2000
DOI: 10.1007/bf02759569
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Molecular phylogeny of theChironomus genus deduced from nucleotide sequences of two nuclear genes,ssp 160 and the globin 2b gene

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Cited by 14 publications
(10 citation statements)
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“…It seems unlikely that both groups show this similar pattern as a result of lineage sorting, whereas the presence of low levels of hybridization in both groups suggests gene flow as a more likely cause. This does not mean that mt gene flow will be common amongst Chironomus species, as our previous studies (Makarevich et al ., 2000; Guryev et al ., 2001) have revealed no obvious inconsistencies between mt and nuclear sequence data. There is also no evidence of mt gene flow between the two cryptic species included under the name C. calligraphus (Spies et al ., 2002).…”
Section: Discussionmentioning
confidence: 64%
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“…It seems unlikely that both groups show this similar pattern as a result of lineage sorting, whereas the presence of low levels of hybridization in both groups suggests gene flow as a more likely cause. This does not mean that mt gene flow will be common amongst Chironomus species, as our previous studies (Makarevich et al ., 2000; Guryev et al ., 2001) have revealed no obvious inconsistencies between mt and nuclear sequence data. There is also no evidence of mt gene flow between the two cryptic species included under the name C. calligraphus (Spies et al ., 2002).…”
Section: Discussionmentioning
confidence: 64%
“…4) are both consistent with the tree based on the gb2b sequences. There is further support for this tree from another nuclear gene, the ssp160 gene (Makarevich et al ., 2000). This gene is complete in C. pallidivittatus , in both the Nearctic and Palearctic, and in C. biwaprimus , while C. tentans (s.l.)…”
Section: Discussionmentioning
confidence: 81%
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“…Detailed genetic information, including cox1-RFLP sizes, the primers used to amplify the gb2β gene and whether or not the gb2β gene was amplified is given in Table 4. The gb2β gene of some Chironomus species includes an intron (type I or type II), whereas in others it is absent (Hankeln et al 1997;Makarevich et al 2000). This information is also given in Table 4.…”
Section: Species Delimitation and Identificationmentioning
confidence: 99%
“…The fragments of the vasa-related genes were amplified using degenerated primer pair VasFW and VasRV (Mochizuki et al, 2001). PCR was carried out in a volume of 30 ml using the standard technique with Taq polymerase at an annealing temperature of 48e55 C (Makarevich et al, 2000). Amplification products were separated in 1% agarose gel and then isolated using QIAquick Gel Extraction Kit (Qiagen) with subsequent subcloning into the pBluescript II SK vector and sequencing.…”
Section: Pcr Amplification Cloning and Sequencingmentioning
confidence: 99%