Path: utzoo!censor!geac!torsqnt!news-server.csri.toronto.edu!rutgers!usc!julius.cs.uiuc.edu!rpi!bu.edu!bu-bio!colby From: colby@bu-bio.bu.edu (Chris Colby) Newsgroups: sci.bio Subject: Re: Alu locations Keywords: alu sequences Message-ID: <70131@bu.edu.bu.edu> Date: 6 Dec 90 01:53:13 GMT References: <1965@fcs280s.ncifcrf.gov> Sender: news@bu.edu.bu.edu Reply-To: colby@bu-bio.UUCP (Chris Colby) Organization: Biology Dept., Bost Lines: 27 In article <1965@fcs280s.ncifcrf.gov> toms@fcs260c2.ncifcrf.gov (Tom Schneider) writes: >Hi everyone! > >A friend of mine, Doug Halverson, has cloned several pieces of human DNA and >has found that they don't all have Alu sequences in them. His question is, in >human genes that have been mapped or sequenced so far, have stretches of DNA as >long as 10 to 20 kb been found to be Alu free? Is this a trick question? Why don't you just do a restriction digestion with the enzyme Alu1 (for which the Alu site was named I'm led to believe). Look and see if you get any DNA larger than 20 kB. Of course since an Alu sequence is 300 bp long (I just opened my copy of Watson and looked it up) Alu1 will cut at some sites that are not Alu sequences. This is because Alu1 has a 4bp recognition sequence. Watson sez: Alu sequences are present in more than a million copies and represent 3 - 6 percent of the genome. Any 5000 bp segment will probably contain one because they are widely distributed. > Tom Schneider > National Cancer Institute > Laboratory of Mathematical Biology > Frederick, Maryland 21702-1201 > toms@ncifcrf.gov Chris Colby email: colby@bu-bio.bu.edu