Recent work has highlighted deep connections between sequence-length requirements for high-probability phylogeny reconstruction and the related problem of the estimation of ancestral sequences. In [Daskalakis et al.'09], building on the work of [Mossel'04], a tight sequence-length requirement was obtained for the CFN model. In particular the required sequence length for high-probability reconstruction was shown to undergo a sharp transition (from \(O(\log n)\) to \(\hbox{poly}(n)\), where \(n\) is the number of leaves) at the "critical" branch length \(\critmlq\) (if it exists) of the ancestral reconstruction problem. Here we consider the GTR model. For this model, recent results of [Roch'09] show that the tree can be accurately reconstructed with sequences of length \(O(\log(n))\) when the branch lengths are below \(\critksq\), known as the Kesten-Stigum (KS) bound. Although for the CFN model \(\critmlq = \critksq\), it is known that for the more general GTR models one has \(\critmlq \geq \critksq\) with a strict inequality in many cases. Here, we show that this phenomenon also holds for phylogenetic reconstruction by exhibiting a family of symmetric models \(Q\) and a phylogenetic reconstruction algorithm which recovers the tree from \(O(\log n)\)-length sequences for some branch lengths in the range \((\critksq,\critmlq)\). Second we prove that phylogenetic reconstruction under GTR models requires a polynomial sequence-length for branch lengths above \(\critmlq\).