RECOMBINATION BY SEQUENCE REPEATS WITH FORMATION OF SUPPRESSIVE OR RESIDUAL MITOCHONDRIAL-DNA IN NEUROSPORA

被引:31
作者
ALMASAN, A [1 ]
MISHRA, NC [1 ]
机构
[1] UNIV S CAROLINA,DEPT BIOL SCI,COLUMBIA,SC 29208
关键词
RECOMBINATION HOT SPOTS; ILLEGITIMATE RECOMBINATION; POLYMERASE CHAIN REACTION;
D O I
10.1073/pnas.88.17.7684
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recombination junctions of several Neurospora mitochondrial DNA (mtDNA) mutants and their revertants were identified. Their nucleotide sequences and putative secondary structures were determined in order to understand the nature of the elements involved in intramolecular recombination. Multiple deletions, involving the same portion of Neurospora mtDNA, were identified in six independently isolated mutants. A 9-nucleotide repeal element, CCCCNCCCC, was found to be involved in these and other Neurospora mitochondrial recombination events. The repeat elements were clustered as hot spots on the Neurospora mtDNA and were associated with palindromic DNA sequences. The palindromes have a potential to generate hairpin structures. A much lower free energy of the putative hairpins at the 5' end of the recombination site, and the possible formation of non-B-DNA structure by polypyrimidine tracks, may be important in the initiation of recombination. Using PCR, we found low levels of a specific mitochondrial deletion in certain Neurospora mutants. Their presence in low amounts in a population with a much larger number of normal mtDNA is unexpected. Contrary to earlier belief, this finding supports the view that deleted, smaller DNA molecules are not always suppressive relative to normal mtDNAs.
引用
收藏
页码:7684 / 7688
页数:5
相关论文
共 44 条
[31]  
RAND DM, 1989, GENETICS, V121, P551
[32]   DNA SEQUENCING WITH CHAIN-TERMINATING INHIBITORS [J].
SANGER, F ;
NICKLEN, S ;
COULSON, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5463-5467
[33]   A DIRECT REPEAT IS A HOTSPOT FOR LARGE-SCALE DELETION OF HUMAN MITOCHONDRIAL-DNA [J].
SCHON, EA ;
RIZZUTO, R ;
MORAES, CT ;
NAKASE, H ;
ZEVIANI, M ;
DIMAURO, S .
SCIENCE, 1989, 244 (4902) :346-349
[34]   MOLECULAR STUDIES OF DELETIONS AT THE HUMAN STEROID SULFATASE LOCUS [J].
SHAPIRO, LJ ;
YEN, P ;
POMERANTZ, D ;
MARTIN, E ;
ROLEWIC, L ;
MOHANDAS, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (21) :8477-8481
[36]   FRAMESHIFT MUTATIONS AND GENETIC CODE [J].
STREISINGER, G ;
OKADA, Y ;
EMRICH, J ;
NEWTON, J ;
TSUGITA, A ;
TERZAGHI, E ;
INOUYE, M .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1966, 31 :77-+
[37]   EXCISION-AMPLIFICATION OF MITOCHONDRIAL-DNA DURING SENESCENCE IN PODOSPORA-ANSERINA - A POTENTIAL ROLE FOR AN 11 BASE-PAIR CONSENSUS SEQUENCE IN THE EXCISION PROCESS [J].
TURKER, MS ;
DOMENICO, JM ;
CUMMINGS, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 198 (02) :171-185
[38]   CHEMICAL PROBING OF HOMOPURINE-HOMOPYRIMIDINE MIRROR REPEATS IN SUPERCOILED DNA [J].
VOLOSHIN, ON ;
MIRKIN, SM ;
LYAMICHEV, VI ;
BELOTSERKOVSKII, BP ;
FRANKKAMENETSKII, MD .
NATURE, 1988, 333 (6172) :475-476
[39]  
WAHL GM, 1989, CANCER RES, V49, P1
[40]   MITOCHONDRIAL-DNA MUTATIONS AND NEUROMUSCULAR DISEASE [J].
WALLACE, DC .
TRENDS IN GENETICS, 1989, 5 (01) :9-13