is the need for a relatively large number of copies of the target. In order to decrease this number, Christian et al. (1999) performed a DOP-PCR in situ to increase the amount of DNA associated with the chromosome before the micromanipulation. Although this approach was potentially promising to capture a single chromosome, practically no other studies have been described using this strategy.

Therefore, considering the wide applicability of chromosome-specific probes, the present study aims to describe a modified version of the latter protocol that allows constructing a probe from a tiny region of human X chromosome by means of PRINS and DOP-PCR techniques.

MATERIALS AND METHODS

LYMPHOCYTE CULTURE AND SLIDE PREPARATION

Chromosomes were obtained via human lymphocyte culture initiated from blood of male and female volunteers. Blood collection and procedures for cytogenetic evaluation were performed in accordance with the safety standards and criteria of Ethics in Human Research, Resolution 196/96 of the National Health Council. Under laminar flow, 12 drops of blood were added to 5.0 mL of complete culture medium LymphoGrow™ (Cytogen®) with the aid of a Pasteur pipette. The cultures were incubated at 37ºC with 5% CO2 (Sanyo® MCO-18AC model) for 72 h. Next, 50 μL of Colcemid™ (Sigma-Aldrich®) were added and the cultures were incubated for 15 min at 37°C. The cultures were then centrifuged, the supernatant discarded and the pellet resuspended in 0.075 M KCl solution (pH 6.8), preheated to 37°C for 30 min for hypotonic treatment. Fixation of the material was achieved in methanol: acetic acid (3:1) solution with five changes at 10 min intervals. The fixed material was stored in methanol. Slides were prepared by dripping and air-drying as described by Barch et al. (1997).

In situ AMPLIFICATION

For PRINS, slides containing male metaphases were prepared without the air-drying step and with subsequent washing with ultrapure water to remove the excess of fixative compounds. A final volume of 50 μL of reaction mixture, constituted by 1 U Platinum® Taq DNA Polymerase High Fidelity (Invitrogen®), 1X enzyme-specific reaction buffer (Invitrogen®), 2 mM MgSO4 (Invitrogen®), 200 mM dNTP (Promega®) and 4 mM DOP-primer (5’CCGACTCGAGNNNNNNATGTGG3’ - ITD®), was carefully pipetted onto the slide. The slides were covered with plastic coverslip (22 x 60 mm), sealed with glue and placed in a Mastercycler® Gradient (Eppendorf™) thermocycler containing in situ adapter. The reaction conditions consisted of an initial denaturation step at 95°C for 10 min, followed by 8 cycles at 94°C for 1 min; 30°C for 5 min with a ramp rate of 0.3°C/s to 68°C for 5 min; 12 cycles at 94°C for 1 min; 50°C for 5 min with a ramp rate of 0.3°C/s to 56°C for 5 min; 68°C for 5 min; and final extension at 68°C for 5 min.

MICRODISSECTION

After PRINS, the slides were rinsed in 2X SSC 0.1% Triton X-100 solution and in ultrapure water. They were analyzed under microscope, and the metaphase images were digitized for identification of the X chromosomes before micromanipulation, since the banding procedure was not carried out in this methodology to prevent contamination. After careful identification of the X chromosomes, they were micromanipulated with the aid of glass needles (Femtotips® - Eppendorf™) and a micromanipulator (TransferMan® NK 2 - Eppendorf™) coupled to an inverted phase contrast microscope IX70 (Olympus™) mounted with lens LUCPlanFL N - UIS 2 60X / 0.70 Ph2. Ten fragments of the X chromosomes were microdissected and placed into 0.2-mL microtube containing 2 μL of ultrapure water. The chromosomal fragments were treated with 0.5 mg.mL-1 proteinase K at 37°C for 24 h for complete deproteinization of the chromatin, and the DNA was used as template for probe construction.

TEMPLATE AMPLIFICATION AND LABELING

The micromanipulated fragments were amplified by DOP-PCR with 15 μL of reaction mixture containing 4 mM DOP primer (ITD®), 200 mM dNTPs (Promega®), 2 mM MgSO4 (Invitrogen®), 1 U Platinum® Taq DNA Polymerase High Fidelity (Invitrogen®) and 1X enzyme-specific buffer (Invitrogen®) (adapted from Christian et al. 1999 and Hobza et al. 2004). Amplification was performed in a Mastercycler® Gradient (Eppendorf™) thermocycler under the following conditions: initial denaturation at 95°C for 10 min, followed by 10 cycles at 94°C for 1 min; 30°C for 2 min with a ramp rate of 0.3°C/s to 68°C for 2 min; 30 cycles at 94°C for 1 min; 50°C for 2 min with a ramp rate of 0.3°C/s to 56°C for 2 min; 68°C for 2 min; and final extension at 68°C for 5 min. The reaction products were subjected to electrophoresis in 1.5% agarose gel to verify the quality of the amplified material, and quantitation was performed by spectrophotometry in Nanodrop™ device (Thermo Scientific™). The products obtained by DOP-PCR, which amplified fragments of 200 to 600 bp in satisfactory quantity, were selected for direct fluorescent labeling via another DOP-PCR reaction. For this, the following reaction mixture was used: 4 mM DOP-primer (IDT®), 200 mM dNTP (Promega®), 2 mM MgSO4 (Invitrogen®), 40 mM tetramethyl-rhodamine-5-dUTP (Roche®), 1X enzyme-specific buffer (Invitrogen®), 1 U Platinum® Taq DNA Polymerase High Fidelity (Invitrogen®), and 200 ng of amplified DNA template to a final volume of 50 μL for each reaction. The DOP-PCR reaction was performed in a Mastercycler® Gradient (Eppendorf™) thermocycler under the following conditions: 95°C for 5 min; 25 cycles at 94°C for 1 min; 30°C for 1 min with ramp rate of 0.3°C/s to 68°C for 3 min; and final extension at 68°C for 5 min.

FLUORESCENT in situ HYBRIDIZATION (FISH)

For FISH, the slides containing metaphases obtained from cultured lymphocytes of male and female subjects were used, undergoing a series of pre-hybridization treatments. First, the slides were washed in phosphate buffered saline (PBS) for 5 min under agitation and subjected to ethanol series (70%, 85% and 100% for 5 min each). Next, they were treated with 0.4% RNAse 2 mg.mL-1 diluted in 2X SSC at 37°C for 1 h and rinsed in 2X SSC (three times of 5 min) and PBS (5 min). The slides were incubated in 0.005% pepsin diluted in 10 mM HCl for 10 min at 37°C, washed twice in PBS (2 min each time), post-fixed in fixative solution (2% formaldehyde, PBS, 50 mM MgCl2) for 10 min, washed twice in PBS (2 min each time) and subjected to cold ethanol series (70%, 85% and 100% for 5 min each). Meanwhile, the probes were denatured for 10 min at 99°C in 35 μL of a hybridization mixture containing 50% formamide, 2X SSC, 10% dextran sulfate, 1 μg DNA competitor Human Cot-1 DNA (Invitrogen®) and 200 ng of marked probe. The probes were immediately placed at -20°C, where they remained until the hybridization step. Subsequently, the previously denatured reaction mixture was applied to the slides, which were covered with plastic coverslip (22 x 40 mm) and sealed with glue. The slides and the probe underwent a new simultaneous denaturation step at 75°C for 8 min and hybridization at 37°C for 20 h in a Thermobrite StatSpin® device (Abbott®). The coverslips were carefully removed and stringent washes were performed at 45°C, consisting in three 5-min washes in 50% formamide and 2X SSC (pH 7.0) followed by one wash (5 min) in 2X SSC and one wash (5 min) in 2X SSC 1% Triton X-100. Subsequently, the slides were dehydrated in cold ethanol series (70%, 85% and 100% for 5 min each), counterstained with 50 μL of 5 mM DAPI (4’,6-diamidino-2-phenylindole) for 5 min and sealed with coverslips (24 x 50 mm) in PBS solution.

IMAGE CAPTURE

The slides were analyzed using a BX60 fluorescence microscope (Olympus™) with filters WU (for DAPI) and WG (for rhodamine) and 100X immersion objective. The images were captured directly by a CCD video camera (Olympus DP71™) coupled to a microscope and a computer containing a digitizer board and image analysis software.

RESULTS

The human lymphocyte culture conditions provided metaphases in sufficient number and exhibiting chromosomes morphologically suitable for PRINS, micromanipulation and FISH procedures. The metaphases showed well-spread chromosomes without overlaps, with preserved morphology and different levels of chromatin compaction that enabled distinguishing the homologous pairs. The prepared slides were subjected to PRINS and, after all treatments, the chromosome morphology remained suitable for micromanipulation. At this stage, a portion of the subcentromeric region of ten X chromosomes was microdissected (Figure 1a, b). The fragments amplified by DOP-PCR generated amplification products ranging from 200 to 600 bp. Quantification of the material in Nanodrop™ spectrophotometer (Thermo Scientific™) revealed a DNA amount of 354.2 ng.μL-1, with 260/280 ratio of 1.72.

Figure 1 Microdissection procedure and FISH using chromosome-specific probe obtained via DOP-PCR. Microdissection procedure (a) before and (b) after removal of the chromosome fragment. Probe hybridization in the X chromosome in metaphase of (c) male and (d) female individuals, counterstained with DAPI. Note the red fluorescent spots in the X chromosomes and nuclei. (e) Male and (f) female karyotypes showing the marks on the X chromosomes. (g, h) 3-D plots of the nuclei and sexual pair highlighting the positive signals. Bar = 10 µm. 

After hybridization, the subcentromeric region of a single X chromosome was marked in one chromosome of a male individual metaphase, showing a single corresponding fluorescent signal in interphase nuclei (Figure 1c, e, g). Hybridization in metaphases from a female individual revealed a pair of homologous X chromosomes marked in the subcentromeric region, showing two corresponding fluorescent red spots in interphase nuclei (Figure 1d, f, h). The chromosome labeling was effective in about 95% of the analyzed metaphases.

DISCUSSION

As the chromosomes were not stained, micromanipulation was carried out carefully to collect the same fragment with the same size. Staining was not performed to prevent loss of the fragments amplified by PRINS and to decrease the risk of contamination with exogenous DNA. However, some authors prefer using stained chromosomes to facilitate the identification process (Engelen et al. 1998, Weimer et al. 2001). Another positive aspect of the micromanipulation procedure was that the target chromosome fragments could be easily removed as a result of the rehydration step included before micromanipulation, as described by Engelen et al. (1998). This step was considered important because the fixation and dehydration procedures otherwise keep the chromosomes strongly adhered to the slide, making the capture more laborious (Bussey 1996).

The probe was constructed from only ten small micromanipulated fragments of X chromosomes after amplification by PRINS. Studies have reported the need for large numbers of micromanipulated chromosomes to construct a probe (approximately 20). However, some authors have pointed out that the construction of probes with a lower number of chromosomes is possible (Guan et al. 1994, Engelen et al. 1998, Henning et al. 2008). Christian et al. (1999) described a protocol to generate probes from a single micromanipulated chromosome. As in the present study, these authors used PRINS as strategy to enhance the number of DNA sequence copies and to reduce the required amount of chromosomes to be micromanipulated. Nevertheless, their methodology did not provide repeatability, since no reports reproduced the procedure and not even the authors themselves continued this line of research.

The exposure of the micromanipulated chromosomal fragments to proteinase K is recommended for deproteinization of the chromatin (Weimer et al. 1999). In this study, adequate DNA for amplification was only obtained using proteinase K for 24 h. However, some authors indicate other methods for digestion of proteins. Guan et al. (1994) used the topoisomerase I enzyme for treatment of the microdissected material. Differently, Engelen et al. (1998) performed a procedure employing the temperature as deproteinizing agent, subjecting the material to cycles of 30°C and 50°C.

Amplification using DOP-PCR has been widely employed for probe construction (Christian et al. 1999, Zhou et al. 2001). Still, DOP-PCR conditions must be optimized beforehand to avoid preferential amplification and to generate fragments of 200 to 600 bp, a size range considered effective for probe construction (Hobza et al. 2004). In this sense, it is necessary to improve the time and temperature of annealing and extension for the enzymes. As the latter are highly processive at high temperatures, it is recommended to use the ramp rate between the annealing and extension temperatures (Henning et al. 2008). Another relevant factor in the amplification step is the primer concentration, as limiting primer levels may decrease the amplification rate in the last cycles of the PCR procedure (Czerny 1996). As suggested by Engelen et al. (1998), here we chose to use a higher primer concentration (4 µM) to maintain the high amplification level.

We consider that the FISH procedure was efficient, marking only the chromosome corresponding to that which originated the probe in 95% of the metaphases, without nonspecific signals. Undesired hybridizations were suppressed by the addition of Cot-1, which competes for the repetitive regions of the probe (Craig et al. 1997).

In conclusion, a new methodology was standardized for efficient construction of a chromosome-specific probe using relatively small fragments and low number of DNA copies as template. The described protocol can be used to generate probes for screening of other chromosome regions and analyzing structural and numerical abnormalities. This methodology can be widely applied for many other organisms, not being restricted to human chromosomes.

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Received: February 15, 2016; Accepted: April 15, 2016

Correspondence to: Carlos Roberto Carvalho E-mail: ccarvalh@ufv.br

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