TY - JOUR
T1 - Do nonasterid holoparasitic flowering plants have plastid genomes?
AU - Nickrent, Daniel L.
AU - Ouyang, Yan
AU - Duff, R. Joel
AU - DePamphilis, Claude W.
N1 - Funding Information:
We are grateful to Sherwin Carlquist for providing tissue samples of Hydnora and Wilhelm Barthlott for sending Cytinus. Help in locating Corynaea during field work in Costa Rica was generously provided by Jorge Gómez (Universidad de Costa Rica) and Luis Diego Gómez (R. & C. Wilson Botanical Garden). The laboratory assistance of Jamie Beam and Wei-xing Zong is gratefully acknowledged. Thanks go to Carl Woese for providing 16S rDNA primers that were used in our initial PCR experiments. Support for this project was provided by grants from the National Science Foundation (BSR-89-18385 and DEB 94-07984 to D.L.N.; DEB-91-20258 to C.W.D.) and an equipment grant from the N.I.H., the Special Research Program of the Office of Research Development and Administration, SIUC and the University Research Council of Vanderbilt University.
PY - 1997/7
Y1 - 1997/7
N2 - Past work involving the plastid genome (plustome) of holeparasitic plants has been confined to Scrophulariaceae (or Orobanchaceae) which have truncated plustomes owing to loss of photosynthetic and other genes. Nonasterid holeparasites from Balanophoraceae (Corynaea), Hydnoraceae (Hydnora) and Cytinaceae (Cytinus) were tested for the presence of plastid genes and a plastome. Using PCR, plastid 16S rDNA was successfully amplified and sequenced from the above three holoparasites. The sequence of Cytinus showed 121 single base substitutions relative to Nicotiana (8% of the molecule) whereas higher sequence divergence was observed in Hydnora and Corynaea (287 and 513 changes, respectively). Secondary structural models for these 16S rRNAs show that most changes are compensatory, thus suggesting they are functional. Probes constructed for 16S rDNA and for four plastid-encoded ribosomal protein genes (rps2, rps4, rps7 and rpl16) were used in Southern blots of digested genomic DNA from the three holoparasites. Positive hybridizations were obtained using each of the five probes only for Cytinus. For SmaI digests, all plastid gene probes hybridized to a common fragment ca. 20 kb in length in this species. Taken together, these data provide preliminary evidence suggestive of the retention of highly diverged and truncated plastid genome in Cytinus. The greater sequence divergence for 16S rDNA and the negative hybridization results for Hydnora and Corynaea suggests two possibilities: the loss of typically conserved elements of their plastomes or the complete absence of a plastome.
AB - Past work involving the plastid genome (plustome) of holeparasitic plants has been confined to Scrophulariaceae (or Orobanchaceae) which have truncated plustomes owing to loss of photosynthetic and other genes. Nonasterid holeparasites from Balanophoraceae (Corynaea), Hydnoraceae (Hydnora) and Cytinaceae (Cytinus) were tested for the presence of plastid genes and a plastome. Using PCR, plastid 16S rDNA was successfully amplified and sequenced from the above three holoparasites. The sequence of Cytinus showed 121 single base substitutions relative to Nicotiana (8% of the molecule) whereas higher sequence divergence was observed in Hydnora and Corynaea (287 and 513 changes, respectively). Secondary structural models for these 16S rRNAs show that most changes are compensatory, thus suggesting they are functional. Probes constructed for 16S rDNA and for four plastid-encoded ribosomal protein genes (rps2, rps4, rps7 and rpl16) were used in Southern blots of digested genomic DNA from the three holoparasites. Positive hybridizations were obtained using each of the five probes only for Cytinus. For SmaI digests, all plastid gene probes hybridized to a common fragment ca. 20 kb in length in this species. Taken together, these data provide preliminary evidence suggestive of the retention of highly diverged and truncated plastid genome in Cytinus. The greater sequence divergence for 16S rDNA and the negative hybridization results for Hydnora and Corynaea suggests two possibilities: the loss of typically conserved elements of their plastomes or the complete absence of a plastome.
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U2 - 10.1023/A:1005860632601
DO - 10.1023/A:1005860632601
M3 - Article
C2 - 9278163
AN - SCOPUS:0031193640
SN - 0167-4412
VL - 34
SP - 717
EP - 729
JO - Plant molecular biology
JF - Plant molecular biology
IS - 5
ER -