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Article Abstract

Background: Genome walking has contributed to life science-related areas. Herein, we detailed a new genome walking method, nominated as arbitrarily suffixed sequence-specific primer PCR (ASP-PCR).

Objectives: This study aimed to construct an efficient random PCR-based genome walking method.

Materials And Methods: The key for this method is the use of a hybrid primer (HP) in primary ASP-PCR. This HP is fabricated by suffixing an arbitrary sequence to outmost sequence-specific primer. The relaxed cycle in primary ASP-PCR facilitates the partial annealing of HP to genome, creating many single-stranded DNAs. In the next stringent cycles, target single-strand is exponentially amplified, because it also has a site complementary to the sequence-specific part of HP; while nontarget cannot be further processed due to lacking such a site. Nested secondary/tertiary ASP-PCR further selectively enriches target DNA.

Results: The practicability of ASP-PCR was confirmed by obtaining unknown DNAs adjacent to gene and CD0817 L-glutamic acid decarboxylase gene. The results showed that each secondary or tertiary ASP-PCR exhibited 1 - 2 clear target amplicon(s) with size from 1.5 to 3.5 kb, and a weak background.

Conclusions: The ASP-PCR is a promising genome walking scheme, and may have a potential use in life science-related areas.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11993238PMC
http://dx.doi.org/10.30498/ijb.2024.449960.3896DOI Listing

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