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C O M M E N T

Viral IL-6 l i n k e d t o c a n c e r ? now observed that the stromal cells infect the actual cells that become
ultiple myeloma (MM) is a in the bone marrow of M M patients cancerous, M M may provide an
M common form of cancer in
which plasma cells in the bone
are infected with KSHV. Surpris-
ingly, KSHV is only found in the
example of how a viral infection
of one cell type (bone marrow
marrow begin to proliferate un- bone marrow stromal cells and stromal cells) leads to the malig-
controllably. Little is known about does not appear to infect the plas- nant transformation of another
the factors leading to MM, but one ma cells directly. As KSHV seems cell type (plasma cells becoming
cytokine, interleukin-6 (IL-6), has to be absent from the bone marrow plasmacytomas).
been identified as a potent growth of healthy individuals or patients
factor for myeloma cells. A recently with other malignancies, infection Rettig, M.B. etal. (1997) Kaposi's sar-
with KSHV and the production of coma-associated herpesvirus infection
identified virus, Kaposi's sarcoma-
of bone marrow dendritic cells from
associated herpesvirus (KSHV), viral IL-6 may play a causative multiple myeloma patients, Science
encodes a viral form of IL-6 that is role in M M by transforming nor- 276, 1851-1854
homologous to the human form mally quiescent plasma cells into
and also demonstrates similar bio- plasmacytomas. In contrast to Mark Slifka
logical activity. Rettig et al. have other oncogenic viruses, which e-mail: mslifka@scripps.edu

TTO

m TECHNICAL TIPS ONLINE


http://www.elsevier.com/Iocate/tto http://www.elsevier,nl/Iocate/tto (in Europe)

New Technical Tip articles published recently in Technical Tips Online include:

Spyropoulos, B., Heng, H.H.Q. and Moens, P.B. (1997) Granger, B.L. (1997) A glass bead method for picking
Recycling cells in FISH and immunocytology studies bacterial colonies T01175
T01090
Law, D. and Crickmore, N. (1997) Use of a simplified
Memelink, J. (1997) Two yeast/Escherichia and rapid size screen protocol for the detection of
coil X/plasmid vectors designed for yeast one- and recombinant plasmids T01172
two-hybrid screens that allow directional cDNA
cloning T01111 Lazik, A. et al. (1997) A method for preparing
Dil-labeled tissue that allows single-cell resolution
Speleman, F. et al. (1997) Improved protocol for with conventional epifluorescence microscopy
chromatin fibers from fixed cells T01123 T01119
Parkinson, N. et al. (1997) An inverse PCR strategy Cho, C., Myles, D.G. and Primakoff, P. (1997) A PCR
for the recovery of end fragments from the pRML YAC method for distinguishing cells from mouse strains
vector T01169 129 and C57BL/6 for gene knockout studies T01139

Editor Adrian Bird, Institute for Cell and Molecular Biology at the University of Edinburgh

October issue: H o w to sequence a small genome


A poster f r o m Trends in Microbiology a n d Trends in Genetics
by Claire Fraser a n d colleagues at the Institute of G e n o m i c Research.

Recent technical advances have led to an exponential rise in the number of small genomes being completely
sequenced. This poster aims to highlight the key steps required to resolve small genomes, from random sequencing
to microarray analysis.

Copyright© 1997ElsevierScienceLtd.Allrightsreserved.0966 842X/97/$17.00

TRENI)S IN MICROBIOLO(]Y 342 voL 5 N o . 9 SEPTEMBER 1 9 9 7

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