A simple strategy for improving bird sexing from highly degraded DNA samples
A simple methodology was developed to select new sex-specific primers for bird sexing from degraded and low-quantity DNA sources. The strategy was validated using highly degraded DNA extracted from Giemsa-stained blood smears of common cranes (Grus grus). The new primers allowed the accurate molecul...
| Autores: | , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2019 |
| País: | España |
| Institución: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/194821 |
| Acceso en línea: | http://hdl.handle.net/10261/194821 |
| Access Level: | acceso abierto |
| Palabra clave: | Birds Sex-linked markers Molecular sexing Degraded DNA Real-time PCR Grus grus |
| Sumario: | A simple methodology was developed to select new sex-specific primers for bird sexing from degraded and low-quantity DNA sources. The strategy was validated using highly degraded DNA extracted from Giemsa-stained blood smears of common cranes (Grus grus). The new primers allowed the accurate molecular sexing using (i) a classic approach of PCR followed by agarose gel electrophoresis and (ii) an advanced real-time PCR method. The simplicity, speed and low cost make this methodology a versatile molecular tool for selection of novel markers/primers for bird sex differentiation from complex DNA sources, which can be used as basis or complement in several fields of ornithological research. |
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