The overall objective of this proposal is an understanding of the role and affects of the short, interspersed repeats (SINEs) in the mammalian genome. This also includes a better understanding of the RNA mediated transposition mechanism (retroposition) which spreads them throughout the genome. We will continue to carry out characterizations of the RNA polymerase III promoter of the SINEs and factors that affect its activity. These studies will primarily be carried out on recombinant DNA constructs introduced back into culture cells. We will study the affect of nearby sequences, such as enhancers and RNA polymerase II promoters, on the SINE promoter, and more general factors such as chromatin structure and methylation. A second line of experimentation will involve determination of the affect that the SINEs have on increasing both homologous and illegitimate recombinations in the mammalian genome. These studies will involve introduction of recombinant constructs into cells and assaying for recombination using selection techniques. This will be carried out by making human thymidine kinase minigenes which are defective unless the recombination has occurred. We will sequence specific regions (the thymidine kinase region) in several primate genomes in order to determine the time course of appearance of the Alu family in primates. Analysis of these sequences will show when Alu spread through the genome and whether it is still spreading. It will also answer the question of whether there are mechanisms removing Alu family members, as well as inserting them. Additionally we will analyze site- specificity of the integration of the Alu family sequences. We will make recombinant constructs that allow us to prepare RNA molecules that correspond to proposed intermediates in the retroposition process. We will use these intermediates to test some of the retroposition mechanisms parameters in vitro and eventually within transgenic mice.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Project (R01)
Project #
5R01HG000340-10
Application #
3333473
Study Section
Mammalian Genetics Study Section (MGN)
Project Start
1981-09-01
Project End
1993-06-30
Budget Start
1991-07-01
Budget End
1992-06-30
Support Year
10
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Louisiana State University Hsc New Orleans
Department
Type
Schools of Dentistry
DUNS #
782627814
City
New Orleans
State
LA
Country
United States
Zip Code
70112
Batzer, M A; Rubin, C M; Hellmann-Blumberg, U et al. (1995) Dispersion and insertion polymorphism in two small subfamilies of recently amplified human Alu repeats. J Mol Biol 247:418-27
Kass, D H; Aleman, C; Batzer, M A et al. (1994) Identification of a human specific Alu insertion in the factor XIIIB gene. Genetica 94:1-8
Kim, J; Martignetti, J A; Shen, M R et al. (1994) Rodent BC1 RNA gene as a master gene for ID element amplification. Proc Natl Acad Sci U S A 91:3607-11
Batzer, M A; Alegria-Hartman, M; Deininger, P L (1994) A consensus Alu repeat probe for physical mapping. Genet Anal Tech Appl 11:34-8
Batzer, M A; Schmid, C W; Deininger, P L (1993) Evolutionary analyses of repetitive DNA sequences. Methods Enzymol 224:213-32
Novick, G E; Gonzalez, T; Garrison, J et al. (1993) The use of polymorphic Alu insertions in human DNA fingerprinting. EXS 67:283-91
Perna, N T; Batzer, M A; Deininger, P L et al. (1992) Alu insertion polymorphism: a new type of marker for human population studies. Hum Biol 64:641-8
Deininger, P L; Batzer, M A; Hutchison 3rd, C A et al. (1992) Master genes in mammalian repetitive DNA amplification. Trends Genet 8:307-11
Shen, M R; Deininger, P L (1992) An in vivo assay for measuring the recombination potential between DNA sequences in mammalian cells. Anal Biochem 205:83-9
Batzer, M A; Bazan, H A; Kim, J et al. (1992) Large-scale subcloning of bacteriophage lambda ZAP clones. Biotechniques 12:370-1

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