Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1992-5-26
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59212, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59213, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59214, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59215, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59216, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59217, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59218, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59219, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59220, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59221, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59222, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59223, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59224, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59225, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59228, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59230, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59231, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59232, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59233, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59234, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59235, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X59236
pubmed:abstractText
LINE-1 (L1) is a mammalian family of highly repeated DNA sequences that are members of a class of transposable elements whose movement involves an RNA intermediate. Both structural and evolutionary data indicate that the L1 family consists of a small number of active transposable elements interspersed with a large number of L1 pseudogenes. In the mouse, the longest, characterized L1 sequences span about 7000 base-pairs and contain two long open reading frames. Two subfamilies of mouse L1 elements, A and F, have been defined on the basis of the type of putative transcriptional regulatory sequence found at the 5' end. In order to identify a transcribed subset of L1 elements in mouse F9 teratocarcinoma cells, we have examined the strand-specificity of L1 transcription by Northern analysis and compared the open reading frame-1 sequences of ten A-type cDNAs with fifteen genomic A-type L1 elements. Transcripts containing A-type sequence are far more abundant than those containing F-type sequence. Although the majority of L1 RNA in F9 cells appears to be transcribed non-specifically from both strands, our results provide evidence for a subpopulation of variable length, strand-specific transcripts arising from A-type transcriptional regulatory sequences. F9 cell cDNA sequences, which share greater than 99.5% sequence identity with one another, represent a homogeneous subset of the genomic L1 population. Examination of genomic mouse L1 sequences reveals three types of length polymorphism in a defined segment of the first open reading frame. Phylogenetic analysis shows a correlation between the type of length polymorphism in the first open reading frame and the relative age of an individual A-type genomic L1 element. Comparison of the cDNA and genomic sequences indicates that the youngest subgroup of A-type L1 elements is preferentially transcribed in F9 cells. This subgroup may be currently dominating the L1 dispersal process in mice.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0022-2836
pubmed:author
pubmed:issnType
Print
pubmed:day
5
pubmed:volume
224
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
559-74
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed:year
1992
pubmed:articleTitle
Strand-specific LINE-1 transcription in mouse F9 cells originates from the youngest phylogenetic subgroup of LINE-1 elements.
pubmed:affiliation
Department of Microbiology and Immunology, University of North Carolina, Chapel Hill 27599.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.