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Sholes, S.

Publications and source records attributed to Sholes, S..

2 recordsLinked to original sources

A mechanism for telomere-specific telomere length regulation

Telomere length is a critical determinant of telomere function and hence chromosome stability. Critically short telomeres induce cellular senescence and division arrest, which eventually may lead to devastating age-related degenerative diseases. Conversely, maintenance of telomere length is a hallmark of cancer. How telomere set-length is established and molecular mechanisms for telomere-specific length regulation remained unknown. Here we detail a mechanism of a telomere-specific set-length regulation that causes drastic differences in telomere length between individual telomeres in the same cell. Indeed, the results show that telomerase recruitment is modulated in cis in a telomere-specific way. Increased Sir4 abundance on yeast TEL03L subtelomeric heterochromatin leads to a set-length maintenance that is two to three times higher than on any other telomere. Remarkably, the distal 15 kb of TEL03L are sufficient to transfer this telomere specific set-length regulation to another chromosome. Furthermore, a mutation in the telomere boundary element protein Tbf1 allows increased Sir4 binding on all telomeres and hence results in longer set-lengths. The results therefore will force a rethinking of telomere length regulation away from the generalized view that all telomeres are treated the same to a more telomere-specific treatment. HIGHLIGHTSO_LIRegulation of the set-length of telomeric repeats is telomere-specific. C_LIO_LITEL03L on yeast chromosome III displays a set-length regulation that confers an extremely long repeat tract. C_LIO_LITransferring the distal part of TEL03L onto chromosome XV is sufficient to impose the very long set-length regulation. C_LIO_LITelomere-specific tract set-length regulation depends on the alternate telomerase recruitment pathway involving Sir4 and yKU and the chromatin boundary protein Tbf1. C_LI GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=122 SRC="FIGDIR/small/598646v2_ufig1.gif" ALT="Figure 1"> View larger version (25K): org.highwire.dtl.DTLVardef@1c3bb52org.highwire.dtl.DTLVardef@13f338forg.highwire.dtl.DTLVardef@51f91aorg.highwire.dtl.DTLVardef@1b95ac0_HPS_FORMAT_FIGEXP M_FIG C_FIG

molecular biology↗

Human telomere length is chromosome specific and conserved across individuals

Short telomeres cause age-related disease and long telomeres predispose to cancer; however, the mechanisms regulating telomere length are unclear. To probe these mechanisms, we developed a nanopore sequencing method, Telomere Profiling, that is easy to implement, precise, and cost effective with broad applications in research and the clinic. We sequenced telomeres from individuals with short telomere syndromes and found similar telomere lengths to the clinical FlowFISH assay. We mapped telomere reads to specific chromosome end and identified both chromosome end-specific and haplotype-specific telomere length distributions. In the T2T HG002 genome, where the average telomere length is 5kb, we found a remarkable 6kb difference in lengths between some telomeres. Further, we found that specific chromosome ends were consistently shorter or longer than the average length across 147 individuals. The presence of conserved chromosome end-specific telomere lengths suggests there are new paradigms in telomere biology that are yet to be explored. Understanding the mechanisms regulating length will allow deeper insights into telomere biology that can lead to new approaches to disease.

molecular biology↗