Intra-specific rDNA-ITS restriction site variation and an improved protocol to distinguish species and hybrids in the Daphnia longispina complex

被引:14
|
作者
Skage, Morten
Hobek, Anders
Ruthova, Stepánka
Keller, Barbara
Petrusek, Adam
Sed'a, Jaromi R.
Spaak, Piet
机构
[1] Univ Bergen, Dept Biol, N-5007 Bergen, Norway
[2] Norwegian Inst Water Res, Reg Off Bergen, N-5817 Bergen, Norway
[3] Charles Univ Prague, Dept Ecol, CR-12844 Prague 2, Czech Republic
[4] Swiss Fed Inst Aquat Sci & Technol, Eawag, CH-8600 Dubendorf, Switzerland
[5] ETH, Inst Integrat Biol, CH-8092 Zurich, Switzerland
[6] Acad Sci Czech Republ, Inst Hydrobiol, Ctr Biol, Ceske Budejovice 37005, Czech Republic
关键词
Daphnia longispina species complex; ITS-RFLP; ribosomal DNA (rDNA); ITS; intragenomic; interspecific hybrids;
D O I
10.1007/s10750-007-9090-5
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
A collaborative research effort was undertaken to evaluate the robustness of a recently developed genetic tool for species identification of members in the morphologically variable Daphnia longispina species complex. This genetic method, based on restriction fragment length polymorphism (RFLP) of the internal transcribed spacer region (ITS) of nuclear ribosomal DNA (rDNA) with restriction enzymes Mwo I and Sau96 I [Billiones et al., 2004. Hydrobiologia 526: 43-53], was applied to many different European populations. Results were compared with two or more independently obtained characters (morphology, allozymes, mitochondrial DNA (mtDNA), or cloned rDNA-ITS sequences). Individuals of most taxa were readily identified, but unexpected ITS-RFLP patterns were found in many individuals indicated by other markers to be D. galeata or one of its hybrids. Among 43 investigated D. galeata populations (902 specimen analysed by ITS-RFLP), deviant RFLP fragment patterns occurred in 26 (i.e., more than half) of the populations. The deviant patterns could be attributed to the loss of one single restriction site in the ITS2 region. This loss made the distinction of D. galeata from other species unreliable, and F1 hybrids could not be identified. Future users should be aware of this shortcoming of the Billions et al. [2004. Hydrobiologia 526: 43-53] protocol. As a solution to this problem, we present an improved genetic identification protocol based on a simple double digestion of the rDNA-ITS region with the restriction enzymes BsrB I and EagI. Sequence analyses of rDNA-ITS clones and preliminary testing indicate that the new protocol is unaffected by the rDNA variation which troubled the Mwo I/Sau96 I protocol. Further, the new protocol identifies all European species of the D. longispina complex, as well as their F1 hybrids. However, a wider screening is required to verify its general utility for all species, since yet unknown variation may occur.
引用
收藏
页码:19 / 32
页数:14
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