It is one of those important aims in the new 5-year plan of the human
genome research project([1]) to construct the STS with the resolution
at 100 kb. Thus it requires about 30 000 new STS to cover the whole ge
nome. In 1989, Olson([2]) first proposed the concept of STS and STS ma
pping. Since then STS map has been considered to be one kind of framew
ork maps for landmark. STS are single copy sequences with the lengths
of several hundreds of base pairs. Their sequences are known; their po
sitions are determined, and they can be specifically amplified by PCR
in the presence of the total genome DNA. STS map is very special, and
it is quite different from other physical maps. Restriction endonuclea
se map is marked by cleavage signals, but there are too many such kind
s of signals on the whole genome; Alu-PCR finger-printing map also giv
es out vague results. For a single STS, it is a unique copy in the who
le genome. When two YACs or Cosmids involve the same STS, they must be
contiguous. The YAC contigs of the long arm of the 21st chromosome an
d Y chromosome have been constructed by the STS mapping method. We onc
e reported a single copy sequence library with 1 075 single copy seque
nces([3]). After its sequences were confirmed to be new, its localizat
ions were decided by FISH, and its appropriate PCR amplification condi
tions were set up; a new STS was constructed.; Here we report an STS f
rom X chromosome. and