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Wells, C. D.

Publications and source records attributed to Wells, C. D..

2 recordsLinked to original sources

Embryogenesis, polyembryony, and settlement in the gorgonian Plexaura homomalla

Understanding the ontogeny and reproductive biology of reef-building organisms can shed light on patterns of population biology and community structure. This knowledge is particularly important for Caribbean octocorals, which seem to be more resilient to long-term environmental change than scleractinian corals and provide some of the same ecological services. We monitored the development of the black sea rod Plexaura homomalla, a common, widely distributed octocoral on shallow Caribbean reefs, from eggs to 3-polyp colonies over the course of 73 days. In aquaria on St John, U.S. Virgin Islands, gametes were released in spawning events three to six days after the July full moon. Cleavage started 3 hours after fertilization and was holoblastic, equal, and radial. Embryos were positively buoyant until becoming planulae. Planulae were competent after 4 days. Symbiodiniaceae began infecting polyps at around 8 days post fertilization. Development was typical for Caribbean octocorals, except for the occurrence of a novel form of asexual reproduction in octocorals: polyembryony. Fragmentation of embryos during development may represent a temporally varied tradeoff between number and size of propagules, in which large eggs have higher fertilization rates followed by polyembryony, which maximizes the number of surviving recruits by generating more, albeit smaller, larvae. Polyembryony may contribute to the success of some gorgonians on Caribbean reefs as other anthozoans are in decline.

developmental biology

Alternative transcription cycle for bacterial RNA polymerase

RNA polymerases (RNAPs) transcribe genes through a cycle of recruitment to promoter DNA, initiation, elongation, and termination. After termination, RNAP is thought to initiate the next round of transcription by detaching from DNA and rebinding a new promoter. We used single-molecule fluorescence microscopy to observe individual RNAP molecules after transcript release at a terminator. Following termination, RNAP almost always remained bound to DNA and sometimes exhibited one-dimensional sliding over thousands of basepairs. Unexpectedly, the DNA-bound RNAP often restarted transcription, usually in reverse direction, thus producing an antisense transcript. Furthermore, we report evidence of this \"secondary initiation\" in live cells, using genome-wide RNA sequencing. These findings reveal an alternative transcription cycle that allows RNAP to reinitiate without dissociating from DNA, which is likely to have important implications for gene regulation.

biophysics