Sequence of the cryptic satellite DNA from the plant Sinapis alba

A satellite DNA with a buoyant density equal to that of main band DNA in neutral cesium chloride (‘cryptic satellite’) can be isolated from the DNA of mustard (Sinapis alba) nuclei by Ag⁺/Cs₂SO₄ density gradient centrifugation. This satellite is cleaved into 172 bp repeat units by HinfI, AluI or HaeIII. The HinfI fragments have been further cleaved by AluI, and seven AluI subfragments have been sequenced. As a result two versions of a basic 172 HinfI repeat have been found, one (A + B) with an additional HinfI site. These two sequences (A + B and C) are the most frequent versions of the basic repeat of mustard satellite DNA. The basic 172 bp unit does not contain subrepeats or palindromic sequences. It is not similar (at a criterion of 15 common bases) with any known satellite sequence. It is not unusually highly methylated in the native state.     

Comparison of lag times in plant physiology

Abstract Comparison of lag (or latent) times is a useful tool in plant physiology for investigating potential mechanisms involved in a response. There are two main ways of deriving the lag time, but only one of these can be properly used for comparative purposes. The other method is biased by the faster responding plants and may not give a representative estimate for the lag time in the population. The fact that the two methods give different, non-comparable results has been widely overlooked. We suggest more care should be taken for their correct use, and propose two terms which can be used to describe the different estimates of the lag time to avoid confusion.