The Telomere and Telomerase: Nucleic Acid--Protein Complexes Acting in a
Telomere Homeostasis System. A Review
E. H. Blackburn1
1Department of Microbiology and Immunology and Department of
Biochemistry and Biophysics, University of California, 513 Parnassus,
Room S447, Box 0414, San Francisco, CA 94143-0414, USA; fax: (415)
476-8201; E-mail:
porter@itsa.ucsf.edu
Submitted August 12, 1997.
The tandemly repeated DNA sequence of telomeres is typically specified
by the ribonucleoprotein enzyme telomerase. Telomerase copies part of
its intrinsic RNA moiety to synthesize one strand of the telomeric
repeat DNA. Recent work, taken together with many observations over the
past years, has led to the concept of a telomere homeostasis system. We
have analyzed the interplay between two key physical components of this
system: structural components of the telomere itself and of telomerase.
Here we review some of these recent studies. The experimental method
used in common in these studies was to make mutations in the template
sequence of telomerase RNA, which caused various phenotypes. First,
mutating specific residues in the ciliate Tetrahymena
thermophila and yeast showed that these residues are required for
critical aspects of the enzymatic action of telomerase. Second, certain
mutated telomeric sequences caused a strong anaphase block in
Tetrahymena micronuclei. Third, specific template mutations in
the telomerase RNA gene led to varying degrees of telomere elongation
in Tetrahymena and the yeast Kluyveromyces lactis. For
some of the K. lactis mutations, the loss of length unregulated
elongation was directly related to loss of binding to K. lactis
Rap1 protein. Using K. lactis carrying alterations in the
telomerase RNA template, and in the gene encoding the Rap1 protein, we
found that a crucial determinant of telomere length homeostasis is the
nature of the duplex DNA--Rap1 protein complex on the very end repeat
of the telomere. We propose that this complex plays a key role in
regulating access of telomerase to the telomere.
KEY WORDS: telomeres, telomerase, homeostasis of telomere
lengths, Rap1 protein.