Template switching within exons 3 and 4 of K sub(V)11.1 (HERG) gives rise to a 5' truncated cDNA
K sub(V)11.1 (HERG) channels contribute to membrane potential in a number of excitable cell types. We cloned a variant of K sub(V)11.1 from human jejunum containing a 171bp deletion spanning exons 3 and 4. Expression of a full-length cDNA clone containing this deletion gave rise to protein that traf...
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Veröffentlicht in: | Biochemical and biophysical research communications 2006-07, Vol.345 (4), p.1342-1349 |
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creator | Ro, S Kang, SH Farrelly, A M Ordog, T Partain, R Fleming, N Sanders, K M Kenyon, J L Keef, K D |
description | K sub(V)11.1 (HERG) channels contribute to membrane potential in a number of excitable cell types. We cloned a variant of K sub(V)11.1 from human jejunum containing a 171bp deletion spanning exons 3 and 4. Expression of a full-length cDNA clone containing this deletion gave rise to protein that trafficked to the cell membrane and generated robust currents. The deletion occurred in a G/C-rich region and identical sequence elements of UGGUGG were located at the deletion boundaries. In recent studies these features have been implicated to cause deletions via template switching during cDNA synthesis. To examine this possibility we compared cDNAs from human brain, heart, and jejunum synthesized at lower (42 super(o)C) and higher temperatures (70 super(o)C). The 171bp deletion was absent at the higher temperature. Our results suggest that the sequence and secondary structure of mRNA in the G/C rich region leads to template switching producing a cDNA product with a 171bp deletion. |
doi_str_mv | 10.1016/j.bbrc.2006.05.032 |
format | Article |
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We cloned a variant of K sub(V)11.1 from human jejunum containing a 171bp deletion spanning exons 3 and 4. Expression of a full-length cDNA clone containing this deletion gave rise to protein that trafficked to the cell membrane and generated robust currents. The deletion occurred in a G/C-rich region and identical sequence elements of UGGUGG were located at the deletion boundaries. In recent studies these features have been implicated to cause deletions via template switching during cDNA synthesis. To examine this possibility we compared cDNAs from human brain, heart, and jejunum synthesized at lower (42 super(o)C) and higher temperatures (70 super(o)C). The 171bp deletion was absent at the higher temperature. Our results suggest that the sequence and secondary structure of mRNA in the G/C rich region leads to template switching producing a cDNA product with a 171bp deletion.</description><identifier>ISSN: 0006-291X</identifier><identifier>DOI: 10.1016/j.bbrc.2006.05.032</identifier><language>eng</language><ispartof>Biochemical and biophysical research communications, 2006-07, Vol.345 (4), p.1342-1349</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Ro, S</creatorcontrib><creatorcontrib>Kang, SH</creatorcontrib><creatorcontrib>Farrelly, A M</creatorcontrib><creatorcontrib>Ordog, T</creatorcontrib><creatorcontrib>Partain, R</creatorcontrib><creatorcontrib>Fleming, N</creatorcontrib><creatorcontrib>Sanders, K M</creatorcontrib><creatorcontrib>Kenyon, J L</creatorcontrib><creatorcontrib>Keef, K D</creatorcontrib><title>Template switching within exons 3 and 4 of K sub(V)11.1 (HERG) gives rise to a 5' truncated cDNA</title><title>Biochemical and biophysical research communications</title><description>K sub(V)11.1 (HERG) channels contribute to membrane potential in a number of excitable cell types. We cloned a variant of K sub(V)11.1 from human jejunum containing a 171bp deletion spanning exons 3 and 4. Expression of a full-length cDNA clone containing this deletion gave rise to protein that trafficked to the cell membrane and generated robust currents. The deletion occurred in a G/C-rich region and identical sequence elements of UGGUGG were located at the deletion boundaries. In recent studies these features have been implicated to cause deletions via template switching during cDNA synthesis. To examine this possibility we compared cDNAs from human brain, heart, and jejunum synthesized at lower (42 super(o)C) and higher temperatures (70 super(o)C). The 171bp deletion was absent at the higher temperature. 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We cloned a variant of K sub(V)11.1 from human jejunum containing a 171bp deletion spanning exons 3 and 4. Expression of a full-length cDNA clone containing this deletion gave rise to protein that trafficked to the cell membrane and generated robust currents. The deletion occurred in a G/C-rich region and identical sequence elements of UGGUGG were located at the deletion boundaries. In recent studies these features have been implicated to cause deletions via template switching during cDNA synthesis. To examine this possibility we compared cDNAs from human brain, heart, and jejunum synthesized at lower (42 super(o)C) and higher temperatures (70 super(o)C). The 171bp deletion was absent at the higher temperature. Our results suggest that the sequence and secondary structure of mRNA in the G/C rich region leads to template switching producing a cDNA product with a 171bp deletion.</abstract><doi>10.1016/j.bbrc.2006.05.032</doi></addata></record> |
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title | Template switching within exons 3 and 4 of K sub(V)11.1 (HERG) gives rise to a 5' truncated cDNA |
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