Cloning of Tetrahymena Genomic Sequences Whose Message Abundance is Increased During Conjugation
Document Type
Article
Language
eng
Format of Original
8 p.
Publication Date
1-1989
Publisher
Elsevier
Source Publication
Developmental Biology
Source ISSN
0012-1606
Abstract
A molecular and biochemical inquiry into protein regulation during Tetrahymena thermophila conjugation was carried out in two ways: a two-dimensional gel analysis of newly translated proteins and the molecular cloning of genes whose message abundance is increased. The two-dimensional gel analysis indicated that the synthesis of 32 predominantly basic proteins was stimulated in conjugating cells. The induction of these proteins could not be correlated with length of starvation or with mating type. The transcription pattern and molecular organization of three clones of T. thermophila genomic DNA, selected on the basis of differential hybridization to conjugating or control cell RNA, were investigated. Two of the clones, which were homologous to transcripts detected in conjugating cells, showed no rearrangements between micro- and macronuclear DNA. A third clone was divided into three segments. One segment was homologous to sequences limited to the micronucleus. A second segment hybridized to a large number of restriction fragments of micronuclear DNA digested with HindHI but to only two fragments of macronuclear DNA. A third segment, which was complementary to one transcript in conjugating cells and to two different transcripts in control cells, hybridized to two fragments in micronuclear DNA and one fragment in macronuclear DNA.
Recommended Citation
Rogers, Melissa B. and Karrer, Kathleen M., "Cloning of Tetrahymena Genomic Sequences Whose Message Abundance is Increased During Conjugation" (1989). Biological Sciences Faculty Research and Publications. 177.
https://epublications.marquette.edu/bio_fac/177
Comments
Developmental Biology, Vol. 131, No. 1 (January 1989): 261-268. DOI.
Kathleen Karrer was affiliated with Brandeis University at the time of publication.