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Polymerase chain reactions with alphoid‐repeat primers in combination with Alu or LINEs primers, generate chromosome‐specific DNA fragments
Author(s) -
ERICKSON R. P.,
GLOVER T. W.,
HALL B. K.,
WITT M.
Publication year - 1991
Publication title -
annals of human genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.537
H-Index - 77
eISSN - 1469-1809
pISSN - 0003-4800
DOI - 10.1111/j.1469-1809.1991.tb00414.x
Subject(s) - biology , microbiology and biotechnology , dna , polymerase chain reaction , alu element , genetics , dna sequencing , dna polymerase , gene , genome , human genome
SUMMARY Y alphoid primers in combination with Alu and LINEs primers generated new DNA fragments in polymerase chain reactions (PCR) on DNA from a Y‐only somatic cell hybrid but not from X‐only, 3‐only, or 21‐only hybrids. X alphoid primers used in a similar manner generated new DNA fragments from the X‐only hybrid, and 1 of the primers (X 2 ) also generated new DNA fragments on 3‐only and 21‐only hybrids when used in conjunction with Alu or LINEs primers. In all but one case, consensus alphoid primers generated new chromosome‐specific fragments in PCR reactions with the Alu or LINEs primers. A search for cryptic Alu‐ or alphoid‐alone PCR products as the source for one Alu ‐alphoid band (chosen at random) was negative. Partial sequencing of products demonstrated that alphoid and Alu sequences were indeed contiguous in some newly synthesized DNA fragments. While Alu or LINEs primers generate smears of DNA fragments on total human DNA, the alphoid‐nonalphoid repeat combinations generated electrophoretically distinguishable bands of DNA when the template was total DNA. While these were distinguishable with different chromosome‐specific alphoid primers, the DNA fragments were not of the same sizes as those generated with the chromosome‐only hybrids.