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                Sp1- and Krüppel-like transcription factors 英文参考文献
                     
Protein family review
Sp1- and Krüppel-like transcription factors
Joanna Kaczynski*?, Tiffany Cook? and Raul Urrutia*?§
Addresses: *Gastroenterology Research Unit, ?Tumor Biology Program, and  §Department of Biochemistry and Molecular Biology, Mayo
Clinic, Rochester, MN 55901, USA. ?Department of Biology, New York University, New York, NY 10003, USA.
Correspondence: Raul Urrutia. E-mail: urrutia.raul@
Published: 3 February 2003
Genome Biology 2003, 4:206
The electronic version of this article is the complete one and can be
found online at /2003/4/2/206
? 2003 BioMed Central Ltd
Summary
Sp1-like  proteins and  Krüppel-like factors  (KLFs)  are highly  related zinc-finger  proteins that  are
important  components  of  the  eukaryotic  cellular  transcriptional  machinery.   By  regulating  the
expression  of a large  number of  genes that  have GC-rich  promoters, Sp1-like/KLF  transcription
regulators  may  take  part  in virtually  all  facets  of  cellular  function,  including  cell  proliferation,
apoptosis,  differentiation, and  neoplastic transformation.  Individual  members  of the Sp1-like/KLF
family can  function as  activators or  repressors depending  on which  promoter they  bind and  the
coregulators  with  which  they  interact.  A  long-standing   research  aim  has  been  to define  the
mechanisms  by which Sp1-like  factors and KLFs  regulate gene expression  and cellular  function in
a  cell-  and  promoter-specific   manner.  Most  members  of  this  family   have  been  identified  in
mammals,  with at  least 21  Sp1-like/KLF  proteins encoded  in  the human  genome, and  members
are also  found  in frogs,  worms  and flies.  Sp1-like/KLF  proteins have  highly  conserved carboxy-
terminal  zinc-finger domains  that  function in  DNA binding.  The  amino terminus,  containing  the
transcription activation  domain, can vary significantly  between family  members.
Gene organization  and evolutionary history
Sp1 was identified in  the early 1980s 
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